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FDA food · drug · device recalls, merged

Before you eat it, take it, or plug it in — check.

Big Nope pulls three separate FDA recall feeds into one list per state, so you’re not searching three government databases to get one answer.

Just announced

Straight from FDA press releases — not yet formally classified or risk-graded
UnclassifiedUndeclaredAnnounced September 4, 2026

Business Pill, Branch Manager for Mendietary supplements marketed for male sexual enhancement

Products contain undeclared yohimbine

Full report
Dietary SupplementsFood & Beverages

Recalling firm: SUPPLX.com

Grant-Valkaria, Florida - SUPPLX.com is voluntarily recalling Business Pill and Branch Manager for Men, products marketed as dietary supplements for male sexual enhancement, because FDA laboratory analysis confirmed that both products contain yohimbine that is not declared on the product labels.

Company contact: (321) 341-9501 · SupplxRecall@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced September 4, 2026

Foods AliveMoringa Leaf Powder

Potential to be contaminated with Salmonella

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Foods Alive Inc.

Foods Alive Inc of Angola, IN, is recalling its 8-ounce packages of organic moringa leaf powder because they have the potential to be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

B. Braun0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container

Presence of particulate matter identified as iron oxide

Full report
Drugs

Recalling firm: B. Braun Medical Inc.

“On September 3, 2026 firm updated their press release to include additional contaminants.” FOR IMMEDIATE RELEASE – September 3, 2026– Bethlehem, PA, B. Braun Medical Inc (B. Braun) is voluntarily recalling three (3) lots of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container, to the hospital/healthcare facility/user level due to presence of particulate matter identified as iron…

Company contact: recalls@bbraunusa.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced September 3, 2026

Great ValueOrganic Triple Berry Blend

Possible E. Coli Contamination

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Frutas y Hortalizas del Sur S.A.

September 02, 2026. Frutas y Hortalizas del Sur S.A., San Carlos, Chile expands its July 3, 2026, recall of frozen organic IQF blueberries to include one lot of Great Value frozen Organic Triple Berry Blend 10 OZ because of potential contamination with Escherichia coli O145:H28 (E. coli O145) .

Company contact: Info.foodsafety@comfrut.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

American Regent, Inc.Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial

Presence of particulate matter and lack of sterility assurance

Full report
Food & Beverages

Recalling firm: American Regent, Inc.

FOR IMMEDIATE RELEASE – September 3, 2026 – New Albany, OH, American Regent, Inc. is conducting a nationwide voluntary recall of three lots of Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vials to the consumer level. Customer complaints were received for leaking and cracked vials, resulting in lack of assurance of sterility.

View FDA’s announcement (opens in a new tab)
UnclassifiedUndeclaredAnnounced August 31, 2026

LipofitLipofit Extreme 2.0 Fat Burner Dietary Supplement

Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)

Full report
Dietary SupplementsDrugs

Recalling firm: Ana Salazar Modela Tu Cuerpo Inc.

FOR IMMEDIATE RELEASE - August 27, 2026 - Davie, Florida – Ana Salazar Modela Tu Cuerpo Inc. is recalling Lipofit Extreme Fat Burner 2.0, Lot 25M12F, expiration date 09/2027, to the consumer level.

Company contact: (954) 305-1004 · yandrydy@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced August 31, 2026

KofinasGarlic Mediterranean Infused Extra Virgin Olive Oil 500 ml, 250 ml, and 100 ml

Contains garlic essential oil not approved for culinary use

Full report
Food & BeveragesIngredients

Recalling firm: LMSI LLC

Cincinnati, OH (Aug. 29, 2026) - LMSI LLC/ Kofinas Olive Oil is issuing a voluntary recall of its Garlic Mediterranean infused extra virgin olive oil for using a garlic essential oil not approved for culinary use. The flavored oil was bottled in glass bottles in 500 ml, 250 ml, and 100 ml sizes.

View FDA’s announcement (opens in a new tab)
UnclassifiedAllergenUndeclaredAnnounced August 31, 2026

Little TemptationsChocolatey Eyeballs, 7 oz., 10 oz., 10.5 oz., 11 oz., and 16 oz.

