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Recall archive

94,519 stored notices, from Jun 20, 2012 to Sep 28, 2026.

31,892 recalls · page 282 of 1329

Medical devices

Reported Jan 31, 2024

Bard Nasogastric Sump Tube with ENFit, 10Fr., 36in Long, REF EN0042100

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

C.R. Bard Inc.

16 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 31, 2024

DeIorio Foods, Inc. brand Cafe Pizza Dough Sheet; Keep Frozen

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

DeIorio Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 31, 2024

DiaSorin LIAISON HSV-2 Type Specific IgG, REF 310620

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Diasorin Inc.

FDA (openFDA device enforcement)

Drugs

Reported Jan 31, 2024

Fluocinolone Acetonide Oil, 0.01% (Ear Drops), package in 1 Oz. (20 mL fill volume) bottle, Rx only, Manufactured by:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Glenmark Pharmaceuticals Inc., USA

FDA (openFDA drug enforcement)

Drugs

Reported Jan 31, 2024

Robitussin Honey CF Max Non-Drowsy Adult (Acetaminophen 650mg, Dextromethorphan HBr 20 mg), a) 4 FL OZ (118mL) and b) 8…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Haleon US Holdings LLC

1 more product in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Jan 31, 2024

PANTHER FUSION System REF 9121010000 The Panther System is an integrated nucleic acid testing system which fully…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hologic, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Jan 31, 2024

Vasopressin 2 Unit/2 mL in 0.9% Sodium Chloride, 2 mL per syringe, Rx Only, 719 Kasota Ave SE, Minneapolis, MN. NDC…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

IntegraDose Compounding Services LLC

FDA (openFDA drug enforcement)

Medical devices

Reported Jan 31, 2024

Snapshot NIR, REF: KD204

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Kent Imaging, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 31, 2024

Pan de Racho (Feria), Net Wt. 2lbs, individually packaged in clear plastic bag.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Lara's Bakery 3 LLC

4 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jan 31, 2024

R&B Chocolate Chips Croissant Twist

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Lecoq Cuisine Corporation

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Jan 31, 2024

Duc De Coeur Camembert Cheese Croquettes Frozen NET WT 9 OZ (256g) UPC 2023 8391 Packaged in a cardboard cartons.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Lidl US TRADING

FDA (openFDA food enforcement)

Medical devices

Reported Jan 31, 2024

Cobalt XT DR MRI SureScan Implantable Cardioverter Defibrillator, product number DDPA2D1

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 31, 2024

Model A710 Intellis Clinician Programmer Application, version 2.0.97

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Neuromodulation

FDA (openFDA device enforcement)

Medical devices

Reported Jan 31, 2024

VITROS Immunodiagnostic Products Anti-HBs Quantitative Reagent Pack, Catalog No. 6801925 VITROS Immunodiagnostic…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ortho-Clinical Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 31, 2024

Power Knee, REF: PKA10001, and PKA10003; with Power Knee Battery, REF: PKA10002

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ossur H / F

FDA (openFDA device enforcement)

Drugs

Reported Jan 31, 2024

Bleomycin for Injection, USP, 15 units per vial, 1 single dose glass fliptop vial, Rx Only, Distributed by: Hospira,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Pfizer

FDA (openFDA drug enforcement)

Medical devices

Reported Jan 31, 2024

EliA GBM Wells, Material Number 14551401, for Phadia 250, 2500, and 5000. In vitro diagnostic

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Phadia Ab

FDA (openFDA device enforcement)

Medical devices

Reported Jan 31, 2024

Achieva 1.5T, Model No. 781178, 781196, 781296

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Philips North America

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 31, 2024

Publix Custom Made Sub Sandwiches, variable weights and sizes, individually wrapped in paper, intended for immediate…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Publix Super Markets, Inc.

5 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jan 31, 2024

365 Whole Foods Vegan Ultimate Veggie, Thin Cust Pizza. Item # 999209512 Topped with Vegan Mozzarella-Style Cheese,…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Richelieu Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 31, 2024

Sedecal X Optima URS digital mobile diagnostic x-ray system. A a stationary x-ray unit with a universal swivel arm. It…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Sedecal Sa

FDA (openFDA device enforcement)

Medical devices

Reported Jan 31, 2024

TactiFlex Ablation Sensor Enabled Ablation Catheter, Models A-TFSE-FJ, 7.5 F shaft and an 8F distal section, Sterile.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

St. Jude Medical, Atrial Fibrillation Division, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 31, 2024

Vermont Village Unsweetened Apple Sauce (24oz)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stonewall Kitchen, LLC

FDA (openFDA food enforcement)

Drugs

Reported Jan 31, 2024

Methoxsalen Capsules, USP 10mg, 50-count bottle, Rx Only, Manufactured by: Strides Pharma Science Ltd. Bengaluru -…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Strides Pharma Inc.

FDA (openFDA drug enforcement)

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