Recall archive
31,892 recalls · page 219 of 1329
Reported Sep 18, 2024
25-LHP-828, HeNe Laser System, 35 mW
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pacific Lasertech, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 18, 2024
BARRIER THERAPY SKIN PROTECTANT CREAM (1% colloidal oatmeal), 10 FL OZ/296 ML- tube, Distributed By: Prequel, LOS…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Prequel Skin
FDA (openFDA drug enforcement)
Reported Sep 18, 2024
UPC 71117 19063, Reser's American Classics Garden Pasta Salad 16oz, refrigerated, packaged in an opaque printed plastic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Reser's Fine Foods, Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 18, 2024
Asli Cinnamon Powder, 7oz clear plastic pouch, UPC 703440150723
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sands Impex Inc. dba Asli Fine Foods
FDA (openFDA food enforcement)
Reported Sep 18, 2024
Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP); Siemens Material Number (SMN): 11097543
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 18, 2024
ROTATION MEDICAL TENDON STAPLES (8) (broad indication)-Intended for fixation of prosthetic material to soft tissues.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 18, 2024
Pneupac paraPAC plus 300 ventilator kit, REF P300NXX
High riskUsing this product could cause serious injury, illness or death — stop using it now.Smiths Medical ASD Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 18, 2024
Syringes with Fixed Needles labeled as: a) SOL-M: 1) SOL-M 1ml TB Syringe w/Fixed Needle 25G*5/8'', Model No. 181025,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sol-Millennium Medical Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 18, 2024
NEUROSIGN Disposable Stimulating Dissector, REF 5888-00
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Technomed Europe
FDA (openFDA device enforcement)
Reported Sep 18, 2024
Brand Name: Vit-l-escence Product Name: Vit-l-escence Singles A3 Model/Catalog Number: 1203- Software Version: N/A…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ultradent Products, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 18, 2024
Biolox Option Taper Sleeve, Type 1 Taper, Standard Neck - Indicated for use in total hip replacement with cemented or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer GmbH
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 18, 2024
Spacelabs Ultraview DM3 Vital Signs Monitor (all variations -M, -MT, -N, -NT), Model Number 91330
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zoe Medical Incorporated
1 more product in this recall
FDA (openFDA device enforcement)
Consumer productsReported Sep 12, 2024
About 866,000 AirJet and HydroJet Spa Pumps Recalled Due to Fire Hazard; One Death Reported; Manufactured by Bestway…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bestway (Hong Kong) International Ltd.
CPSC
Consumer productsReported Sep 12, 2024
Red Toolbox Recalls Stanley-Branded Jr. Kids Garden Sets Due to Lead Poisoning Hazard; Violation of Federal Ban for…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Costco Wholesale
CPSC
Reported Sep 12, 2024
Dearborn Sausage Company, Inc. Recalls Wiener Products Due to Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dearborn Sausage Company Inc.
USDA FSIS
Consumer productsReported Sep 12, 2024
Glen Dimplex Americas Recalls Cadet Apex72 Electric Heaters Due to Fire Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Glen Dimplex Americas Ltd.
CPSC
Consumer productsReported Sep 12, 2024
GOETAS Pool Drain Covers Recalled Due to Entrapment Hazard; Violation of the Virginia Graeme Baker Pool and Spa Safety…
High riskUsing this product could cause serious injury, illness or death — stop using it now.GuangZhouShiYiYangKangTiSheBeiYouXianGongSi, dba GOETAS
CPSC
Consumer productsReported Sep 12, 2024
Intellio Toys Recalls Bright Builder Fort Kits Due to Battery Ingestion Hazard; Violation of Federal Regulations for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Intellio Toys
CPSC
Consumer productsReported Sep 12, 2024
Petzl America Recalls GYM, PANDION and PANJI Climbing Harnesses Due to Fall Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Petzl America, Inc.
CPSC
Consumer productsReported Sep 12, 2024
MJKSARE High Chairs Recalled Due to Entrapment and Fall Hazards; Violation of Federal Regulation for High Chairs;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Worldwide Windows Inc.
CPSC
Reported Sep 11, 2024
Impella CP Smart Assist Set, EU; Product Code: 0048-0014;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abiomed, Inc.
17 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 11, 2024
Heparin (Heparin Sodium in 0.9% Sodium Chloride Injection), 2,000 units per 1,000 mL (2 units/mL), 1000 mL Sterile…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Baxter Healthcare Corporation
FDA (openFDA drug enforcement)
Reported Sep 11, 2024
Power Express, REF B90918
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Biomedical GmbH
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 11, 2024
DxI 9000 Access Immunoassay Analyzer, REF C11137, vitro diagnostic device used for the quantitative, semi-quantitative,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
FDA (openFDA device enforcement)
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