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Recall archive

94,408 stored notices, from Jun 20, 2012 to Sep 26, 2026.

31,892 recalls · page 173 of 1329

Medical devices

Reported Mar 12, 2025

AURORA Surgiscope System, Sterile, single use device that contains a Sheath, Obturator, and Imager. Manufacturer's…

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

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Food

Reported Mar 12, 2025

Pan de Coco (Coconut Rolls), net wt. 9oz (255g), product is packaged as 6 rolls on a yellow styrofoam plate, then…

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

Jesse's Bakery, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Mar 12, 2025

Garden Salad 12 oz Family Garden Salad 24 oz packed in clamshells

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

Jfe Franchising Inc.

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 12, 2025

CircuitGuard ThermoFlo Filter -Combined Heat and Moisture Exchanger, Bacterial Viral Filter w O2 Port and Elbow…

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

Kung Shin Plastics Co. Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 12, 2025

(1) Lumenis Pulse 120H 30 amp, REF GA 2009996, Laser System; (2) Lumenis Pulse 120H, Moses 2.0 (DOM), REF GA0006802,…

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

Lumenis, Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 12, 2025

Brand Name: TBS Osteo Product Name: TBS iNsight Model/Catalog Number: TBS iNsight v3.x / pn: OS-TBSi Software Version:…

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

Medimaps Group

FDA (openFDA device enforcement)

Medical devices

Reported Mar 12, 2025

Paradigm REF: MMT-712 and MMT-715

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

Medtronic MiniMed, Inc.

11 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 12, 2025

Medtronic Pipeline Vantage Embolization Device with Shield Technology, REF: PED3-027-350-12, PED3-027-350-14,…

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

Micro Therapeutics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 12, 2025

MIM software; System, Image Processing, Radiological

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

MIM Software Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 12, 2025

Vios Monitoring System Bedside Monitor Model BSM2050

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

Murata Vios, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 12, 2025

New Age International Inc. recalls Daily Veggies Enoki Mushroom due to Listeria monocytogenes

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

New Age International Inc.

FDA (recalls & safety alerts)

Food

Reported Mar 12, 2025

Item #96507 and item# 32901, King Harvest Balsamic Hummus, net wt. 10oz., UPC 025726 310097, perishable and…

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

Pacific Coast Fresh Co.

11 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 12, 2025

Philips IntelliSpace Cardiovascular software, Model 830089.

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

Philips Medical Systems Nederland B.V.

FDA (openFDA device enforcement)

Drugs

Reported Mar 12, 2025

Ergocalciferol - Vitamin D Supplement - 10 mcg (400 Units) per 0.05 mL Oral Syringe, Delivers: 0.05 mL Oral Solution,…

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

Safecor Health, LLC

4 more products in this recall

FDA (openFDA drug enforcement)

Food

Reported Mar 12, 2025

Noble Made Garlic Parmesan Wing Sauce, net wt 9.25oz, UPC 850000398542, #0897 BEST BY 06/02/2026 14:02 33724 L1, Code:…

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

Spicin Foods Inc.

FDA (openFDA food enforcement)

Drugs

Reported Mar 12, 2025

Morphine Sulfate Extended-Release Tablets, 100 mg, 100-count bottles, Rx Only, Manufactured by: Ohm Laboratories Inc.,…

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

Sun Pharmaceutical Industries Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Mar 12, 2025

TISSUE APPROXIMATION SYSTEM (TAS), Models T-4000, T-5000, T-LAP

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

TAS Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 12, 2025

Philips Connected Blood Glucose Meter, BGM 4; Model Number: TM0009;

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

Telcare, LLC

FDA (openFDA device enforcement)

Drugs

Reported Mar 12, 2025

Nelarabine Injection, 250mg/50mL, (5mg/mL), packaged in: a) 50 mL Single-Dose Vial, NDC 70710-1726-1; b) 6 x 50 mL…

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

Zydus Pharmaceuticals (USA) Inc.

1 more product in this recall

FDA (openFDA drug enforcement)

Food

Reported Mar 11, 2025

Liaoning Cheng Da USA Inc. recalls Wangzhihe Hot Pot Sauce due to Undeclared allergen - peanut, soy, sesame, and wheat

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

Liaoning Cheng Da USA Inc.

FDA (recalls & safety alerts)

Consumer products

Reported Mar 10, 2025

New York Wholesale Group recalls Zaarah Herbals Dietary Supplements due to Product may be contaminated with elevated levels of lead and arsenic

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

New York Wholesale Group

FDA (recalls & safety alerts)

Medical devices

Reported Mar 10, 2025

Smiths Medical recalls Portex Intubation Oral/Nasal Endotracheal Tubes due to Diameter of Device Smaller than Expected

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

Smiths Medical

FDA (recalls & safety alerts)

Consumer products

Reported Mar 6, 2025

Black Diamond Equipment Recalls BD Recon LT Avalanche Transceivers Due to Risk of Loss of Emergency Communications;…

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

Black Diamond Equipment Ltd.

CPSC

Consumer products

Reported Mar 6, 2025

Luv n' care Recalls Nuby Stroller Fans Due to Laceration Injury Hazard

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

Luv n' care

CPSC

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