Undeclared milk

Full report
Food & BeveragesAllergens

Recalling firm: Crystal Temptations

Crystal Temptations of North Arlington, NJ is recalling Halloween Chocolatey Eyeballs because they contain undeclared MILK allergens. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced August 29, 2026

Everything SproutsRobust Radish Mix, 5oz Cups

Potential to be contaminated with Shiga toxin-producing Escherichia coli (STEC) or Salmonella.

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Everything Sprouts, LLC

Everything Sprouts, LLC, based in Minneapolis, MN is expanding its voluntary recall of sprouts to include certain lots of Robust Radish Sprout Mix because it has the potential to be contaminated with Shiga toxin producing Escherichia coli (STEC) or Salmonella bacteria.

Company contact: everythingsproutsmn@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced August 29, 2026

MartinaMangoes

Potential contamination with Salmonella

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Panorama Produce

MAMARONECK, NY, AUG. 28, 2026 - Panorama Produce is recalling 302 boxes of size 9 (nine) mangoes because they may be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

Company contact: information@panoramaproduce.com

View FDA’s announcement (opens in a new tab)

Recalls nationwide

Data last updated: September 8, 2026 at 1:13 PM UTC

19,424 recalls found
Wording
UnclassifiedRisk not yet known
Medical deviceRecalled May 18, 2026

ProNephro AKI (NGAL) Reagent Kit (100 tests). IVD Acute Kidney Injury Test System.

The use of a non-validated rework process for assay reagents which could lead to missed diagnosis of renal disease, inappropriate treatment decisions, or inappropriate monitoring of renal disease in intended users.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
99266
Lot/product code:
Model number: ST101UB / 08787174 190; GTIN code: 5711435000156; Lot-number: 04909125 and 04912125.
Recalling firm:
Bioporto Diagnostics A/S
View official FDA record (opens in a new tab)
Class IIILow risk
DrugRecalled May 18, 2026

PRED MILD, prednisolone acetate ophthalmic suspension, USP, 0.12%, 10 mL, Sterile, Rx only, Allergen, Inc., an AbbVie company, North Chicago, IL 60064, Product of France, NDC 11980-174-10.

Failed Stability Specifications

ALL 50 STATES
Full report

A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.

Recall #:
D-0551-2026
Lot/product code:
Lot # 402805, 407596, Exp Date: 08/2026.
Recalling firm:
AbbVie Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 18, 2026

DeRoyal Industries Inc. Ref 46-406, Covaderm Plus, Vascular Access Dressing 6"x6" (15cmx15cm)

Sterile wound dressing, lacks sterility assurance

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
99044
Lot/product code:
Lot: 63295141/UDI: None
Recalling firm:
DeRoyal Industries Inc
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodBacteria/virusRecalled May 18, 2026

Legacy Tex Dressing Stabilizer Blend #7604-50, 50lb bags

Product tested positive for Salmonella

Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
H-1076-2026
Lot/product code:
Lot 26121A6A Item #502574 Use by 2027-05-04
Recalling firm:
International Food Products Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 18, 2026

Impella CP Set with SmartAssist. Product Codes: 1000080, 1000851, 0048-0014, 0048-0024-JP.

Exposure to the low purge pressure occurrence may result in persistent low purge pressure alarms and, in some cases, interruption or loss of mechanical circulatory support.

Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98946
Lot/product code:
GTIN: 00813502012279. Product Codes (Serial Number): 1000080 (677223, 672986, 673252, 644591, 645428, 644314, 613525), 1000851 (636173), 0048-0014 (499250), 0048-0024-JP (661216).
Recalling firm:
Abiomed, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodBacteria/virusRecalled May 18, 2026

Dairy House Ingredient Systems Strawberry Dairy Powder 05#5072-50, 50 lb bags

Potential for Salmonella

Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
H-1078-2026
Lot/product code:
Lot #26126A6A Use by 2027-05-06
Recalling firm:
International Food Products Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 18, 2026

Philips MultiDiagnost Eleva with the following Model Numbers: Model # 708032 for MultiDiagnost Eleva; Model # 708034 for MultiDiagnost Eleva with Flat Detector; Model # 708036 for MultiDiagnost Eleva; Model # 708037 for MultiDiagnost Eleva with Flat Detector; Model # 708038 for MultiDiagnost Eleva with Flat Detector.

Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended radiation exposure and additional contrast injection

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
99223
Lot/product code:
All codes
Recalling firm:
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled May 18, 2026

Vasopressin 2 Units/2 mL in 0.9% Sodium Chloride, syringe, IntegraDose Compounding Services, LLC. 3650 Victoria St N, Suite 900, Shoreview, MN, NDC 71139-0190-1.

Weaker than it should be Drug

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0593-2026
Lot/product code:
Lot#: 20260327VAS-3, BUD: 05/26/2026; 20260320VAS-3, BUD: 05/19/2026.
Recalling firm:
IntegraDose Compounding Services LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 18, 2026

Philips MultiDiagnost Eleva with the following Model Numbers: Model # 708032 for MultiDiagnost Eleva; Model # 708034 for MultiDiagnost Eleva with Flat Detector; Model # 708036 for MultiDiagnost Eleva; Model # 708037 for MultiDiagnost Eleva with Flat Detector; Model # 708038 for MultiDiagnost Eleva with Flat Detector.

Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended radiation exposure and additional contrast injection

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
99223
Lot/product code:
All codes
Recalling firm:
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled May 18, 2026

Raw Shelled Peanuts (Runner Type) 2,200 lb. Poly Tote Bags and 50kg Poly Bags

Not listed on the label Tree Nut Allergen

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0906-2026
Lot/product code:
Lot Numbers: 50520, 50647, 50519, 50521, 50522, 50777, 50748
Recalling firm:
Wilco Peanut Co
View official FDA record (opens in a new tab)
Class IIILow risk
DrugRecalled May 18, 2026

Lidocaine HCl Injection, USP 2%, 40 mg/2 mL (20 mg/mL), 2 mL per Single-Dose Vial, Rx Only, Mfd. in India for: Eugia US LLC, E. Windsor, NJ 08520. NDC: 55150-164-02

Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan

ALL 50 STATES
Full report

A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.

Recall #:
D-0552-2026
Lot/product code:
Lot, expiry: Lot 3LC26029A, exp Feb-2029; Lot 3LC26031A, exp Mar-2029
Recalling firm:
Eugia US LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 18, 2026

Philips Allura Xper with the following Model Numbers: Model # 722001 for Allura Xper FD10C; Model # 722002 for Allura Xper FD10F; Model # 722003 for Allura Xper FD10; Model # 722005 for Allura Xper FD10/10; Model # 722006 for Allura Xper FD20; Model # 722008 for Allura Xper FD20 Biplane; Model # 722010 for Allura Xper FD10; Model # 722011 for Allura Xper FD10/10; Model # 722012 for Allura Xper FD20; Model # 722013 for Allura Xper FD20 Biplane; Model # 722015 for Allura Xper FD20 OR Table; Model # 722019 for Allura Xper FD10/10 OR Table; Model # 722020 for Allura Xper FD20 Biplane OR Table; Model # 722022 for Allura Xper FD10 OR Table; Model # 722023 for Allura Xper FD20 OR Table; Model # 722025 for Allura Xper FD20 Biplane OR Table; Model # 722026 for Allura Xper FD10; Model # 722027 for Allura Xper FD10/10; Model # 722028 for Allura Xper FD20; Model # 722029 for Allura Xper FD20/10; Model #722033 for Allura Xper FD10 OR Table; Model #722035 for Allura Xper FD20 OR Table; Model #722038 for Allura Xper FD20/20; Model #722039 for Allura Xper FD20/20 OR Table; Model #722058 for Allura Xper FD20/15; Model #722059 for Allura Xper FD20/15 OR Table.

Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended radiation exposure and additional contrast injection

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
99223
Lot/product code:
All codes
Recalling firm:
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 18, 2026

GSP Neonatal GALT Kit. Product Codes: 3303-001U, 3303-0010. in vitro diagnostic. Used in FLUORESCENT PROC. (QUAL), GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE.

