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Recall archive

94,391 stored notices, from Jun 20, 2012 to Sep 23, 2026.

31,892 recalls · page 120 of 1329

Medical devices

Reported Sep 17, 2025

Reef TA Inserter, Part Number: TA2-001003, part of the Reef Interbody System

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

Seaspine Orthopedics Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Sep 17, 2025

Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP). Material Number: 11097543.

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 17, 2025

Artis Pheno. Image-Intensified Flouroscopic X-Ray System.

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Sep 17, 2025

Sulfamethoxazole and Trimethoprim, USP, 800 mg/160 mg, Double Strength, 100 Tablets unit dose blister packs (10x10) per…

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

The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

1 more product in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Sep 17, 2025

LinkSymphoKnee System, Tibial Component, Modular, Symmetric, Sz. 5, CoCrMo/TiNbN, cemented, Fixed. REF Number:…

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

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA (openFDA device enforcement)

Medical devices

Reported Sep 17, 2025

Wasatch Photonics 785/830-SR and 785-ER-ILC Raman Spectrometers, Product Models: 785-SR-ILP, 785-SR-ILC, 830-SR-ILP,…

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

Wasatch Photonics

FDA (openFDA device enforcement)

Food

Reported Sep 17, 2025

Wegmans Medium Camembert Soft Ripened Cheese - 8.8oz - Round wooded container; UPC: 2-77467-00000-7 , 0-77890-53515-8

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

Wegmans Food Markets, Inc.

3 more products in this recall

FDA (openFDA food enforcement)

Drugs

Reported Sep 17, 2025

Iodo Blanco Iodides, First Aid Antiseptic, Mercury Free, Iodine 2%, First Aid Antiseptic, Contains 1 fl. oz (30 ml) per…

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

World Perfumes Inc.

FDA (openFDA drug enforcement)

Drugs

Reported Sep 17, 2025

Succinylcholine Chloride Injection, USP 200 mg/10 mL (20 mg/mL), Rx only, 10 mL Multiple-dose Vial, Sterile,…

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

Zydus Pharmaceuticals (USA) Inc.

10 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Sep 15, 2025

BD recalls BD Alaris BD Alaris Pump Module model 8100 used with a subset of compatible pump infusion sets due to Pump performance variations compared to the…

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

Bd

FDA (recalls & safety alerts)

Meat & poultry

Reported Sep 15, 2025

Quality Poultry & Seafood, Inc. Recalls Various Catfish Fillet Products Produced Without Benefit of Inspection

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

Quality Seafood & Poultry, Inc.

USDA FSIS

Consumer products

Reported Sep 11, 2025

Epoca International Recalls Paris Hilton Mini Beauty Fridges Due to Fire and Burn Hazards

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

Epoca International LLC

CPSC

Food

Reported Sep 11, 2025

Gooder Foods, Inc recalls Goodles Flavored pasta due to Undeclared milk and cashews

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

Gooder Foods, Inc.

FDA (recalls & safety alerts)

Consumer products

Reported Sep 11, 2025

In My Jammers Recalls Button Flare Pajama Sets Due to Burn Hazard; Violates Mandatory Flammability Standards

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

In My Jammers

CPSC

Consumer products

Reported Sep 11, 2025

Blueroot Health Recalls Bottles of Bariatric Fusion Iron Multivitamins Due to Risk of Serious Injury or Death from…

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

VitaQuest International, LLC

CPSC

Consumer products

Reported Sep 11, 2025

Shierdu Children's Toys Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violates the Small Parts…

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

Yiwu Shiyi Trading Co., Ltd.

CPSC

Drugs

Reported Sep 10, 2025

Sulfamethoxazole and Trimethoprim Tablets, USP 800mg/160mg, Double Strength, Rx Only, Packaged as a) 100-count bottle,…

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

Amneal Pharmaceuticals, LLC

4 more products in this recall

FDA (openFDA drug enforcement)

Drugs

Reported Sep 10, 2025

Lactated Ringers's Injection USP, 1000 mL container, Rx only, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC…

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

B Braun Medical Inc.

1 more product in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Sep 10, 2025

Novum IQ LVP (Large Volume Pump), Product Code 40700BAXUS, infusion pump

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

Baxter Healthcare Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Sep 10, 2025

FSIS Issues Public Health Alert for Raw Sirloin Beef Tip Product Due to Misbranding and Undeclared Allergens

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

Bianco Inc.

USDA FSIS

Medical devices

Reported Sep 10, 2025

Platelia Toxo IgM Catalog Number 26211 UDI Code: 03610520005552 The Platelia Toxo IgM assay is a semi-quantitative…

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

Bio-Rad Laboratories, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Sep 10, 2025

Semaglutide, 2.5 mg/mL injection, 2 mL., Boothwyn Pharmacy

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

Boothwyn Pharmacy LLC

3 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Sep 10, 2025

WATCHMAN TruSeal Access System SGL, OUS, Material Number (UPN) M635TS70010; intended to provide vascular and…

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

Boston Scientific Corporation

10 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 10, 2025

Superion IDS Kit Superion Indirect Decompression System 8MM, VF Implant 101-9808 00884662000529 Superion Indirect…

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

Boston Scientific Neuromodulation Corporation

FDA (openFDA device enforcement)

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