Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 37–44 of 44 recalls
Retrospective; Their is the potential that implantable intramedullary lengthening nails may bend at the distal tail during insertion resulting in having to be replaced.
Potential for exoskeleton to lose lateral balance and cause patient to fall.
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Not all Electrocardiogram (ECG) events received July 2022-July 2024 were not properly routed and subsequently reviewed due to an analysis step being disabled with the monitoring service application software.