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Recalls affecting Minnesota

Data last updated: September 7, 2026 at 12:15 AM UTC

16,757 recalls found

Just announced

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

Business Pill, Branch Manager for Men — dietary 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 Alive — Moringa 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. Braun — 0.9% 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 Value — Organic 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

Lipofit — Lipofit 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

Kofinas — Garlic 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 Temptations — Chocolatey 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 Sprouts — Robust 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

Martina — Mangoes

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)
NewestOldest
High riskLow riskAll
Wording
Class IHigh risk
FoodBacteria/virusRecalled December 8, 2025

Sam Dry Fruits & Nuts PISTACHIO Meats Whole LOT #: PK00459 NET WEIGHT: 30 LBS PACK DATE: AUGUST/2025 EXPIRATION DATE: AUGUST/2027

Potential contamination with Salmonella.

ALL 50 STATES
▸Full report

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

Recall #:
H-0357-2026
Lot/product code:
LOT #: PK00459
Recalling firm:
Sam Dry Fruits and Nuts Enterprises, Inc
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
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
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
DrugRecalled September 16, 2025

Oxytocin 30 Units/500 mL in 0.9% Sodium Chloride for intravenous use, Rx only, IntegraDose Compounding Services LLC, 719 Kasota Ave Se, Minneapolis, MN 55414-2842 NDC 71139-0012-1

Weaker than it should be Drug: Testing revealed there was no oxytocin in the IV bag.

ALL 50 STATES
▸Full report

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

Recall #:
D-0015-2026
Lot/product code:
Lot #: 20250620OXY-1, Expiration date 10/18/2025
Recalling firm:
IntegraDose Compounding Services LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled September 10, 2025

GOODLES VEGAN IS BELIEVIN' PLANT-BASED WHITE CHEDDAR WITH SPIRALS NET WT 5.25 OZ (149g) INGREDIENTS: GOODLES SPIRALS (WHEAT FLOUR, CHICKPEA PROTEIN, WHEAT PROTEIN, NUTRIENTS EXTRACTED FROM [BROCCOLI, SPINACH, KALE, PUMPKIN, SWEET POTATO, SUNFLOWER SEED, CRANBERRY, CHLORELLA, MAITAKE MUSHROOM, SHIITAKE MUSHROOM]), VEGAN WHITE CHEDDAR CHEESE (DRIED CASHEW MILK [CASHEWS, CHICORY ROOT FIBER], NATURAL FLAVOR, NUTRITIONAL YEAST, TAPIOCA FLOUR, PEA PROTEIN, LACTIC ACID, DRIED APPLE CIDER VINEGAR, GARLIC). CONTAINS WHEAT AND CASHEWS Distributed by Gooder Foods Inc. Santa Cruz, CA 95060

Not listed on the label allergens (milk).

ALARAZCACOCTDCFLGAIAIDILINKSMAMDMEMIMNMOMTNCNHNJNYOHOKORPARISCTNTXUTVAWAWI
▸Full report

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

Recall #:
H-0027-2026
Lot/product code:
Lots: 09725N, 09825N, 09925N, 10025N, 10125N UPC: 850031990074 BEST IF USED BY: Jul-07-2026, Jul-08-2026, Jul-09-2026, Jul-10-2026, Jul-11-2026
Recalling firm:
Gooder Foods, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled September 10, 2025

GOODLES HERE COMES TRUFFLE CREAMY TRUFFLE FLAVORED CHEDDAR AND SHELLS NET WT 6 OZ (170g) INGREDIENTS: GOODLES SHELLS (WHEAT FLOUR, CHICKPEA PROTEIN, WHEAT PROTEIN, NUTRIENTS EXTRACTED FROM [BROCCOLI, SPINACH, KALE, PUMPKIN, SWEET POTATO, SUNFLOWER SEED, CRANBERRY, CHLORELLA, MAITAKE MUSHROOM, SHIITAKE MUSHROOM]), CHEDDAR AND PARMESAN CHEESES (CULTURED MILK, SALT, DISODIUM PHOSPHATE, ENZYMES), WHEY, NATURAL FLAVOR, BUTTER (CREAM, SALT), NONFAT DRY MILK, SALT, TAPIOCA FLOUR, NUTRITIONAL YEAST, LACTIC ACID, PORCINI MUSHROOMS, BLACK PEPPER, PAPRIKA, GROUND BALCK TRUFFLES. CONTAINS WHEAT AND MILK Distributed by Gooder Foods Inc. Santa Cruz, CA 95060

Not listed on the label allergens (cashews).