Reduction in the on-board stability of the GSP GALT assay. This may increase the likelihood of run-QC failures and consequently delay the reporting of patient results.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
99065
Lot/product code:
1. Product Code: 3303-001U. UDI-DI: 06438147321704. UDI-PI (PACKING LOT): (01)06438147321704(17)260531(10)763638 (1076363801); (01)06438147321704(17)260531(10)764085 (1076408501); (01)06438147321704(17)260531(10)765033 (1076503301); (01)06438147321704(17)260731(10)765231 (1076523101); (01)06438147321704(17)260731(10)765316 (1076531601); (01)06438147321704(17)261031(10)766420 (1076642001); (01)06438147321704(17)261031(10)766894 (1076689401); (01)06438147321704(17)261130(10)767873 (1076763801); (01)06438147321704(17)261130(10)768361 (1076836101); (01)06438147321704(17)261130(10)768703 (1076870301); (01)06438147321704(17)270228(10)769355 (1076935501); (01)06438147321704(17)270228(10)769542 (1076954201); (01)06438147321704(17)270228(10)769632 (1076963201); (01)06438147321704(17)270228(10)769671 (1076967101); (01)06438147321704(17)270228(10)769782 (1076978201); (01)06438147321704(17)270228(10)769871 (1076987101); (01)06438147321704(17)270228(10)769975 (1076997501); (01)06438147321704(17)270228(10)770078 (1077007801); (01)06438147321704(17)270228(10)770086 (1077008601); (01)06438147321704(17)270228(10)770351 (1077035101). 2. Product Code: 3303-0010. UDI-DI: 06438147311347. UDI-PI (PACKING LOT): (01)06438147311347(17)260531(10)763396 (1076339601); (01)06438147311347(17)260531(10)763396 (1076339602); (01)06438147311347(17)260531(10)764209 (1076420901); (01)06438147311347(17)260531(10)764209 (1076420902); (01)06438147311347(17)260731(10)765317 (1076531702); (01)06438147311347(17)260731(10)7653177 (1076531703); (01)06438147311347(17)261031(10)766378 (1076637801); (01)06438147311347(17)261031(10)766943 (1076694301); (01)06438147311347(17)261031(10)767323 (1076732301); (01)06438147311347(17)261130(10)767955 (1076795501); (01)06438147311347(17)261031(10)767956 (1076795601); (01)06438147311347(17)261130(10)769214 (1076921401); (01)06438147311347(17)261231(10)769967 (1076996701).
Recalling firm:
WALLAC OY
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 15, 2026

ALYON Surgical Lighting System

The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98768
Lot/product code:
UDIs: 00724995223182 00724995223137, 00724995223151, 00724995223175, 00724995222895, 00724995222994 00724995223014, 00724995223021, 00724995223083, 00724995223106, 00724995222758 00724995223120, 00724995223113, 00724995222840, 00724995223038, 00724995223076 00724995222987, 00724995223007, 00724995222703, 00724995222727, 00724995223090 00724995225711, 00724995225681, 00724995225698, 00724995225728, 00724995222826 00724995222802, 00724995222857, 00724995222697, 00724995222956, and 00724995223229
Recalling firm:
Steris Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 15, 2026

Reprocessed Electrophysiology Catheters and Ultrasound Catheters Item no. 401206RH, St. Jude Medical Response" Diagnostic Electrophysiology Catheter 4 Elec. 10mm; Item no. 401305RH, St. Jude Medical Response" Diagnostic Electrophysiology Catheter 10 Elec. 2-5-2mm.

Expansion of RES 98277. Specific lots of reprocessed catheters may contain small particles of residual material. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk of an inflammatory response or systemic infection. If particulate were to dislodge during use and contact circulating blood or the heart, it may produce a granulomatous reaction or thrombus formation, which may lead to cerebral or pulmonary embolism, or deep vein thrombosis.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
99122
Lot/product code:
Lot EP250203 Item no. 401206RH - UDI-DI 10197344043767; Item no. 401305RH - UDI-DI 10197344043637.
Recalling firm:
Medline Industries, LP
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodRecalled May 15, 2026

Great Value Hawaiian Roll 4pk, Item # F63384. Product is perishable dinner roll ready to eat, sold in a corrugated case of 18 packages (4.5oz net wt.) individually wrapped in laminated film. This product was never sold in stores and was never available for consumer purchase. All affected product remained at wholesale distribution centers and has been accounted for.

Firm observed oily and sticky substance on direct food contact surface packaging of finished product.

Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
H-0949-2026
Lot/product code:
W1 116 Julian Codes: 116 119 120 127 134 135 Dates of Production: 4/26/2026 4/29/2026 4/30/2026 5/7/2026 5/14/2026 5/15/2026
Recalling firm:
United States Bakery
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 15, 2026

HarmonyAIR A-Series Surgical Lighting System

The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98768
Lot/product code:
UDIs: 00724995185947, 00724995186418, 00724995187156, 00724995188009, 00724995188498, 00724995189198, 00724995185954, 00724995186425, 00724995187170, 00724995188016 00724995188504, 00724995189211, 00724995185961, 00724995186432, 00724995187187 00724995188047, 00724995188535, 00724995189228, 00724995185978, 00724995186548 00724995187217, 00724995188054, 00724995188542, 00724995189280,00724995185985, 00724995186555, 00724995187248, 00724995188078, 00724995188580, 00724995189372, 00724995186067, 00724995186562, 00724995187262, 00724995188122, 00724995188597, 00724995189419, 00724995186074, 00724995186579, 00724995187279, 00724995188221, 00724995188603, 00724995189990, 00724995186081, 00724995186593, 00724995187286, 00724995188238, 00724995188610, 00724995190002, 00724995186098, 00724995186616, 00724995187347, 00724995188245, 00724995188627, 00724995190033, 00724995186111, 00724995186623, 00724995187378, 00724995188252, 00724995188634, 00724995190040, 00724995186128, 00724995186661, 00724995187385, 00724995188269, 00724995188641, 00724995190354, 00724995186135, 00724995186678, 00724995187415, 00724995188276, 00724995188658, 00724995190361, 00724995186203, 00724995186685, 00724995187453, 00724995188283, 00724995188665, 00724995199364, 00724995186302, 00724995186692, 00724995187484, 00724995188290, 00724995188672, 00724995199913, 00724995186319, 00724995186722, 00724995187538, 00724995188306, 00724995188689, 00724995199944, 00724995186326, 00724995186739, 00724995187569, 00724995188313, 00724995188702, 00724995200480, 00724995186333, 00724995186746, 00724995187576, 00724995188320, 00724995188726, 00724995200886, 00724995186340, 00724995186753, 00724995187583, 00724995188337, 00724995188849, 00724995200909,00724995186357, 00724995186760, 00724995187606, 00724995188344, 00724995188948, 00724995200930, 00724995186364, 00724995186784, 00724995187620, 00724995188375, 00724995189068, 00724995200947, 00724995186371, 00724995186807, 00724995187712, 00724995188412, 00724995189075, 00724995200961, 00724995186388, 00724995186906, 00724995187729, 00724995188467, 00724995189105, 00724995201074, 00724995186395, 00724995187125, 00724995187989, 00724995188474, 00724995189136, 00724995217372, 00724995186401, 00724995187149, 00724995187996, 00724995188481, 00724995189181, 00724995222970
Recalling firm:
Steris Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 15, 2026

