Recall archive
31,892 recalls · page 353 of 1329
Reported Apr 12, 2023
VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System, Model Number C-VH-3500
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Cardiovascular, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 12, 2023
Medtronic Grafton Putty: a) DBM S43101 GRAFTON 0.5CC PUTTY, REF S43101; b) DBM S43102 GRAFTON 1CC PUTTY, REF S43102; c)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Sofamor Danek USA Inc.
11 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 12, 2023
Moberg Component Neuromonitoring System (CNS Monitor)-Intended as a short-term neurological monitoring system that…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Moberg Research, Inc.
FDA (openFDA device enforcement)
Reported Apr 12, 2023
Gerber GoodStart SoothePro Infant Formula with Iron. Milk Based Powder. Stage 1, 0 - 12 Months. Nestle Infant…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Perrigo Nutritionals
FDA (openFDA food enforcement)
Reported Apr 12, 2023
Trilogy Evo O2 and LifeVentEVO2 Portable Electric Ventilator, Model Numbers DS2100X11B, IN2100X15B, IN2100X19,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Philips Respironics, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 12, 2023
Alprazolam Tab, USP 0.25mg, (CIV), 30-count bottle, Rx Only, Preferred Pharmaceuticals, Inc. Manufactured by:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Preferred Pharmaceuticals, Inc.
19 more products in this recall
FDA (openFDA drug enforcement)
Reported Apr 12, 2023
Aripiprazole 5mg tablets, 30-count bottles, Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701, NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RemedyRepack Inc.
13 more products in this recall
FDA (openFDA drug enforcement)
Reported Apr 12, 2023
Tempus Pro Patient Monitor is a portable vital signs monitor intended to be used by clinicians and medically qualified…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remote Diagnostic Technologies Ltd.
FDA (openFDA device enforcement)
Reported Apr 12, 2023
Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 30X4,1BLA,1PRT QUICK Catalog number: 5921-030-135NS…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Corporation
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 12, 2023
CAPIOX RX15 Hollow Fiber Oxygenator, Catalog Number 3CX*RX15RE30
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 12, 2023
Montelukast Sodium Oral Granules USP, 4 mg, packaged in a carton containing 30 packets, Rx only, Distributed By: Teva…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teva Pharmaceuticals USA Inc.
FDA (openFDA drug enforcement)
Reported Apr 12, 2023
Sysco Imperial Caesar Dressing NET CONTENTS 1 GAL (3.78 l) INGREDIENTS: Soybean Oil, Water, Distilled Vinegar, Parmesan…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Winland Foods, Inc.
FDA (openFDA food enforcement)
Reported Apr 12, 2023
FURIKAKE SEASONED ROASTED SEAWEED FLAKES SEAFOOD Product number: 38245 Brand name: Shirakiku Distributed by: Wismettac…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Wismettac Asian Foods, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 7, 2023
Fresh Express Incorporated recalls Fresh Express & Publix Salad Kits due to Listeria monocytogenes
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Fresh Express Incorporated
FDA (recalls & safety alerts)
Reported Apr 7, 2023
FSIS Issues Public Health Alert for Fresh Salads With Chicken and Ham Containing Lettuce Recalled by FDA for Possible…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Russ' Commissary
USDA FSIS
Consumer productsReported Apr 6, 2023
BISSELL Expands Recall of Cordless Multi-Surface Wet Dry Vacuums Due to Fire Hazard
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.BISSELL Homecare Inc.
CPSC
Consumer productsReported Apr 6, 2023
IKEA Recalls BLÅVINGAD Fishing Games Due to Choking Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.IKEA Supply AG
CPSC
Consumer productsReported Apr 6, 2023
Mammut Sports Group Recalls Alugator Ride 3.0 Hoe and Alugator Ride SE Avalanche Shovels Due to Risk of Injury or Death
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mammut Sports Group Inc.
CPSC
Consumer productsReported Apr 6, 2023
Monti Kids Recalls Basket with Balls Toys Due to Choking Hazard (Recall Alert)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Monti Kids Inc.
CPSC
Reported Apr 5, 2023
Alcon Custom Pak Surgical Procedure Pack: Pak Number & Pak Description: 17533-04 DR GROSS LPS LLC 18704-03 CATARACT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research, LLC
FDA (openFDA device enforcement)
Reported Apr 5, 2023
Fentanyl 500mcg (2mcg/mL) and Ropivacaine HCl 250mg (1mg/mL) added to 250mL 0.9% Sodium Chloride, For Epidural Use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Apollo Care
FDA (openFDA drug enforcement)
Reported Apr 5, 2023
Dabigatran Etexilate Capsules, 75 mg, Rx Only, 60 Capsules per bottle, Manufactured by: Alkem Laboratories Ltd., INDIA,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ascend Laboratories, LLC
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Apr 5, 2023
Atrium Pneumostat Chest Drain Valve, Part Number 16100
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Atrium Medical Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 5, 2023
Automated Peritoneal Dialysis System. Used for automatic control of dialysis solution exchanges.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
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