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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 7, 2026 at 12:15 AM UTC

19,224 recalls found
Wording
Class IHigh risk
FoodRecalled November 21, 2025

Brass Pital Pot 4-quart. Sticker label: BRASS HAMMERED HANDI NO 3 UPC 7 023672 414398 US $ 74.99 Sticker label: IKM INDIAN KITCHEN MART

Potential contamination with leachable lead.

Full report

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

Recall #:
H-0514-2026
Lot/product code:
UPC: 7 023672 414398
Recalling firm:
Lotus Mom Corporation dba Indian Kitchen Mart
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled November 21, 2025

Pinna Grated Pecorino Romano 2/10, 10-pound plastic bags (units)

Product tested positive for Listeria Monocytogenes.

Full report

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

Recall #:
H-0369-2026
Lot/product code:
Lot number(s): 1000572486
Recalling firm:
Ambriola Co., Inc., The
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled November 21, 2025

Boar's Head Pecorino Romano Grated, 5-pound plastic bag (unit)

Product tested positive for Listeria Monocytogenes.

Full report

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

Recall #:
H-0372-2026
Lot/product code:
Lot number(s): 1000570093 1000570738
Recalling firm:
Ambriola Co., Inc., The
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled November 21, 2025

Locatelli Grated Pecorino Romano 4 oz and 8 oz plastic cup & lid, 12 units per case

Product tested positive for Listeria Monocytogenes.

Full report

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

Recall #:
H-0367-2026
Lot/product code:
Lot Numbers: 1000572472 1000570734 1000570735 1000570736 1000572482 1000572483 1000572485
Recalling firm:
Ambriola Co., Inc., The
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled November 21, 2025

Boar's Head Grated Pecorino Romano, 6 oz Plastic Cup & Lid, 12 units per case

Product tested positive for Listeria Monocytogenes.

Full report

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

Recall #:
H-0370-2026
Lot/product code:
Lot number(s): 1000572486
Recalling firm:
Ambriola Co., Inc., The
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled November 21, 2025

Ambriola Piccante grated Pecorino Romano, 5 and 10-pound plastic bags (units)

Product tested positive for Listeria Monocytogenes.

Full report

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

Recall #:
H-0373-2026
Lot/product code:
Lot number(s): 1000572981 1000570737 1000570092 1000572487
Recalling firm:
Ambriola Co., Inc., The
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled November 21, 2025

Sam's Pecorino Romano grated, 1.5 lb Plastic Bags, 12 units per case

Product tested positive for Listeria Monocytogenes.

Full report

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

Recall #:
H-0371-2026
Lot/product code:
Lot number(s): 1000570107 1000570766 1000572513
Recalling firm:
Ambriola Co., Inc., The
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled November 21, 2025

SENNA LEAVES F/C OG Item No: SEN15001 Net Wt: 44.75 Lbs Distributed By Whole Herb Company 19800 8th Street East, Sonoma, CA 95476 UPC 10031 44312

Potential contamination with Salmonella.

Full report

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

Recall #:
H-0325-2026
Lot/product code:
Lot No: 003279ST
Recalling firm:
The Whole Herb Company, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled November 21, 2025

Locatelli Grated Pecorino Romano, 5 and 10-pound plastic bags (units)

Product tested positive for Listeria Monocytogenes.

Full report

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

Recall #:
H-0368-2026
Lot/product code:
Lot numbers: 1000570725 1000572476 1000570724 1000572475 1000570726 1000570727 1000572477
Recalling firm:
Ambriola Co., Inc., The
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled November 8, 2025

1. ByHeart Whole Nutrition Infant Formula cans 24 OZ 680 grams; Cans sold in 1 pack, 2 packs, 4 packs, or 6 packs 2. ByHeart Whole Nutrition Infant Formula Anywhere Packs Single Serve Packet 17 grams in packages containing 14 Single Serve Packets

Contaminated with Clostridium botulinum

ALL 50 STATES
Full report

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

Recall #:
H-0249-2026
Lot/product code:
All batches and codes within expiry Finished Product Quantity 08NOV2023 to 08NOV2025 UPC Codes: Single Can: 8 50044 96800 8; Sams Club 2PK: 00850044968893; Amazon 2PK: 00850044968053; Anywhere pack: 8 50044 96802 2; 1-Count Sample Unit Anywhere Pack: 850044968015
Recalling firm:
ByHeart, INC.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled November 6, 2025

Famotidine Injection, USP, 20 mg per 2 mL (10 mg per mL), 2 mL vials, Rx only, Fresenius Kabi USA, LLC, NDC 63323-739-11 (unit of use), 63323-739-12 (unit of sale).