HarmonyAIR A-Series Surgical Lighting System

There is a potential for paint delamination (chipping/peeling) on the lighting system's light heads.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98767
Lot/product code:
UDIs: 00724995186388, 00724995186401, 00724995188320, 00724995188481, 00724995188467, 00724995188498, 00724995189433, 00724995186562, 00724995188696, 00724995188627, 00724995188610, 00724995186074, 00724995186081, 00724995186302, 00724995186319, 00724995188269, 00724995186371, 00724995188634, 00724995186326, 00724995186067, 00724995186548, 00724995186579, 00724995188580, 00724995187149, 00724995187170, 00724995187989, 00724995187644, 00724995188337, 00724995189297, 00724995188313, 00724995186128, 00724995188689, 00724995188252, 00724995188474, 00724995188597, 00724995188221, 00724995189174, 00724995188276, 00724995186180, 00724995189143 00724995186111, 00724995186340, 00724995187224, 00724995189075, 00724995188306 00724995188603, 00724995189051, 00724995200954, 00724995200022, 00724995199906 00724995190033, 00724995186678, 00724995188351, 00724995188665, 00724995187996 00724995189068, 00724995189099, 00724995189150, 00724995199869, 00724995187385 00724995187347, 00724995200886, 00724995190361, 00724995200893, 00724995200916 00724995186333, 00724995187026, 00724995187262, 00724995186715, 00724995186746 00724995188283, 00724995187279, 00724995186135, 00724995188511, 00724995188009, 00724995188245, 00724995189310, 00724995186555, 00724995188504, 00724995187033 00724995190354, 00724995188238, 00724995186739, 00724995188290, 00724995199890, 00724995187156, 00724995187187, 00724995187521, 00724995187552, 00724995186142, 00724995186647, 00724995185985, 00724995186104, 00724995187781, 00724995189334 00724995185954, 00724995186418, 00724995187217, 00724995189181, 00724995187415 00724995188030, 00724995189372, 00724995201128, 00724995189990, 00724995189235 00724995189204, 00724995200251, 00724995201135, 00724995200367, 00724995200343 00724995200114, 00724995200909, 00724995186357, 00724995188542, 00724995186173 00724995186661, 00724995200732, 00724995186807, 00724995200701, 00724995187569, 00724995186364, 00724995199401, 00724995186203, 00724995189198, 00724995190040 00724995186098, 00724995189136, 00724995189105, 00724995200329, 00724995188412, 00724995185978, 00724995186784, 00724995187712, 00724995188047, 00724995187088 00724995186685, 00724995186692, 00724995188641, 00724995186920, 00724995188658 00724995199388, 00724995200138, 00724995186500, 00724995199876, 00724995199364 00724995188672, 00724995188535, 00724995188122, 00724995186425, 00724995186616 00724995188375, 00724995187798, 00724995185947, 00724995186487, 00724995188016 00724995186753, 00724995188726, 00724995186166, 00724995199371, 00724995186906, 00724995188399, 00724995186449, 00724995189167, 00724995187231, 00724995187200 00724995187460, 00724995200770, 00724995200084, 00724995187576, 00724995187606 00724995200466, 00724995188108, 00724995186395, 00724995188054, 00724995189211 00724995200480, 00724995200947, 00724995189228, 00724995187620, 00724995189419 00724995201074, 00724995187125, 00724995188344, 00724995186623, 00724995188849 00724995200930, 00724995188078, 00724995188948, 00724995187286, 00724995187453 00724995199944, 00724995199913, 00724995186432, 00724995187484, 00724995187538 00724995190002, 00724995187248, 00724995188702, 00724995187378, 00724995185961 00724995186593, 00724995200961, 00724995189280, 00724995186722, 00724995186760 00724995187729, and 00724995187583; Serial Numbers: 0400224025 0402925005 0405124082 0407625017 0410525114 0413525005 0416725078 0419625227 0421623131 0423023296 0424625031 0426724199 0428824307 0431124255 0433724085 0400324053 0402925009 0405124092 0407625022 0410525120 0413525006 0416725082 0419625232 0421623135 0423023301 0424625032 0426824004 0428824308 0431225037 0433724089 0400324060 0402925023 0405124097 0407625025 0410525124 0413525008 0416725086 0419625237 0421623139 0423023332 0424625033 0426824008 0428923045 0431225041 0433724093 0400324064 0402925028 0405124102 0407625028 0410525128 0413525009 0416725091 0419625260 0421623143 0423023336 0424625034 0426825108 0428924044 0431225045 0433724097 0400324068 0402925033 0405124106 0407625031 0410525132 0413525022 0416725096 0419625264 0421623147 0423023340 0424725003 0426825109 0428924049 0431225049 0433724101 0400324072 0402925038 0405124110 0407625034 0410525136 0413525028 0416725099 0419625268 0421623151 0423023345 0424725006 0426825110 0428924075 0431225053 0433724105 0400324076 0402925041 0405124114 0407625037 0410525140 0413525029 0416924069 0419625272 0421623155 0423023350 0424923115 0426825111 0428924079 0431225057 0433724109 0400324080 0402925067 0405124119 0407625044 0410525146 0413525031 0416924074 0419625276 0421623159 0423023355 0424923118 0426825112 0428924083 0431225061 0433724113 0400424007 0402925071 0405124124 0407625048 0410525149 04135252002 0416924079 0419724105 0421623163 0423023360 0424923121 0426825113 0428925024 0431225065 0433724117 0400424011 0402925075 0405124128 0407625052 0410525153 0414025007 0416924084 0419724108 0421623167 0423023365 0424923146 0426825114 0428925028 0431225069 0433724121 0400424015 0402925079 0405124132 04076… (truncated, 48883 characters total — see the official FDA record for the full value)
Recalling firm:
Steris Corporation
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodRecalled May 15, 2026

DRAGONFLY Thai Ginger Powder Net Weight: 4.37 oz (125 g) PRODUCT OF THAILAND Packed for: U.S. Trading Company Hayward, CA 94545-1130 UPC: 721557533567

Potential contamination with lead.

Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
H-0943-2026
Lot/product code:
349MCF
Recalling firm:
U.S. Tov, Inc. dba U.S. Trading Company
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled May 15, 2026

VistaPharm, KERR INSTA-CHAR IN AN AQUEOUS BASE WITH CHERRY FLAVOR, 50 Grams Activated Charcoal in 240 ml (8 fl oz), distributed by: VistaPharm, Inc., Largo. FL 33771, NDC 66689-202-08.

Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0590-2026
Lot/product code:
Lot #: AE001, expires: 5/31/2026.
Recalling firm:
PAI Holdings LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled May 15, 2026

VistaPharm, KERR INSTA-CHAR IN AN SORBITOL BASE WITH CHERRY FLAVOR, 50 Grams Activated Charcoal in 52 Grams Sorbitol in 240 mL (8 fl oz), distributed by: VistaPharm, Inc., Largo. FL 33771, NDC 66689-203-08.

Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0592-2026
Lot/product code:
Lot #: AH001, expires: 8/31/2026
Recalling firm:
PAI Holdings LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled May 15, 2026

VistaPharm, KERR INSTA-CHAR IN AN AQUEOUS BASE WITH CHERRY FLAVOR, 25 Grams Activated Charcoal in 120 ml (4 fl oz), distributed by: VistaPharm, Inc., Largo. FL 33771, NDC 66689-202-04.

Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0589-2026
Lot/product code:
Lot #: AE001, expires: 5/31/2026.
Recalling firm:
PAI Holdings LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled May 15, 2026

VistaPharm, KERR INSTA-CHAR IN AN SORBITOL BASE WITH CHERRY FLAVOR, 25 Grams Activated Charcoal in 26 Grams Sorbitol in 120 mL (4 fl oz), distributed by: VistaPharm, Inc., Largo. FL 33771, NDC 66689-203-04.

Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0591-2026
Lot/product code:
Lot #: AE006, expires: 5/31/2026
Recalling firm:
PAI Holdings LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodForeign materialRecalled May 15, 2026

Ruby, Artichoke Hearts Quartered, 5 LB 8 OZ (2500 G) DRAINED WT 3 LBS 6 OZ (1550G), Can, 6 cans per case, Store in dry conditions .

Foreign material (Glass) was found in the product.

Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
H-1176-2026
Lot/product code:
P: 25/06/2026 BN: 186/2A E: 24/06/2028 Q.A NG
Recalling firm:
GELLERT GLOBAL GROUP
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 14, 2026

ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS12-100LPI. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.

