Zimmer Biomet recalls Orthopedic Salvage System (OSS) Modular Arthrodesis 0 Degree Locking Collar Model CP260600 due to potential dry blast irregularity in locking collar screws.
There is a potential dry blast irregularity on the locking collar screws packaged with the locking collar.
Zimmer Biomet is recalling a specific orthopedic implant model because of a potential dry blast irregularity in the locking collar screws. This could affect the safety and proper function of the device during knee surgery.
The locking collar screws may have a dry blast irregularity, which could lead to improper fitting or function during knee surgery. This might cause complications if the implant does not work as intended.
Patients who received the Orthopedic Salvage System (OSS) Modular Arthrodesis 0 Degree Locking Collar with model number CP260600 are likely affected. Surgeons and medical facilities using this specific implant are at the highest risk.
Check for the model number CP260600 on the Orthopedic Salvage System (OSS) Modular Arthrodesis 0 Degree Locking Collar. The product was sold with lot numbers 360610 and 333020.
Identify the model number CP260600 and lot numbers 360610 or 333020 on the device.
The recall is for a potential dry blast irregularity in the locking collar screws, which could affect surgical function but does not indicate immediate serious injury risk.
The official recall does not specify a remedy, so contact Zimmer Biomet directly for guidance.
Look for model number CP260600 and lot numbers 360610 or 333020 on the Orthopedic Salvage System (OSS) Modular Arthrodesis 0 Degree Locking Collar.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-1522-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-1522-2018 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.
