Zimmer Biomet recalls Orthopedic Salvage System Hybrid Poly Tibia Item #151813 due to potential ineffective cleaning processes. Affected products were distributed from June 2016 to February 2019.
Cleaning processes potentially being ineffective
Zimmer Biomet is recalling a specific orthopedic implant product because its cleaning processes might not work properly. This could lead to contamination or infection risks for patients using the device.
The cleaning processes for this orthopedic implant might not be effective, potentially leading to contamination or infection. This is a risk during medical procedures where the device is used.
Patients who received the Orthopedic Salvage System Hybrid Poly Tibia Item #151813 between June 2016 and February 2019 are likely affected. Healthcare providers using this product for surgeries are at higher risk.
Check for the product name 'Orthopedic Salvage System (OSS) Hybrid Poly Tibia' and item number #151813. Products were distributed between June 2016 and February 2019.
Identify if your product matches the description: Orthopedic Salvage System Hybrid Poly Tibia Item #151813.
The recall states that cleaning processes might be ineffective, which could lead to contamination or infection risks. However, the hazard is not described as causing serious injury in normal use.
Products were distributed between June 2016 and February 2019.
The recall does not specify a remedy, so no action is required beyond checking if you have the affected product.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-2234-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-2234-2019 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.