Recall archive
31,892 recalls · page 335 of 1329
Reported Jun 28, 2023
ICD-DR DDBB1D1 EVERA XT IS1/DF1 US, Model Number DDBB1D1; Implantable Cardioverter Defibrillators
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
119 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 28, 2023
TYR Anamix Early Years infant formula Net Wt. 14.1 oz (400g) UPC: 749735002186 Product is a powder packed metal cans. 6…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nutricia North America
FDA (openFDA food enforcement)
Reported Jun 28, 2023
Single Use Repositionable Clip QUICKCLIP PRO 165 CM 10/BX- Intended for hemostatic metal clip for the GI Tract Catalog…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 28, 2023
V-Sign Sensor 2, REF VS-A/P/N, a component of Sentec Digital Monitoring System (model SDMS).
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SenTec AG
FDA (openFDA device enforcement)
Reported Jun 28, 2023
ZIPRASIDONE HYDROCHLORIDE CAPSULES 20 mg, Unit Dose Carton 40 Capsules, Rx only, Mfd. By: Dr. Reddy's Laboratories…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories
FDA (openFDA drug enforcement)
Reported Jun 28, 2023
Hemospray Endoscopic Hemostat: Reference Part Numbers: a) HEMO-7, REF G56572; b) HEMO-7-EU, REF G24663;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wilson-Cook Medical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Consumer productsReported Jun 22, 2023
Havertys Recalls Concord Dual Power Recliner Chairs Due to Fall Hazard (Recall Alert)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Artistic Leathers S de RL de CV
CPSC
Consumer productsReported Jun 22, 2023
Infanttech Recalls Zooby Video Baby Monitors for Cars Due to Fire Hazard (Recall Alert)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Infanttech
CPSC
Consumer productsReported Jun 22, 2023
Boost The Mood Ceramic Mugs Recalled by Michael Giordano International Due to Fire Hazard
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Michael Giordano International Inc.
CPSC
Consumer productsReported Jun 22, 2023
Poseidon Diving Systems Recalls Poseidon M28A Dive Computers Due to Injury Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Poseidon Diving Systems Inc.
CPSC
Consumer productsReported Jun 22, 2023
Nationwide Pharmaceutical Recalls Iron Dietary Supplements Due to Failure to Meet Child Resistant Packaging…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Prodigy Innovation LLC
CPSC
Consumer productsReported Jun 22, 2023
Research Products Recalls Steam Humidifiers Due to Fire Hazard
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Research Products Corporation
CPSC
Consumer productsReported Jun 22, 2023
Sound Around Recalls Children's Multi-Purpose Helmets Due to Risk of Head Injury
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sound Around Inc.
CPSC
Consumer productsReported Jun 22, 2023
Zuru Recalls 7.5 Million Baby Shark and Mini Baby Shark Bath Toys With Hard Plastic Top Fins Due to Risk of Impalement,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Zuru LLC
CPSC
Reported Jun 21, 2023
Total Knee Pack, REF CETJ130, medical convenience kits
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.American Contract Systems, Inc.
FDA (openFDA device enforcement)
Reported Jun 21, 2023
Extended Phenytoin Sodium Capsules, USP, 100 mg, Rx Only, 100 capsules per bottle, Distributed by: Amneal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amneal Pharmaceuticals
FDA (openFDA drug enforcement)
Reported Jun 21, 2023
Lysteda (tranexamic acid) USP Tablets, 650 mg, 30 tablets per bottle, Rx Only, Manufactured for: Amring Pharmaceuticals…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Amring Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported Jun 21, 2023
Eye and Ear Dropper, Product Code 67082
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Apothecary Products, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 21, 2023
Tranexamic Acid USP Tablets, 650 mg, 30 tablets (3X10) Unit Dose, Rx Only, Manufactured for: AvKARE Pulaski, TN 38478,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Avkare LLC
FDA (openFDA drug enforcement)
Reported Jun 21, 2023
Driver Instrument, part of the Superion Indirect Decompression System, REF: 102-9800, used with the Superion Indirect…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Neuromodulation Corporation
FDA (openFDA device enforcement)
Reported Jun 21, 2023
Fresh Organic Freezer Strawberries Mexico with calyx (caps) removed, net wt. 18 lbs., packaged in a T60-800…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cascade International Foods, Inc.
FDA (openFDA food enforcement)
Reported Jun 21, 2023
Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Model Number 0998-00-0800-55, Part Number 0998-00-0800-XX
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Datascope Corp.
FDA (openFDA device enforcement)
Reported Jun 21, 2023
Tearaway Introducer Kit, REF: KIT-010-12, KIT-010-17, KIT-900-16
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Galt Medical Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 21, 2023
Exeter V40 Trial Head, 26mm, -3, Catalog Number 6364-8-026
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
FDA (openFDA device enforcement)
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