Zimmer Biomet recalls certain spinal fixation implants due to reports of screws backing out post-surgery. Affected items have specific model numbers and lot codes. 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 specific spinal implants that may loosen after surgery. This could lead to the device failing to stay securely in place, potentially causing complications.
The implants have a reported issue where the extended tab screws can become loose after surgery. This may cause the device to back out of the screw post-operatively, potentially leading to instability in the spinal area.
Patients who received the recalled spinal implants during surgery are most at risk. The recall affects individuals who used the specific model numbers listed in the notice.
Check for the model number CANN POLY EXT TAB 4.5X35MM and item number 810M4535. The recall includes specific lot numbers: C20B0010, SBM108400, SBM118982, SBM121611.
Reach out to Zimmer Biomet directly for information about your specific implant and next steps.
There are reports of inadequate locking of the extended tab screws, which can cause the closure top to back out of the screw post-operatively.
The affected model is CANN POLY EXT TAB 4.5X35MM with item number 810M4535 and specific lot numbers: C20B0010, SBM108400, SBM118982, SBM121611.
The recall does not require immediate removal; however, affected patients should contact Zimmer Biomet for guidance.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-2211-2020 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-2211-2020 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.
