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Recall archive

94,895 stored notices, from Jun 20, 2012 to Oct 14, 2026.

32,152 recalls · page 433 of 1340

Medical devices

Reported Jun 1, 2022

KWIK-STIK" plus: Clostridium perfringens

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Microbiologics Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 1, 2022

Mrs. Miller's Homemade Jam Smokey BBQ Bacon Jam packaged into 9 oz glass jar 12 jars per case

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Mrs Millers Homemade Jams LLC.

1 more product in this recall

FDA (openFDA food enforcement)

Drugs

Reported Jun 1, 2022

Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr) Contains: 30 Patches, Rx only,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Noven Pharmaceuticals Inc.

FDA (openFDA drug enforcement)

Food

Reported Jun 1, 2022

Wegmans Brand Fresh Goat Cheese, Classic Chevre, with Cranberries, 5.5lb; packaged in Cryovac Bags

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Old Chatham Sheepherding Creamery, LLC

FDA (openFDA food enforcement)

Drugs

Reported Jun 1, 2022

QM-4 Papaverine 30 mg/mL Phentolamine 3 mg/mL Alprostadil 300 mcg/mL Atropine 0.2 mg/mL, Multi-Dose 10 mL vial, Rx…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Olympia Compounding Pharmacy dba Olympia Pharmacy

52 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Jun 1, 2022

Olympus DISPOSABLE GRASPING FORCEPS, FG-51D

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Olympus Corporation of the Americas

FDA (openFDA device enforcement)

Drugs

Reported Jun 1, 2022

Losartan Potassium & HCTZ Tablets 50mg/12.5 mg, hydrochlorothiazide USP 12.5, Pkg Size: 90, NDC: 68788-7758-09.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Preferred Pharmaceuticals, Inc.

1 more product in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Jun 1, 2022

progenamatrix Human Keratin Matrix, sterile, Rx, with the following model numbers: (1) PM2012, 12 x 2 cm; (2) PM3002, 2…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ProgenaCare

FDA (openFDA device enforcement)

Drugs

Reported Jun 1, 2022

Losartan HCTZ 50/12.5 mg, 90 count bottle Original NDC# 33342-0050-10 Repackaged NDC# 70518-3231-00

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

RemedyRepack Inc.

2 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Jun 1, 2022

INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Right

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Smith & Nephew Orthopaedics GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Jun 1, 2022

Ultra Pure Non-Woven Sponges Non-Sterile 4-Ply 5,000 per case 25 sleeves of 200 2 in x 2 in / 5.1 cm x 5.1 cm Model…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Steris Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 1, 2022

Surgical Suture Kit

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stradis Healthcare

FDA (openFDA device enforcement)

Medical devices

Reported Jun 1, 2022

(1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile; (2) Gibeck Humid-Vent 2S Flex DC, Product #17732,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Teleflex Medical Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 1, 2022

AC-powered adjustable medical beds with built-in electric DC actuators and controls.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Umano Medical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported May 27, 2022

FSIS Issues Public Health Alert for Ready-to-Eat Salad Products Containing Peanut Butter that May be Contaminated with…

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

A G Specialty Foods

USDA FSIS

Food

Reported May 27, 2022

Albanese Confectionery Group, Inc. recalls Rich’s Peanut butter cups due to Salmonella

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Albanese Confectionery Group, Inc.

FDA (recalls & safety alerts)

Consumer products

Reported May 26, 2022

Asweets Recalls Wonder & Wise Activity Tables Due to Choking Hazard

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Asweets Global Inc., City

CPSC

Consumer products

Reported May 26, 2022

Copper Pearl Recalls Children's Sleepwear Due to Violation of Federal Flammability Standards and Burn Hazard

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Copper Pearl Inc.

CPSC

Consumer products

Reported May 26, 2022

Free Birdees Recalls Children's Pajamas Due to Burn Hazard (Recall Alert)

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Free Birdees LLC

CPSC

Medical devices

Reported May 25, 2022

Dragonfly OpStar Imaging Catheter, REF 1014651/1014652, 0.068 in, 0.014 in, 135 cm, STERILE EO

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Abbott Vascular

FDA (openFDA device enforcement)

Drugs

Reported May 25, 2022

Nitrofurantoin Capsules, USP (Monohydrate/Macrocrystals), 100 mg, 100 Capsules (10 x 10), 10-count blisters per card,…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

American Health Packaging

FDA (openFDA drug enforcement)

Drugs

Reported May 25, 2022

Sirolimus Oral Solution, 1 mg/mL, 60 mL bottle, Rx Only, Manufactured by: Apotex Inc. Toronto, Ontario Canada M9L 1T9…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Apotex Corp.

FDA (openFDA drug enforcement)

Food

Reported May 25, 2022

SE Grocers Cheesecake SAMPLER New York Style, Chocolate Silk, Strawberry Swirl, Turtle - NO ARTIFICIAL FLAVORS - NET WT…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Atlanta Cheesecake Company LLC

FDA (openFDA food enforcement)

Medical devices

Reported May 25, 2022

Atrium Advanta V12 Covered Stent System (OUS only). Product Code/Part Number: 85320 85321 85322 85323 85324 85325 85326…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Atrium Medical Corporation

1 more product in this recall

FDA (openFDA device enforcement)

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