Skip to main content

Recalls from Howmedica Osteonics Corp.

Recalls from Howmedica Osteonics Corp. filed with the FDA, USDA FSIS, CPSC or NHTSA, newest first. Company page 4 recalls Each recall is dated by the day its recall page names (how recalls are dated).
Filters · 1Sort Newest
Agency
Risk level
Status
Date
Sold in

1 recall that day

Howmedica Osteonics Triathlon Hinge Femoral Prep, Femoral Prep, Misc. Instruments and Universal Baseplate Finishing Trays

The reprocessing instructions specify a 30-minute dry time for trays sterilized in blue wrap.

Moderate risk, FDA, Device defect

1 recall that day

Howmedica Osteonics Orthopaedic Implant Components

Orthopaedic implant components made with aged polyethylene may wear excessively.

Moderate risk, FDA, Device defect

1 recall that day

Howmedica Osteonics Tri TS Baseplate

Triathlon Universal Baseplate Size 3 and Size 4 are in packaging labeled with the other size.

Moderate risk, FDA, Labeling error

1 recall that day

Howmedica Osteonics MICS3 Angled Sagittal Saw Attachment

The MICS3 Angled Sagittal Saw Attachment has screws that may loosen and detach during use.

Moderate risk, FDA, Device defect