Recall archive
32,164 recalls · page 456 of 1341
Reported Mar 1, 2022
FSIS Issues Public Health Alert for Ready-to-Eat Meat Products Containing FDA-Regulated Seasoning Mix That Has Been…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Fsis
USDA FSIS
Consumer productsReported Feb 24, 2022
Kelly Wynne Recalls Children's Handbags Due to Violation of Federal Lead Content Ban (Recall Alert)
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Kelly Wynne LLC
CPSC
Reported Feb 23, 2022
MAC DADDY RED Capsules, packaged in 10-count blisters per carton, ASIN B07TLDZLY2, UPC 742137 605191.
High riskUsing this product could cause serious injury, illness or death — stop using it now.ABC Sales 1 Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Feb 23, 2022
Alprazolam Tablets, USP 0.25 mg, packaged in a) 100-count bottles (NDC 67253-900-10), b) 500-count bottles (NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ANI Pharmaceuticals, Inc.
4 more products in this recall
FDA (openFDA drug enforcement)
Reported Feb 23, 2022
Moxifloxacin Ophthalmic Solution, USP 0.5% w/v, 3 mL bottle, Sterile, Rx Only, Distributed by: Aurobindo Pharma USA,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aurobindo Pharma USA Inc.
FDA (openFDA drug enforcement)
Reported Feb 23, 2022
RNAstill Molecular Transport Medium Vial, Catalog number MTM-001, a component of the following catalog numbers of…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Base 10 Genetics Inc.
FDA (openFDA device enforcement)
Consumer productsReported Feb 23, 2022
Bebe au Lait Recalls Teethers Due to Choking Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bebe au Lait
CPSC
Reported Feb 23, 2022
RED MAMMOTH capsules, 400 mg, packaged in 10-count blisters per carton, ASIN B00KA8FBNI, barcode X001ANE0I5.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Celebrate Today
FDA (openFDA drug enforcement)
Reported Feb 23, 2022
PARAGARD T380A (intrauterine copper contraceptive), 1 unit per carton together with an insertion tube and solid white…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CooperSurgical, Inc.
FDA (openFDA drug enforcement)
Reported Feb 23, 2022
Driscoll's Conventional Strawberries (Fresh) packed in 8x16oz clamshell and 4X32oz clamshell; 8 clamshells per case, 4…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Driscoll's Inc.
FDA (openFDA food enforcement)
Reported Feb 23, 2022
FLEXCERA BASE -a Dental resins for the fabrication of artificial teeth
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Envisiontec US LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 23, 2022
Steamable by Lidl Chopped Spinach NET WT 12 OZ (340 g) UPC 4 056489 34380 6. Frozen product.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Frozen Food Development Inc.
FDA (openFDA food enforcement)
Reported Feb 23, 2022
Enoki Mushrooms, brand Xuerong, net wt. 200g/7.05-ounce packages, UPC 6 953150 100684. Product sent to distributor is…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Golden Medal Mushroom Inc.
FDA (openFDA food enforcement)
Reported Feb 23, 2022
Liko Mobile Lifts: Primarily intended for use in nursing homes Liko M220, Model 2050010
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 23, 2022
Organic Roasted Salted Cashews, Net Weight of 6 oz (170g), UPC 6 16316 76283 1. Product is packed in a brown kraft…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Honey Heaven Wholesale Inc.
FDA (openFDA food enforcement)
Reported Feb 23, 2022
32MM -4 V40 TAPER VIT HEAD, Catalog Number 6260-5-032
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 23, 2022
365 SKINNY High Intensity Capsules, 600 mg, 30-count bottle, BODY BALANCE INTERNACIONAL
High riskUsing this product could cause serious injury, illness or death — stop using it now.Je Dois Lavoir LLC
FDA (openFDA drug enforcement)
Reported Feb 23, 2022
Diazepam Oral Solution (Concentrate), 25 mg per 5 mL (5 mg/mL), 30 mL BOTTLE and DROPPER, Rx Only, Distributed by:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lannett Company, Inc.
FDA (openFDA drug enforcement)
Reported Feb 23, 2022
Merete PediatrOS RigidTack, REF CP20120, Size 20 mm, Sterile, Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merete Medical GmbH
FDA (openFDA device enforcement)
Reported Feb 23, 2022
KWIK-STIK(TM), Quality control kit for culture media, sold as: KWIK-STIK(TM) 2-pack Enterococcus faecalis derived from…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Microbiologics Inc.
FDA (openFDA device enforcement)
Reported Feb 23, 2022
OER-Elite Endoscope Reprocessor-for use in cleaning and high-level disinfection of heat sensitive Olympus flexible…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Feb 23, 2022
NaturesPlus Advanced Therapeutics Glucosamine Chondroitin MSM Ultra Rx- Joint Cream, 4 oz tubes, Manufactured for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Organics Corporation
FDA (openFDA drug enforcement)
Reported Feb 23, 2022
Destino Twist 14F (also branded as Guidestar 14F)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oscor Inc.
FDA (openFDA device enforcement)
Reported Feb 23, 2022
Zenition 50, Model #718096
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems Nederland B.v.
2 more products in this recall
FDA (openFDA device enforcement)
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