🏥 Medical Devices • 15,809 recalls
Aspen Surgical Products
The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.
Aspen Surgical Products
The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.
LumiQuick Diagnostics
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
LumiQuick Diagnostics
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Aspen Surgical Products
The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.
Aspen Surgical Products
The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.
MedCare Products has determined that a number of their Floor Lifts manufactured from 9/1/2010 to 11/7/2012 do not meet MedCare's high standards. The original design includes a pin that over time and years of use may stop performing as designed and may break.
LumiQuick Diagnostics
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
LumiQuick Diagnostics
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Aspen Surgical Products
The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.
Remington Medical discovered an error on the FL-601-97 IFU; part number IFU-RM-0154. Specifically, the polarity for the black chuck in the picture is wrong. It shows (+), but should show (-).
Aspen Surgical Products
The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.
Aspen Surgical Products
The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.
Aspen Surgical Products
The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.
LumiQuick Diagnostics
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.
Central Purchasing LLC
Harbor Freight Tools intiaited a recall of Sit/Stand Rolling Walker (SKU/Item Number 66838, sold June 2009 to March 2014) because, over time, there is the possibility that a walker wheel may come off this product following repeated use without tightening the wheel bolt to the frame, presenting a potential hazard for the user.
The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.
Alcon LenSx received reports of unexpected downward motion of the gantry.
Aspen Surgical Products
The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.
LumiQuick Diagnostics
Products shipped to US locations that do not have approved applications for PMA , IDE or 510(k) clearance.