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Recall archive

94,908 stored notices, from Jun 20, 2012 to Oct 21, 2026.

32,164 recalls · page 463 of 1341

Medical devices

Reported Jan 26, 2022

ImagePilot Versions 1.92 and 1.93-software primarily facilitates processing and presentation of medical images on…

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

Konica Minolta Healthcare Americas, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Jan 26, 2022

SENNA Syrup (sennosides) 8.8 mg/ 5 mL unit-dose cups, packaged in 24 cups per carton, Mfg for: AvKARE, TN 38478, NDC…

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

Lohxa, LLC

FDA (openFDA drug enforcement)

Medical devices

Reported Jan 26, 2022

ARIES HSV 1&2 Assay, Part Number/REF 50-10017

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

Luminex Corporation

FDA (openFDA device enforcement)

Drugs

Reported Jan 26, 2022

Lexette (halobetasol propionate) Topical Foam, 0.05% 50 g canisters, Rx ONLY, Distributed by: Mayne Pharma Greenville,…

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

Mayne Pharma Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Jan 26, 2022

Physicians CARE Extra Strength PAIN RELIEVER [Acetaminophen, Aspirin (NSAID), and Caffeine], 250 mg, 250 mg, 65 mg,…

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

Medique Products

2 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Jan 26, 2022

KWIK-STIK 2 Pack, Catalog #0894P; KWIK-STIK 6 Pack, Catalog #0894K; and LYFO DISK, Catalog #0894L; Microsporum canis…

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

Microbiologics Inc.

FDA (openFDA device enforcement)

Consumer products

Reported Jan 26, 2022

Family Dollar Recalls Beach Loungers Due to Injury Hazard

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

Midwood Brands LLC, an affiliate of Family Dollar

CPSC

Drugs

Reported Jan 26, 2022

Semglee (insulin glargine) injection, 100 units/mL (U-100), 3 mL Prefilled Pen (NDC 49502-0196-71), packaged in Five 3…

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

Mylan Pharmaceuticals Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Jan 26, 2022

VITROS Immunodiagnostic Products High Sample Diluent A Reagent Pack

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 26, 2022

Infa-Therm Transport Mattress, Reference Number 989805616831 1015

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

Philips North America LLC

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 26, 2022

ZOCALO AJI LIMO DRIED CHILI PODS- ORGANIC, Dried Aji Peppers for consumer consumption. Product is vacuum sealed in…

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

Power Selles Imports dba Culinary Collective

FDA (openFDA food enforcement)

Medical devices

Reported Jan 26, 2022

1. Sensis, material # 10764561; UDI: 04056869010137 2. Sensis Vibe Hemo, material # 11007641; UDI: 04056869010199 3.…

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 26, 2022

Senior Living Arial Emergency and Nurse Call Systems

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

Stanley Security Solutions Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 26, 2022

Neodent Easypack Helix GM Acqua 3.5X8/Smart 4.5X2.5 -intended for dental implant Item 138.089

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

Straumann USA LLC

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Jan 26, 2022

Brinzolamide Ophthalmic Suspension, USP 1%, packaged as a)10 ml dropper bottles (NDC 0591-2127-79), and b) 15 ml…

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

Teva Pharmaceuticals USA

FDA (openFDA drug enforcement)

Drugs

Reported Jan 26, 2022

Clobazam Oral Suspension 2.5 mg/mL, 120 mL bottles, Rx only, Manufactured by: VistaPharm, Inc. Largo, FL 33771, NDC…

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

VistaPharm, Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Jan 19, 2022

Morphine Sulfate Oral Solution 100 mg per 5 mL (20 mg/mL) 30 mL bottles, Rx only, Hi-Tech Pharmacal Co., Inc.,…

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

Akorn, Inc.

2 more products in this recall

FDA (openFDA drug enforcement)

Food

Reported Jan 19, 2022

8 Grain Bread, Bosket Bread brand. The Net weight of the products range from 1-1.5 lbs. No UPC. Product is packaged in…

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

Bosket Bread Company, LLC

14 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 19, 2022

Flat Panel Detector, Model Number: TFP-800A, used with the Alphenix Systems, Item Numbers: INFX-8000V, INFX-8000C,…

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

Canon Medical System, USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 19, 2022

LigaSure Blunt Tip Laparoscopic Sealer/Divider, Nano-Coated, Product Number LF1837

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

Covidien LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jan 19, 2022

GLOBAL UNITE STD STEM SZ 6 Part Number: 11000610

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

DePuy Orthopaedics, Inc.

7 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 19, 2022

100% Plant-Based Dream Pops Vanilla Sky Bites UPC 854097008254

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

Dream Pops

3 more products in this recall

FDA (openFDA food enforcement)

Drugs

Reported Jan 19, 2022

8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL), 50 mL vials, Rx Only, Manufactured and Distributed by:…

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

Exela Pharma Sciences LLC

FDA (openFDA drug enforcement)

Consumer products

Reported Jan 19, 2022

Mushie & Co Recalls FRIGG Silicone Pacifiers Due to Choking Hazard

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

FRIGG Production ApS / FB Trading ApS

CPSC

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