Zimmer Biomet recalls non-cervical spinal fixation implants with reports of screws backing out post-surgery. Affected items have specific item numbers 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 non-cervical spinal fixation implants that may become loose after surgery. This could lead to improper spinal stabilization and potential complications.
The implants may not lock properly, causing the closure top to back out of the screw after surgery. This can lead to improper spinal stabilization and potential complications.
Patients who received the recalled Vital MIS Spinal Fixation implants for non-cervical spine procedures are most at risk. The recall applies to specific item numbers and lot numbers.
Check for item number 850M0055 on the implant packaging. The recall includes specific lot numbers: 136158, 136158, 143757, and 311626.
Reach out to Zimmer Biomet directly for details about your specific implant and next steps.
The specific item number is 850M0055.
The affected lot numbers are 136158, 136158, 143757, and 311626.
The recall does not specify an immediate stop; 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-2233-2020 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-2233-2020 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.
