Recall archive
31,892 recalls · page 211 of 1329
Reported Oct 18, 2024
Church Brothers, LLC recalls Multiple brand names Green Onions due to Salmonella
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Church Brothers, LLC
FDA (recalls & safety alerts)
Reported Oct 18, 2024
Dakota Tom’s Sandwiches recalls Dakota Tom’s Pepperjack Cheeseburger, Bacon Cheeseburger and The Gambler due to Potential Foodborne Illness - Listeria…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Dakota Tom’s Sandwiches
FDA (recalls & safety alerts)
Reported Oct 18, 2024
Medtronic plc recalls Medtronic MiniMed™ 600 series or 700 series insulin pumps due to Device & Drug Safety - Defect
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Medtronic PLC
FDA (recalls & safety alerts)
Consumer productsReported Oct 17, 2024
Anker Power Banks Recalled Due to Fire and Burn Hazards; Manufactured by Anker Innovations
High riskUsing this product could cause serious injury, illness or death — stop using it now.Anker Innovations Limited
CPSC
Consumer productsReported Oct 17, 2024
Colsen Recalls Fire Pits Due to Risk of Serious Burn Injury from Flame Jetting and Fire Spreading Hazards
High riskUsing this product could cause serious injury, illness or death — stop using it now.Colsen Fire Pits LLC
CPSC
Consumer productsReported Oct 17, 2024
Textron Specialized Vehicles Expands Recall of Arctic Cat and Tracker Side by Side Recreational Off Highway Vehicles…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Textron Specialized Vehicles
CPSC
Consumer productsReported Oct 17, 2024
Oliva Cigars Recalls Cigar Slim Lighters Due to Missing Child Safety Feature, Posing Burn and Fire Hazards; Violations…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wenzhou LingShuo Smoking Accessories Co. Ltd.
CPSC
Reported Oct 16, 2024
Vail-Bon Jie Yang Wan capsules, 30-count bottle, Vall Boon Medical Factory Sdn. Bhd., No 1, Lorong Mengkudu, Taman…
High riskUsing this product could cause serious injury, illness or death — stop using it now.123Herbals
FDA (openFDA drug enforcement)
Reported Oct 16, 2024
3M Tegaderm CHG, Chlorhexidine Gluconate I.V. Securement Dressing, REF 1658R
Moderate riskThis product could cause temporary or reversible health problems — stop using it.3M Company - Health Care Business
FDA (openFDA device enforcement)
Reported Oct 16, 2024
Enterprise Imaging XERO Viewer- software application used for reference and diagnostic viewing of multispecialty…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Agfa Healthcare NV
FDA (openFDA device enforcement)
Reported Oct 16, 2024
Gelato ice cream packaged in Compostable Tubs which are labeled in part Vaschetta Accoppiata Compostabile . The gelato…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Alcas USA Corp.
FDA (openFDA food enforcement)
Reported Oct 16, 2024
iCast Covered Stent, 6MMx16MMx120CM, Model Number 42616
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Atrium Medical Corporation
FDA (openFDA device enforcement)
Reported Oct 16, 2024
Monarch Platform (Endoscopy), REF: MON-000005-01, MON-000005-01R. Monarch Platform (Bronchoscopy), REF: MON-000006,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Auris Health Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 16, 2024
Beckman Coulter Dxl 9000 Access Immunoassay Analyzer, REF #C11137. An in vitro diagnostic device used for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
FDA (openFDA device enforcement)
Reported Oct 16, 2024
BD Synapsys Informatics Solution with software versions: 4.20, 4.30, 5.10, 5.20 and 5.30- IVD standalone laboratory…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Oct 16, 2024
C&A Naturistics recalls AK Forte AK Forte Dietary Supplement due to Device & Drug Safety – Unapproved Drug
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.C&A Naturistics
FDA (recalls & safety alerts)
Reported Oct 16, 2024
Minute Maid Zero Sugar Lemonade 12 cans carton UPC 0 25000 12115 9 CANNED UNDER THE AUTHORITY OF THE COCA-COLA COMPANY,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.COCA COLA Consolidated LLC
FDA (openFDA food enforcement)
Reported Oct 16, 2024
Check-Flo Performer Introducer Set, Reference Part Number RCF-5.0-35-45-J, Order Number G27242. Performer Introducers…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Incorporated
FDA (openFDA device enforcement)
Reported Oct 16, 2024
GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model/Catalog/Code Numbers: a)¿¿¿¿¿ 2089507-120;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
FDA (openFDA device enforcement)
Reported Oct 16, 2024
Triathlon Universal TS Baseplate Size 2 - A single use sterile implantable device intended for cemented applications…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 16, 2024
7-Eleven Fudge Brownie with Chocolate Chip, 3.5 oz. UPC: 05254856392
High riskUsing this product could cause serious injury, illness or death — stop using it now.Innovation Bakers, LLC
FDA (openFDA food enforcement)
Reported Oct 16, 2024
Inspire Model 4340 Respiratory Sensing Lead, component of the Inspire Upper Airway Stimulation (UAS) system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Inspire Medical Systems Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 16, 2024
MEDIHONEY Dressing with Active Leptospermum Honey Wound and Burn Dressing W/APPLICATOR, 1.5oz tube (Model Number 31515)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Oct 16, 2024
NxTAG Respiratory Pathogen Panel, REF: I051C0447
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Molecular Diagnostics Inc.
1 more product in this recall
FDA (openFDA device enforcement)
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