Zimmer Biomet recalls certain soft tissue implants due to improper assembly causing shaft shift and potential device breakage. Affected items include specific model numbers and lot numbers listed in the recall notice.
It was identified that the product was not assembled correctly causing the implant shaft to shift and fall out during the opening of the device, which potentially could break the device.
Zimmer Biomet is recalling specific soft tissue implants that may shift or break during use due to improper assembly. This could lead to the device becoming ineffective or causing injury if not addressed.
The implant shaft can shift and fall out when the device is opened, potentially breaking the device. This may cause the implant to become ineffective or cause injury if not properly fixed.
Patients who received the recalled implants are most at risk. The recall affects individuals who have the specific model numbers and lot numbers listed in the recall notice.
Check the product for model numbers 110019010 and lot numbers including 017350, 141990, 142000, 142020, 167190, 240720, 240740, 240770, 257970, 398710, 398730, 398740, 398750, 421780, 421790, 421800, 465910, 504120, 813190, 940370.
Identify the model number and lot numbers on the device to confirm if it is affected.
The implant shaft can shift and fall out during device opening, potentially breaking the device.
Check for model number 110019010 and lot numbers listed in the recall notice.
The recall does not specify a remedy, so contact Zimmer Biomet directly 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-1009-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-1009-2018 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.
