Due to product design and process control, part of the device can separate and remain behind when the device is removed that can potentially cause permanent impairment or damage to body function or structure.
Surgical Instruments
🏥 Medical Devices • 7,015 recalls
Synthes Flexible Shaft, Orthopedic manual surgical instrument The Flexible shafts are intended for use as an optional reaming step in intramedullary nailing systems.
Synthes (USA) Products
Non-conforming material used.
DePuy Orthopaedics, Inc. is issuing a voluntary recall for all lots of the ACTIS Flex Reamers due to the instruments breaking and potentially leaving pieces in the patient.
Inpeco received several notifications from the field about burnt schuko sockets. The customers reported that some smoke was seen coming from the damaged sockets.
Screws were identified as having the incorrect part number and lot number marked upon them. The part number incorrectly indicated a length of 115 mm rather than 110 mm. The lot number incorrectly indicated lot number of TSL003765 rather than TSL003721.
Trocar Catheters are packaged with a label containing an icon that shows more holes (eyelets) than the product actually contains.
Alphatec Spine is recalling the Arsenal Spinal Fixation System Set Screw due to a trend in set screw postoperative disengagement from the screw body.
Trocar Catheters are packaged with a label containing an icon that shows more holes (eyelets) than the product actually contains.
Trocar Catheters are packaged with a label containing an icon that shows more holes (eyelets) than the product actually contains.
Trocar Catheters are packaged with a label containing an icon that shows more holes (eyelets) than the product actually contains.
Misbranding; the product labeled as an Antibacterial Hydrophilic Intermittent Catheter, is instead an Antibacterial Intermittent Catheter (no Hydrophilic Coating).
Trocar Catheters are packaged with a label containing an icon that shows more holes (eyelets) than the product actually contains.
Trocar Catheters are packaged with a label containing an icon that shows more holes (eyelets) than the product actually contains.
Trocar Catheters are packaged with a label containing an icon that shows more holes (eyelets) than the product actually contains.
Trocar Catheters are packaged with a label containing an icon that shows more holes (eyelets) than the product actually contains.
Added Instructions for Use: After application, inspect the Light Glove for barrier integrity
Accessory Adapter Part number 600525A0 Product Usage: designed for the mounting of MAQUET accessories with the dovetail guide interface immediately before, during and after surgical interventions as well as for examination and treatment.
Maquet Medical Systems USA
Maquet Inc. is initiating a voluntary field action on the Accessory Adapter part number 600525A0 due to a complaint in which a head rest mounted to the accessory adapter slipped out of the mountain rail.
Contract manufacturer packaged an incorrect sheath with the product. Packaged 30Fr instead of 24Fr.
Mislabeled product: Sterilization pouch and carton labeled as Standard Type instead of Short type
Mislabeled product: Sterilization pouch and carton box labeled as Standard type instead of Jr type-Long