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 spinal fixation implants that may back out after surgery. This could lead to complications if the implant fails to stay securely in place.
The extended tab screws in these implants may not lock securely, causing the implant to back out after surgery. This could lead to instability in the spine and potential complications.
Patients who received the specific spinal implant model (CANN POLY EXT TAB 7.5X50MM) with listed lot numbers are affected. Surgeons and medical staff who used these implants during procedures are at higher risk.
Check for the model number CANN POLY EXT TAB 7.5X50MM and lot numbers listed: C19I0004, C19J0002, C19J0022, C19L0009, C20B0003, SBM108416, SBM118998, SBM122215, SBM123980.
Identify the model number and lot numbers to confirm if your implant is affected.
Reach out to Zimmer Biomet for specific guidance on next steps and potential remedies.
The recalled model is CANN POLY EXT TAB 7.5X50MM with item number 810M7550.
Affected lot numbers include C19I0004, C19J0002, C19J0022, C19L0009, C20B0003, SBM108416, SBM118998, SBM122215, SBM123980.
Reports indicate that the extended tab screws may not lock securely, causing the implant to back out after surgery.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-2226-2020 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-2226-2020 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.