Microbial Contamination of Sterile Products; out of limit results obtained for endotoxin testing.

ALL 50 STATES
Full report

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

Recall #:
D-0182-2026
Lot/product code:
Lot #: 6133156, 6133194, Exp Date: 08/2026; 6133388, Exp Date: 10/2026.
Recalling firm:
Fresenius Kabi USA, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled November 5, 2025

Oven Dried Fish (SCOMBEROMORUS CAVALLA); distributed to walk-in customers of African Food on Wheels Inc. located at 1376 Randall Avenue, Bronx, NY 10474 only; Product is packed in a corrugated brown box.

Clostridium botulinum (uneviscerated fish)

Full report

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

Recall #:
H-0237-2026
Lot/product code:
No codes
Recalling firm:
African Food on Wheels Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodUndeclaredRecalled November 4, 2025

Sofit, Seedless Red Dates, 12 oz package, Plastic bags, 50 packages per case

Not listed on the label sulfites

Full report

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

Recall #:
H-0459-2026
Lot/product code:
Barcode: 4897056443990
Recalling firm:
Tai Phat Wholesalers, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled October 29, 2025

SiluetaYa Mexican Tejocote Roots Supplement Pieces; 7g/bottle; Dietary Supplement, UPC#: 7500464462411, Lot: US1220 " Expiration Date: 06/2027

Product contains yellow oleander

Full report

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

Recall #:
H-0647-2026
Lot/product code:
Lot: US1220, Expiration Date: 06/2027
Recalling firm:
Siluetaya, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled October 29, 2025

POTASSIUM CHLORIDE Inj., 20 mEq total in 50 mL Flexible Container, Highly concentrated 400 mEq/L, Rx Only, ICU Medical, Inc., Lake Forest, Illinois, 60045, USA, NDC# 0990-7077-14

Labeling: Label Error on Declared Strength-The overwrap label may incorrectly identify the product as POTASSIUM CHLORIDE Inj. 10 mEq instead of POTASSIUM CHLORIDE Inj. 20 mEq

ALL 50 STATES
Full report

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

Recall #:
D-0180-2026
Lot/product code:
Lot # 1030613, Exp Date: 09/30/2026
Recalling firm:
Otsuka ICU Medical LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled October 29, 2025

POTASSIUM CHLORIDE Inj., 10 mEq total in 100 mL Flexible Container, Highly concentrated 100 mEq/L, Rx Only, ICU Medical, Inc., Lake Forest, Illinois, 60045, USA, NDC# 0990-7074-26

Labeling: Label Error on Declared Strength-The overwrap label may incorrectly identify the product as POTASSIUM CHLORIDE Inj. 10 mEq instead of POTASSIUM CHLORIDE Inj. 20 mEq

ALL 50 STATES
Full report

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

Recall #:
D-0181-2026
Lot/product code:
Lot # 1030613, Exp Date: 09/30/2026
Recalling firm:
Otsuka ICU Medical LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled October 28, 2025

Dry Ghoinnya Fish

Un-eviscerated fish may be contaminated with Clostridia botulinum.

Full report

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

Recall #:
H-0202-2026
Lot/product code:
Expiration date of 5/19/25 UPC code is 908172635412.
Recalling firm:
New Hoque and Sons, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled October 24, 2025

Member's Mark Super Greens Dietary Supplement; 48 servings; Net Weight 18.28 oz (518.4g) UPC: 193968490775