Potential for overpressure alerts.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
98854
Lot/product code:
Catalog Number: iAS12-100LPI. UDI-DI: 10845854045640. Lot Numbers: 2025082210, 202502265, 202601074, 202512034, 202601084, 202512194, 202512184, 202512204, 202512224, 202512024, 2026010610, 2025100710, 202512094, 202512174, 2025121810, 202510214, 2026010511, 202510024, 202510104, 202510224, 202510084, 2025121710, 202510064, 202512104, 202512164, 202512064, 202512084, 202512054, 202512044, 202512154, 202510014, 202511144, 202511254, 202511264, 202510074, 202510144, 202511124, 202509094, 202509194, 202509294, 2025093010, 202509304, 202511134, 202511194, 202509084, 2025102310, 202510294, 202510304, 202510314, 202511046, 202511114, 2025101510, 202511154, 202511184, 202509184, 202510284, 202509174, 202511014, 202511044, 202511054, 202509044, 202509164, 202510274, 2025082210, 2025101310, 202509224, 2025092910, 202510134, 2025100610, 202508194, 202508234, 202509054, 202508184, 2025082110, 202508224, 202508144, 2025082010, 2025081110, 202508114, 202508134, 202508154, 202508054, 202508074, 2025080610, 202508254, 202507304, 202508064, 202507214, 202507224, 2025072410, 2025072510, 2025072810, 2025072910, 202507184, 202507284, 2025070910, 2025071010, 202507174, 202507154, 202507164, 2025072310, 2025071410, 2025070810, 202507084, 202507094, 202507144, 2025070710, 202507014, 202506234, 202507044, 2025070210, 202507024, 2025062310, 2025060610, 202506064, 2025060910, 202506094, 202506184, 2025060510, 202506054, 2025060410, 202507045, 202506044, 202506174, 202506034, 202506194, 2025062010, 202506204, 2025052210, 202505264, 2025050910, 202505104, 202506074, 2025061010, 202505204, 2025052110, 2025052310, 202505274, 2025050810, 202505084, 202505134, 2025051210, 202505224, 202505234, 2025052710, 202505094, 2025042910, 2025050710, 202505074, 202505214, 2025042810, 202505064, 202505124, 202504154, 202503194, 202504244, 202504254, 202504284, 202504114, 202504116, 202504144, 202504095, 202503125, 202503184, 202503185, 202502245, 202502255, 2025042210, 202503254, 202503265, 202502284, 202502285, 202503115, 202503276, 202503296, 202503274, 202503284, 202503314, 202503275, 202503286, 202503264, 202503266, 202503145, 202503255, 202503034, 202503035, 202503045, 202503055, 202503105, 2024121711, 202502134, 202502175, 202502135, 202502125, 202502184, 202502056, 202407174, 202411125, 202504015, 202509024, 202506126, 2025061910, 2025052610, 2025042510, 202504084, 202411304, 202412206, 202503256, 202509234, 2024111110, 202411166, 2024111811, 2024120511, 202412196, 202411054, 202411085, 202410174, 202411135, 202411296, 202412064, 202410164, 2024110611, 202409264, 202409134, 202411154, 202407276, 202407194, 202409175, 202409254, 202409135, 202408024, 202407235, 202407256, 202408235, 202406185, 202406186, 202407034, 202407085, 202407236, 2025062410, 2024111210, 202502195, 2024121810, 2024111810, 202407045, 202409184, 2024110810, 202509284, 202406276, 2025042410, 202503285, 202411115, 202412216, 2024110610, 202412034, 202410074, 202410184, 202410215, 2024110710, 202408085, 202407254, 202407055, 202407314, 202407095, 202502185, 202409194, 2025051310, 202511034, 202410155, 202409036, 202407316, 202505236, 202502215, 202407184, 202409304, 2024120411, 2024120311, 202408016, 202409195, 202412036, 2025081210, 202407035, 202408055, 2024121811, 202407195, 202501186 202410085, 202504294, 202502115, 202410224, 2024120410, 202509034, 202412056, 2024072510, 202409124, 202410025, 202407305, 202501096, 202411124, 202410154, 202407036, 202410024, 202407096, 202411185, 202407246, 202408086, 202407196, 202406275, 2026010710, 2024111510, 202412164, 202412035, 202407056, 202411155. OUS added 06/10/2026 expansion: 202412165, 2024121611, 2024110810, 202512164, 202512174, 202509174, 202510284, 202509304, 202508074, 202508194, 202508184, 202507304, 202506204, 2025062010, 202506174, 202506054, 2025060510, 202507174, 202507184, 202503296, 202503314, 2025042910, 202505074, 2025061010, 202506074, 202412026, 202411306, 202411284, 202503035, 202502245, 202412044, 202502284, 202410144, 202410114, 202408306, 202411114, 2024121710, 2024121711, 202501035, 202412195, 202412065, 202412054, 202511184, 202511044, 202511054, 202406275, 202406146, 202406175, 202409125, 202409135, 202407184, 202407185, 202407195, 202407194, 2025072910, 2025072310, 202504114, 2025050810, 202501075, 202411134, 202411145, 202407025, 202409024, 2025121810, 202506094, 202411074, 202508224, 202508054, 2025071410, 202507144, 202503284, 202504244, 2025060310, 202505104, 2025050910, 202504284, 202412035, 202501176, 202502265, 202501046, 202502125, 202411156, 2024121610, 2024111111, 2024121811, 202411185, 202410165, 202409305, 202410105, 202410024, 2024110710, 202412185, 202411085, 202412055, 202407036, 202407265, 202409205, 202407165, 202409124, 202409025, 202407094, 202507014, 2025042210, 202505084, 202512024, 202510024, 202512224, 2025100610, 202508234, 202511124, 202509294, 2025070710, 202503194, 202505094, 202502054, 202503034, 2024111510, 202410154, 202512054, 202407224, 202506064, 202512064, 202512194,… (truncated, 9378 characters total — see the official FDA record for the full value)
Recalling firm:
ConMed Corporation
View official FDA record (opens in a new tab)