Zimmer Biomet recalls spinal fixation implants with inadequate screw locking that may back out post-surgery. Affected items include specific model numbers and lot ranges. Consumers should contact the company for details.
There are reports of inadequate locking of the extended tab screws. Complaints were reported where the closure top backed out of the screw post-operatively.
Zimmer Biomet is recalling spinal fixation implants that may back out after surgery due to poor screw locking. This could lead to complications for patients who have had spinal surgery. The recall affects specific model numbers and production lots.
The extended tab screws in these implants may not lock properly, causing the closure top to back out after surgery. This can lead to instability in the spinal fixation site and potential complications.
Patients who received the recalled spinal implants during surgery are most at risk. The recall applies to specific model numbers and production lots used in non-cervical spinal fixation procedures.
Check for the model number CANN POLY EXT TAB 5.5X50MM and item number 810M5550. Affected items were produced with specific lot numbers including C19H0010 through SBM122122.
Reach out to Zimmer Biomet for specific guidance on whether your implant is affected and next steps.
The recalled model is CANN POLY EXT TAB 5.5X50MM with item number 810M5550.
Patients who received the recalled spinal implants during surgery are most at risk.
Check for the model number CANN POLY EXT TAB 5.5X50MM and item number 810M5550, and verify your lot number against the listed production lots.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-2217-2020 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-2217-2020 from Zimmer Biomet. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
