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Recall archive

94,526 stored notices, from Jun 20, 2012 to Oct 2, 2026.

31,892 recalls · page 326 of 1329

Consumer products

Reported Aug 3, 2023

American Honda Recalls Portable Generators Due to Fire Hazard

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

American Honda Motor Co. Inc.

CPSC

Consumer products

Reported Aug 3, 2023

Daikin Comfort Technologies Recalls Amana Packaged Terminal Air Conditioners and Heat Pumps Due to Burn and Fire…

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

Daikin Comfort Technologies Manufacturing LP (DCT)

CPSC

Consumer products

Reported Aug 3, 2023

Crate & Barrel Recalls Table Lamps Due to Fire Hazard (Recall Alert)

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

Euromarket Designs Inc., d/b/a Crate & Barrel

CPSC

Consumer products

Reported Aug 3, 2023

Maggie's Farm Recalls Aerosol Bed Bug & Flea Killer Cans Due to Injury and Laceration Hazards

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

Maggie's Farm Ltd.

CPSC

Consumer products

Reported Aug 3, 2023

Philips Avent Digital Video Baby Monitors Recalled by Philips Personal Health Due to Burn Hazard

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

Philips Consumer Lifestyle B.V.

CPSC

Drugs

Reported Aug 2, 2023

Diclofenac Sodium Topical Solution USP, 2% w/w, 3.8 FL.OZ.(112 grams) bottles, Rx only, Manufactured for: Alembic…

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

Alembic Pharmaceuticals, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Aug 2, 2023

Argon Medical Devices, REF 352506070E, Option Elite Retrievable Vena Cava Filter, Suitable of Jugular or Femoral…

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

Argon Medical Devices, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 2, 2023

Ringed DxI Reaction Vessels (RVs)

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

Beckman Coulter, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 2, 2023

Flexiva Pulse 242 Single-Use Laser Fibers-intended to be used as a device that transmits Ho:YAG laser energy from…

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

Boston Scientific Corporation

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 2, 2023

YAMATO PLUS IAB; intra-aortic balloon catheter and accessories used to provide counter pulsation therapy in the aorta.…

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

Datascope Corp.

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 2, 2023

Ventralight ST 4" x 6" Ellipse with Echo PS Catalog Number: 5955460

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

Davol, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 2, 2023

Natural Systems, Naturasys MULTI VITAMIN HIGH POTENCY AND FORMULATION, Dietary Supplement 60 Tablets

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

Emceta International Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 2, 2023

HAMILTON C1 Ventilator REF 161001 1610010 Is intended to provide positive pressure ventilatory support to adults and…

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

Hamilton Medical, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 2, 2023

Zinc Sulfate Monohydrate, USP, Powder. Net Wt: 55 lb / 25 kg. Jost Chemical 8150 Lackland, St. Louis, MO 63114.…

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

Jost Chemical Co.

FDA (openFDA food enforcement)

Drugs

Reported Aug 2, 2023

Safe Tussin DM Cough + Chest Congestion (Dextromethorphan HBr/ Cough Suppressant Guaifenesin/Expectorant), packaged in…

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

Kramer Laboratories, Inc.

1 more product in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Aug 2, 2023

DYND3000xxP Series - Flexible Laryngeal Mask Airway Packs

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

MEDLINE INDUSTRIES, LP - Northfield

FDA (openFDA device enforcement)

Medical devices

Reported Aug 2, 2023

A901 Communication Manager Application, used in conjunction with the A710 Clinician Programmer application..

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

Medtronic Neuromodulation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 2, 2023

FRED Flow Re-Direction Endoluminal Device, REF: FRED3507-PMA, FRED3511, FRED3511-PMA, FRED3516-CA, FRED3516-PMA,…

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

Microvention Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 2, 2023

SPRING VALLEY brand POTATO BLINTZES; NET WT. 13 OZ (369g); KEEP FROZEN; READY TO COOK; INGREDIENTS: WHEAT FLOUR (WHET…

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

Milmar Food Corp.

FDA (openFDA food enforcement)

Drugs

Reported Aug 2, 2023

Testosterone Cypionate-Testosterone Propionate 180-20 mg/mL in cottonseed oil, Compounded Rx, For Intramuscular Use…

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

New Vitalis Pharmacy LLC dba New Vitalis Pharmacy

FDA (openFDA drug enforcement)

Medical devices

Reported Aug 2, 2023

VITROS Immunodiagnostic Products NT-proBNP II Range Verifiers-For in vitro diagnostic use only. For use in verifying…

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

Ortho-Clinical Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 2, 2023

QIAstat-Dx¿ Respiratory SARS-CoV-2 Panel -IVD intended for the detection and differentiation of nucleic acid from…

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

Qiagen GmbH

2 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Aug 2, 2023

Oxacillin for Injection, USP, 1 gram per vial, For IV or IM Use, Rx only, Mfd. for SAGENT Pharmaceuticals, Schaumburg,…

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

Sagent Pharmaceuticals

2 more products in this recall

FDA (openFDA drug enforcement)

Drugs

Reported Aug 2, 2023

FentaNYL 500 mcg/250 mL - Bupivacaine HCl 0.1% in 0.9% Sodium Chloride 250mL Bag, Injection for Epidural Use (fentaNYL…

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

SCA Pharmaceuticals

FDA (openFDA drug enforcement)

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