Recall archive
31,892 recalls · page 249 of 1329
Reported May 22, 2024
Sterile CoFlex NL: Latex Free Flexible Cohesive Bandage, Tan, 4INx5YD (5400S)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Andover Healthcare Inc.
FDA (openFDA device enforcement)
Reported May 22, 2024
Spectrum IQ Infusion pump, Product Code 357009
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported May 22, 2024
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR3.5 (5PK), REF H74908526012; cardiac catheter
High riskUsing this product could cause serious injury, illness or death — stop using it now.Boston Scientific Corporation
47 more products in this recall
FDA (openFDA device enforcement)
Reported May 22, 2024
CardinalHealth Curity Flexible Adhesive Bandage X-Large 2 x 3.75 in. (5.1 x 9.5 cm), Model 44102, Sterile,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
FDA (openFDA device enforcement)
Reported May 22, 2024
Sysco Classic Riced Cauliflower packed in a 4lb plastic bag (6 units of 4 lb. per carton box).
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CN Frozen Foods, Inc.
FDA (openFDA food enforcement)
Reported May 22, 2024
EchoTip¿ Ultra HD Endoscopic Ultrasound Access Needle, ECHO-HD-19-A, G52012
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Medical Incorporated
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 22, 2024
County Road Seafood Inc. recalls County Road Seafood Crab Cake 2 Pack due to Potential or Undeclared Allergen - Egg
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.County Road Seafood Inc.
FDA (recalls & safety alerts)
Reported May 22, 2024
Gordofilm Wart Remover (salicylic acid 16.7% USP) packaged in 15 cc glass jars, Gordon Laboratories, Upper Darby PA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dercher Enterprises, Inc., dba Gordon Laboratories
FDA (openFDA drug enforcement)
Reported May 22, 2024
Organic Yogi Echinacea Immune Support, Caffeine Herbal Supplement, Serving Size 1 tea bag, 16 tea bags per pack, 4…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.East West Tea Company, LLC
FDA (openFDA food enforcement)
Reported May 22, 2024
Airvo 2 Humidifier, REF: PT101US, and myAirvo 2 Humidifier, REF: PT100US
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fisher & Paykel Healthcare, Ltd.
FDA (openFDA device enforcement)
Reported May 22, 2024
Novalung sensor box is a component of the Novalung Console (F30000162)-Indicated for long-term (> 6 hours) respiratory/…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Holdings, Inc.
FDA (openFDA device enforcement)
Reported May 22, 2024
HeartSine samaritan PAD (Public Access Defibrillator), Type: SAM 350P, SAM 360P, SAM 450P
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HeartSine Technologies Ltd.
FDA (openFDA device enforcement)
Reported May 22, 2024
1. Country Club, Price Chopper, Good & Gather, Hiland, Belfonte, Great Value, Hen House Vitamin D Whole Milk, 1 gallon.…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hiland Dairy Foods Company, LLC
FDA (openFDA food enforcement)
Reported May 22, 2024
Hospira Inc. recalls Hospira Buprenorphine Hydrochloride Injection Carpuject Units and Labetalol Hydrochloride Injection, USP Carpuject Units due to Device &…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Hospira Inc.
FDA (recalls & safety alerts)
Reported May 22, 2024
Infinite Herbs Organic Basil packed in a clear 2.5 oz, 2.0 oz, and 4 oz PET clamshell container.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Infinite Herbs, LLC
FDA (openFDA food enforcement)
Reported May 22, 2024
LASER Application Instrument, 23 cm, REF: 8694; LEUNIG-GREVERS LASER Application, REF: 461000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
FDA (openFDA device enforcement)
Reported May 22, 2024
Syntel Silicone Thrombectomy Catheter, Sterile, Rx Only. Used in vascular grafts and peripheral venous thrombectomies.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LeMaitre Vascular, Inc.
FDA (openFDA device enforcement)
Reported May 22, 2024
Cefdinir for Oral Suspension USP 250 mg/5 mL (60 mL when reconstituted), 60 mL bottle, Rx only, Manufactured for: Lupin…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lupin Pharmaceuticals Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported May 22, 2024
Jalapenos packed in 6lb 10oz cans. 6 cans per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.M-C McLANE INTERNATIONAL
FDA (openFDA food enforcement)
Reported May 22, 2024
Reagent Test Strips for Blood, Urobilinogen, Bilirubin, Protein, Nitrite, Ketones, Ascorbic Acid, Glucose, pH, Specific…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Macherey Nagel GmbH & Co. Kg
FDA (openFDA device enforcement)
Reported May 22, 2024
Losartan Potassium and Hydrochlorothiazide Tablets, USP 50mg /12.5 mg, 1000-count bottle, Rx only, Manufactured for:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Macleods Pharma USA, Inc.
FDA (openFDA drug enforcement)
Reported May 22, 2024
CARDIOHELP-i System. Blood oxygenation and carbon dioxide removal system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Medical Systems USA
FDA (openFDA device enforcement)
Reported May 22, 2024
APTUS 2.8 TriLock Screw 22mm, HD7, 1/Pkg. Metal bone fixation fastener used with the APTUS fixation system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medartis Inc.
FDA (openFDA device enforcement)
Reported May 22, 2024
namic CONVENIENCE KIT, a) CAROTID MANIFOLD KIT, REF 60011045; b) 3V MANIFOLD KIT ON WITH NAMIC DT & WASTE MANAGEMENT,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MEDLINE INDUSTRIES, LP - Northfield
1 more product in this recall
FDA (openFDA device enforcement)
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