Potential contamination of Salmonella Richmond

ALL 50 STATES
Full report

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

Recall #:
H-0205-2026
Lot/product code:
500-00055034; 500-00055035; 500-00055036; 500-00055037; 500-00055038; 500-00055039 500-00055040; 500-00055042; 500-00055043; 500-00055044; 500-00055045; 500-00055046 500-00055047; 500-00055048; 500-00055049; 500-00055050; 500-00055051; 500-00055052 500-00055053; 500-00055054; 500-00055055; 500-00055056; 500-00055057; 500-00055058 500-00056121; 500-00056122; 500-00056123; 500-00056124; 500-00056125; 500-00056126 500-00056127; 500-00056128; 500-00056129; 500-00056130; 500-00056131; 500-00056132 500-00056133; 500-00056134; 500-00056135; 500-00056136; 500-00056137; 500-00056138 500-00056139; 500-00056140; 500-00056141; 500-00056142; 500-00056143; 500-00056144 500-00056145; 500-00056146; 500-00056147; 500-00056148; 500-00056149; 500-00056150 500-00056151; 500-00056152; 500-00056153; 500-00056154; 500-00056155; 500-00056230 500-00056231; 500-00056318; 500-00056323; 500-00056429; 500-00056772;
Recalling firm:
MeriCal, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled October 20, 2025

SILINTAN 25/pills, packaged in a 25-count bottle, Shanghai Chinese Medical Works, Shanghai, China

Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of not listed on the label meloxicam.

ALL 50 STATES
Full report

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

Recall #:
D-0388-2026
Lot/product code:
All lots within expiry
Recalling firm:
ANTHONY TRINH, 123Herbals LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled October 8, 2025

Mojo Max Fusion XXX, 500 mg, one capsule per blister card, 20 count box, Distributed by: Max Nutrition Inc. UPC 6 78945 36675 0

Marketed Without an Approved NDA/ANDA-FDA analysis revealed not listed on the label sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule).

ALL 50 STATES
Full report

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

Recall #:
D-0396-2026
Lot/product code:
ALL LOTS, exp 12/31/2027
Recalling firm:
Mohamed Hagar
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled October 7, 2025

" Product Name: Pastured Grade AA Large Eggs " Product Description: Egg Carton, 12 eggs per dozen " Pack/Julian Date(s): Julian date 241(Aug 30) to 244 (Sep 2) and 246 (Sep 4) to 247 (Sep 5), Best by Dates 10/11 to 10/14/25 and 10/16 to 10/17.

Eggs may be contaminated with Salmonella.

Full report

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

Recall #:
H-0170-2026
Lot/product code:
Julian date 241(Aug 30) to 244 (Sep 2) and 246 (Sep 4) to 247 (Sep 5), Best by Dates 10/11 to 10/14/25 and 10/16 to 10/17.
Recalling firm:
Kenz Henz LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled September 27, 2025

Bona Fish

Fish is un-eviscerated (may be contaminated with Clostridia botulinum), is contaminated with mold, and contains filth (insect larvae)

Full report

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

Recall #:
H-0133-2026
Lot/product code:
no codes
Recalling firm:
Vicky IT Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled September 25, 2025

TAYLOR FARMS COOKED TROTOLLE MAP 8 X 2.75 lb pouches Net Weight: 22 lbs (9.97 kg) PERISHABLE KEEP REFRIGERATED

Potential contamination with Listeria monocytogenes.

Full report

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

Recall #:
H-0081-2026
Lot/product code:
Lot: 2532521, 2472524 USE BY: 10/10/2025, 10/04/2025
Recalling firm:
Nate's Fine Foods, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled September 25, 2025

FRESH CREATIVE FOODS COOKED PENNE PASTA 8 x 3 lb pouches Net Weight: 24 lbs (10.88 kg) PERISHABLE KEEP REFRIGERATED

Potential contamination with Listeria monocytogenes.

Full report

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

Recall #:
H-0077-2026
Lot/product code:
Lot: 2382521, 2452521, 2572524, 2512523 USE BY: 10/10/2025, 10/17/2025, 10/23/2025, 10/29/2025
Recalling firm:
Nate's Fine Foods, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled September 25, 2025

COOKED FETTUCCINE PASTA 6 X 5 lbs pouches Net Weight: 30 lbs (13.60 kg) PERISHABLE KEEP FROZEN

Potential contamination with Listeria monocytogenes.

Full report

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

Recall #:
H-0082-2026
Lot/product code:
Lot: 2572521 USE BY: 9/14/2026
Recalling firm:
Nate's Fine Foods, LLC
View official FDA record (opens in a new tab)