ALARAZCACOCTDCFLGAIAIDILINKSMAMDMEMIMNMOMTNCNHNJNYOHOKORPARISCTNTXUTVAWAWI
▸Full report

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

Recall #:
H-0028-2026
Lot/product code:
Lots: 10125 N, 10425 N, 10525 N UPC: 850031990159 BEST IF USED BY: Jul-11-2026, Jul-14-2026, Jul-15-2026
Recalling firm:
Gooder Foods, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled August 28, 2025

Green Lumber Natural Fuel For Men capsule, packaged in 2, 4, 10, and 30-count blister packs. GreenLumber.com, 2618 San Miguel Drive, Suite #296, Newport Beach, CA 92660

Marketed without an Approved NDA/ANDA: FDA analysis found this product to contain tadalafil

ALL 50 STATES
▸Full report

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

Recall #:
D-0304-2026
Lot/product code:
LOT308EXP03/28
Recalling firm:
Green Lumber Holdings, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled August 27, 2025

Cyclobenzaprine Hydrochloride Tablets, USP, 10 mg, 90-count bottle, RX only, Manufactured by: Unichem Laboratories, Ltd, Pilerne Ind. Estate, Pilerne, Bardez, Goa, India; Manufactured for: Unichem Pharmaceuticals (USA), Inc. East Brunswick, NJ. NDC 29300-415-19.

Labeling: Label Mix Up; Bottles of Meloxicam USP, 7.5mg, 90-count tablets (yellow in color), were labeled as Cyclobenzaprine Hydrochloride Tablets USP, 10 mg 90-count tablets (blue in color).

ALL 50 STATES
▸Full report

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

Recall #:
D-0655-2025
Lot/product code:
Lot No: GMML24026A, Expires: 09/30/2027
Recalling firm:
Unichem Pharmaceuticals USA Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled August 18, 2025

0.9% Sodium Chloride Injection USP, 1000 mL container, Rx only, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-7800-09

Presence of Particulate Matter.

ALL 50 STATES
▸Full report

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

Recall #:
D-0628-2025
Lot/product code:
Lot #: V3K770, Exp 1/31/2026
Recalling firm:
B BRAUN MEDICAL INC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled August 18, 2025

Lactated Ringers's Injection USP, 1000 mL container, Rx only, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-7750-07

Presence of Particulate Matter

ALL 50 STATES
▸Full report

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

Recall #:
D-0627-2025
Lot/product code:
Lot #: J4S807, Exp 5/31/2027
Recalling firm:
B BRAUN MEDICAL INC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled July 30, 2025

NAD+ (Nicotinamide adenine dinucleotide) for Injection, a) 100 mg/mL b) 200 mg/mL, 10 mL multi-dose amber vials, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.

Microbial Contamination of Sterile Products: elevated endotoxin levels

ALL 50 STATES
▸Full report

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

Recall #:
D-0094-2026
Lot/product code:
Lot#: GG121624-023, within expiry
Recalling firm:
GenoGenix LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled July 25, 2025

Member's Mark FREEZE DRIED FRUIT VARIETY PACK 15 COUNT 5-0.35OZ (10g) STRAWBERRY POUCHES 5-0.42OZ (12g) BANANA POUCHES 5-0.25 OZ (10g) APPLE POUCHES NET WT 5.6OZ (160g) NO ADDED SWEETENERS ONE INGREDIENT ONLY PER PACK UPC 1 93968 50900 2

Listeria monocytogenes. During routine testing the firm received positive test results for Listeria monocytogenes.

ALARAZCACOCTDEFLGAHIIAIDILINKSLAMDMEMIMNMOMSMTNCNDNENHNJNMNVNYOHOKPAPRSCSDTNTXUTVAWIWVWY
▸Full report

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

Recall #:
H-0394-2025
Lot/product code:
Best By: 06/24/2027 25175; Best By: 06/25/2027 25176; Best By: 06/26/2027 25177; Best By: 06/30/2027 25181; Best By: 07/01/2027 25182; Best By: 07/02/2027 25183; Best By: 07/03/2027 25184; Best By: 07/05/2027 25186; Best By: 07/07/2027 25188; Best By: 07/08/2027 25189; Best By: 07/09/2027 25190; Best By: 07/10/2027 25191; Best By: 07/11/2027 25192; Best By: 07/15/2027 25196; Best By: 07/16/2027 25197; Best By: 07/27/2027 25198; Best By: 07/18/2027 25199; Best By: 07/21/2027 25202; Best By: 07/22/2027 25203; Best By: 07/23/2027 25204; Best By: 07/24/2027 25205; Best By: 07/25/2027 25206
Recalling firm:
Doehler North America, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled July 17, 2025

