Zimmer Biomet, Inc. recalls Persona Partial Knee spacer block instruments; (1) 8mm block
See all recalls from Zimmer Biomet, Inc. →Recalled Product
Persona Partial Knee spacer block instruments; (1) 8mm block, Model Number: 42-5399-035-08; (2) 9mm block, Model Number:42-5399-035-09; (3) 10mm block, Model Number: 42-5399-035-10; (4) 12mm block, Model Number: 42-5399-035-12; (5) 14mm block, Model Number: 42-5399-035-14 A spacer block is used to ensure the tibial resection Is sufficient and to verify limb alignment. After verification the distal femoral resecUon Is complete using the distal femoral cut slot in the spacer block. The spacer block determines how much distal femoral bone is resected.
Hazard / Issue
Certain partial knee implant spacer blocks do not fit in the alignment tower instrument or handle.
Issued by
FDA
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for Persona Partial Knee spacer →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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