Zimmer Biomet recalls certain spinal fixation implants due to reports of screws backing out post-surgery. Affected items have specific model and lot numbers. 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 fixation implants that may loosen after surgery. This could lead to complications if the screws become unstable.
The screws may not lock properly after surgery, causing the implant to become loose. This could lead to instability in the spine and potential complications.
Patients who received the recalled implants during surgery are most at risk. The recall applies to specific model numbers and lot numbers used in spinal procedures.
Check for the model number CANN BL POLY EXT 8.5X5:55MM and lot numbers SBM109985 or SBM109986. The product is used in spinal surgeries for posterior pedicle screw fixation.
Reach out to Zimmer Biomet directly for specific guidance on the recalled implants.
The model number is CANN BL POLY EXT 8.5X55MM with item number 811M8555.
Lot numbers SBM109985 and SBM109986 are affected.
There are reports that the screws may not lock properly after surgery, causing the implant to become loose.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-2231-2020 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-2231-2020 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.
