Recall archive
32,165 recalls · page 473 of 1341
Reported Dec 8, 2021
NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System: Model Number/Item Number/Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NuVasive Specialized Orthopedics, Inc.
FDA (openFDA device enforcement)
Reported Dec 8, 2021
HALYARD STERLING ZERO NITRILE POWDER-FREE EXAM GLOVES, Sizes XS, S, M, L, and XL
Moderate riskThis product could cause temporary or reversible health problems — stop using it.O&m Halyard Inc.
FDA (openFDA device enforcement)
Reported Dec 8, 2021
5# (LB) Ctn (box) Jumbo Red Onions, Product of Mexico - Label Imperial Fresh Distributed by Carzalia Valley Produce,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Onions 52
2 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 8, 2021
5% Dextrose Injection, USP, 50 mL ADD-Vantage Unit, Rx only, Distributed by Hospira, INC., Lake Forest, IL 60045 USA,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pfizer Inc.
FDA (openFDA drug enforcement)
Reported Dec 8, 2021
TK006 Van Krimpet Powder Blend 50#. Item number 4107780
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Puratos Corporation (HQ and Innovation Center)
19 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 8, 2021
RANDOX CHOL-cholesterol (total) test system intended to measure cholesterol in plasma and serum REF: CH200
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories Ltd.
FDA (openFDA device enforcement)
Reported Dec 8, 2021
Enoxaparin Sodium Injection, USP, 40 mg/0.4 mL, Single-Dose Syringes with Automatic Safety Device, For Subcutaneous…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sandoz Inc.
FDA (openFDA drug enforcement)
Reported Dec 8, 2021
Dimension Vista 1500 In-vitro diagnostic device intended to duplicate manual analytical procedures such as pipetting,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 8, 2021
Abbott HeartMate Touch Communication System, REF: HMT1100 (US), HMT1100-R (Rental US), HMT1150 (EU)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec Corp.
FDA (openFDA device enforcement)
Reported Dec 8, 2021
Classic Irish Coffee Hint of Cocoa, each packet weighs 1.09 oz (31g), 30 packets per case. UPC 8 60003 91545 5. This…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trail Toddy & Company LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 8, 2021
INBONE Total Ankle System, INBONE POLY INSERT SZ 2 10mm SULCUS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wright Medical Technology Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Consumer productsReported Dec 6, 2021
Drive DeVilbiss Healthcare Recalls Adult Portable Bed Rails After Two Deaths; Entrapment and Asphyxiation Hazards
High riskUsing this product could cause serious injury, illness or death — stop using it now.Drive DeVilbiss Healthcare
CPSC
Reported Dec 5, 2021
Alexander & Hornung Recalls Fully Cooked Pork Products Due to Possible Listeria Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Alexander & Hornung
USDA FSIS
Reported Dec 3, 2021
Erie Meat Products Ltd. Recalls Chicken Bologna Products Imported Without Benefit of Inspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.Erie Meat Products Ltd.
USDA FSIS
Reported Dec 1, 2021
ARCHITECT i1000SR REF 01L86-01/1L86 and 1L87; ARCHITECT i2000SR REF 03M74-02/3M74; ARCHITECT i2000 REF 08C89-01/1G17…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 1, 2021
The Ocean Water Seal Chest Drain is a plastic, three bottle vacuum collection device. It consists of a collection…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Atrium Medical Corporation
FDA (openFDA device enforcement)
Reported Dec 1, 2021
Carvedilol Tablets, USP, 6.25 mg, 500 Tablets bottle, Rx Only, Distributed by: Aurobindo Pharma USA Inc., 279…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Aurobindo Pharma USA Inc.
FDA (openFDA drug enforcement)
Reported Dec 1, 2021
BD Nexiva, 20 GA 1.00 IN (1.1 X 25 mm), 3660 ml/hr. 61ml/min; Closed IV Catheter System- Dual port -61 mL/min (3660…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson Infusion Therapy Systems Inc.
FDA (openFDA device enforcement)
Reported Dec 1, 2021
Butalbital, APAP, Caf 50/325/40 Tablets, packaged in a) 12-count bottles, NDC: 63629-8392-09, barcode 083929152151; b)…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals
1 more product in this recall
FDA (openFDA drug enforcement)
Consumer productsReported Dec 1, 2021
E-filliate Recalls DEWALT Wireless Earphones Due to Burn and Fire Hazards
High riskUsing this product could cause serious injury, illness or death — stop using it now.E-filliate Inc.
CPSC
Reported Dec 1, 2021
Mr. Special Jugo de Pina De Concentrado, 46 oz cans, packaged cardboard boxes 12 cans per case of 46 oz each
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Empresas La Famosa, Inc.
FDA (openFDA food enforcement)
Reported Dec 1, 2021
Computed Tomography Systems Revolution CT, Revolution CT ES, Revolution Apex, Revolution CT with Apex edition
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Consumer productsReported Dec 1, 2021
Halo Recalls Promotional Children's Projector Flashlights Due to Button Battery Ingestion and Choking Hazards
High riskUsing this product could cause serious injury, illness or death — stop using it now.HALO Branded Solutions Inc.
CPSC
Reported Dec 1, 2021
HemosIL ReadiPlasTin (20 mL), Part number 0020301400. An in vitro diagnostic thromboplastin reagent.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumentation Laboratory
FDA (openFDA device enforcement)
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