DermaKleen, Health Care Antiseptic Lotion Soap with Vitamin E (Chloroxylenol 0.2%), packaged in a) 800 ml (27 fl. oz.) bag-n-box (NDC 61924-092-27) and b) 1000ml (34 fl. oz.) bag-n-box (NDC 61924-092-34) , DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.

ALL 50 STATES
▸Full report

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

Recall #:
D-0610-2025
Lot/product code:
Lot # and Expiration Date: a) 30550A, Exp. Date 7/2025; 30670A, 30682A, Exp. Date 8/2025; 40025A, Exp. Date 1/2026; 40375A, Exp. Date 4/2026; 40427A, 40436A, Exp. Date 5/2026; 50068A, Exp. Date 1/2027. b)30586A, 30586B, 30626A, Exp. Date 7/2025; 30628A, 30657A, Exp. Date 8/2025; 30741A, Exp. Date 7/2025; 30871A, Exp. Date 10/2025; 40002A, Exp. Date 12/2025; 40012A, Exp. Date 1/2026; 40301A, Exp. Date 3/2026; 40789 A, Exp. Date 9/2026; 50068B, Exp. Date 1/2027; 50144A, 50149A, Exp. Date 2/2027.
Recalling firm:
DermaRite Industries, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled July 17, 2025

PeriGiene, Health Care Antiseptic, (Chloroxylenol 0.5%) 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-198-08

Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.

ALL 50 STATES
▸Full report

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

Recall #:
D-0613-2025
Lot/product code:
Lot #: 31013A, Exp. Date 11/2025; 40345A, 40355A, Exp. Date 4/2026; 40571A, 40580A, Exp. Date 6/2026; 40587A, 40591A, Exp. Date 7/2026; 40870.1, 40877.1, Exp. Date 10/2026; 41093A, Exp. Date 12/2026; 50072A, 50079A, Exp. Date 1/2027
Recalling firm:
DermaRite Industries, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled July 17, 2025

KleenFoam, Antimicrobial Foam Soap with Aloe Vera, (Chloroxylenol 0.5%) 34 FL OZ (1000 mL) per cartridge, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-093-34

Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.

ALL 50 STATES
▸Full report

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

Recall #:
D-0612-2025
Lot/product code:
Lot #: 30705A, Exp. Date 8/2025; 30771A, Exp. Date 9/2025; 30920A, Exp. Date 10/2025; 40016A, Exp. Date 1/2026; 40303A, Exp. Date 4/2026; 40428A, Exp. Date 5/2026; 40505A, Exp. Date 6/2026; 41053C, 41053A, 41053B, Exp. Date 12/2026, 50017A, Exp. Date 1/2027.
Recalling firm:
DermaRite Industries, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled July 17, 2025

DermaSarra, External Analgesic, (Camphor 0.5%) 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-189-08

Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.

ALL 50 STATES
▸Full report

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

Recall #:
D-0611-2025
Lot/product code:
Lot #: 40187.2, Exp. Date 2/2026
Recalling firm:
DermaRite Industries, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled July 14, 2025

Dubai emek SPREAD PISTACHIO CACAO CREAM WITH KADAYIF NET WT. 9.7oz UPC 8 69652 10130 1 Manufacturer: Emek Dogal Saglik Urunlerilkl. Gida Turkey

Salmonella. The firm was notified by the FDA that the product may be contaminated with Salmonella.

ALAZCACOCTFLGAIAILINKSKYLAMAMDMIMNMONCNENHNJOHOKPASCSDTNTXVAWAWI
▸Full report

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

Recall #:
H-0305-2025
Lot/product code:
BEST BEFORE: APRIL 01 2027; BATCH NUMBER: 250401
Recalling firm:
World Market Management Services, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled July 10, 2025

FANCY MEDIUM PECAN PIECES 81124 561958 554707 6/13/2025 SDC1645 90 FANCY MEDIUM PECAN PIECES 81124 561965 554714 6/13/2025 SDC1645 90 FANCY MIDGET PECAN PIECES 81086 561845 554594 5/30/2025 SDC1505 56 FCY #15 HLVS 79291 561943 554692 5/21/2025 SDC1405 56 FANCY SMALL PECAN PIECES 81014 562088 554838 5/29/2025 SDC1495 56 FANCY SMALL PECAN PIECES 81014 562201 554951 5/29/2025 SDC1495 56 FANCY JR. MAMMOTH PECAN HALVES 81035 563565 556583 6/11/2025 SDC1625 6 FCY #15 HLVS 79291 562099 554849 5/21/2025 SDC1405 56 FCY #15 HLVS 79291 562100 554850 5/21/2025 SDC1405 32 FANCY JR. MAMMOTH PECAN HALVES 80801 561900 554649 6/5/2025 SDC1565 56 FANCY TOPPER PECAN HALVES 81165 562025 554774 5/30/2025 SDC1505 28 FANCY TOPPER HLVS/MED PCS BLEND 81070 562029 554778 5/28/2025 SDC1505 56 FANCY TOPPER HLVS/MED PCS BLEND 81072 562160 554910 6/10/2025 SDC1615 56 FANCY TOPPER HLVS/MED PCS BLEND 81072 562161 554911 6/10/2025 SDC1615 56 FANCY TOPPER HLVS/MED PCS BLEND 81072 562162 554912 6/10/2025 SDC1615 56 FANCY MEDIUM PECAN PIECES 81162 562058 554808 5/16/2025 UPS 7 FANCY JUMBO PECAN HALVES 81162 562059 554809 5/16/2025 UPS 3 FANCY EX-LRG/JUMBO PECAN HALVES 80991 561931 554680 5/19/2025 SDC1395 1500 FANCY LARGE PECAN PIECES 81160 561970 554719 5/15/2025 CP 4 FANCY SMALL PECAN PIECES 81163 562024 554773 5/22/2025 SDC1495 1 FANCY MEDIUM PECAN PIECES 81163 562060 554810 5/22/2025 CP 2 FANCY SMALL PECAN PIECES 81014 561940 554689 5/29/2025 SDC1495 56 FANCY SMALL PECAN PIECES 81014 561945 554694 5/29/2025 SDC1495 56 FANCY SMALL PECAN PIECES 81014 561982 554731 5/29/2025 SDC1495 56 FANCY SMALL PECAN PIECES 81014 561988 554737 5/29/2025 SDC1495 56 FANCY SMALL PECAN PIECES 81014 562020 554769 5/29/2025 SDC1495 56 FANCY SMALL PECAN PIECES 81014 562035 554784 5/29/2025 SDC1495 56

Pecans have the potential to be contaminated with Salmonella,

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

Recall #:
H-0379-2025
Lot/product code:
561958; 561965; 561845; 561943; 562099; 562100; 561900; 562025; 562029; 562160; 562161; 562162; 562058; 562059; 561931; 561970; 562024; 562060; 561940; 561945; 561982; 561988; 562020; 562035; 562088; 562201; 563565
Recalling firm:
Navarro Pecan Holdings, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled June 27, 2025

Buffered Penicillin G Potassium for Injection, USP 20,000,000 Units (20 million units), For IV use, Sterile, Rx Only, Manufactured in Austria by Sandoz GmbH for Sandoz Inc. Princeton, NJ 08540, NDC: 0781-6136-94.

Labeling: Label Mix-Up; Some vials of Cefazolin for Injection, USP 1 gram were incorrectly labeled as penicillin G potassium for Injection, USP, 20 million Unit

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

Recall #:
D-0570-2025
Lot/product code:
Lot # PG4360, PG4362, Exp. 11/30/2027
Recalling firm:
Sandoz Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled June 27, 2025

Cefazolin for Injection, USP, 1 gram per vial, Sterile, For Intramuscular or Intravenous Use, Rx Only, Manufactured by Sandoz GmbH for Sandoz Inc. Princeton, NJ 08540, NDC: 0781 3451-70 (vial), NDC: 0781-3451-96 (carton).

Labeling: Label Mix-Up; cartons of Cefazolin for Injection, USP 1 gram were found to contain vials labeled as penicillin G potassium for Injection, USP, 20 million Unit. The vials contained Cefozalin

ALL 50 STATES
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The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0569-2025
Lot/product code:
Lot # PG4360, PG4362, Exp. 11/30/2027
Recalling firm:
Sandoz Inc
View official FDA record (opens in a new tab)