Biomet, Inc. OSS Modular Arthrodesis Nail, 7 Degree Collar Assembly with Locking Bolts-For use in the replacement of segmental defects of long bone, including midshaft replacement, and arthrodesis of the knee Item Number: CP260602 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
OSS Modular Arthrodesis Nail, 7 Degree Collar Assembly with Locking Bolts-For use in the replacement of segmental defects of long bone, including midshaft replacement, and arthrodesis of the knee Item Number: CP260602
Brand
Biomet, Inc.
Lot Codes / Batch Numbers
UDI: (01)00880304082991(17)321103(10)136620 Lot Number: 136620
Products Sold
UDI: (01)00880304082991(17)321103(10)136620 Lot Number: 136620
Biomet, Inc. is recalling OSS Modular Arthrodesis Nail, 7 Degree Collar Assembly with Locking Bolts-For use in the replacement due to Product missing the four small locking collar bolts resulting in extension of surgery to find a replacement. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Product missing the four small locking collar bolts resulting in extension of surgery to find a replacement
Recommended Action
Per FDA guidance
****UPDATE***Phase II Zimmer Biomet issued Urgent Medical Device Recall Letter (Removal) on March 7, via FedEx to the Distributor and Risk Manager. Letter states health risk and action to take: Risk Manager Responsibilities: 1. Review this notification and ensure that affected personnel are aware of the contents. 2. If you have affected product at your facility, assist your Zimmer Biomet sales representative and quarantine all affected product. Your Zimmer Biomet sales representative will remove the affected product from your facility. 3. If the product has been further distributed, provide your customers with the recall notice for hospitals and ensure documentation. 4. Complete Attachment 1 Certificate of Acknowledgement and send to CorporateQuality.PostMarket@zimmerbiomet.com. This form shall be returned even if you do not have affected products at your facility. 5. Retain a copy of the acknowledgement form with your recall records in the event of a compliance audit of your facility s documentation. If you have further questions or concerns after reviewing this notice, please call customer service at 574-371-3071 between 8:00 am and 5:00pm EST, Monday through Friday. Calls received outside of call center operating hours will receive a voicemail prompt or be transferred to an on-call representative in the event of an emergency. Alternatively, your questions may be emailed to CorporateQuality.PostMarket@zimmerbiomet.com. Zimmer Biomet is conducting the recall in a phased approach due to limited replacement products for the Modular Arthrodesis Nail Collar Assembly (PN: CP260602) and due to the ability to separately purchase the small locking collar bolts (PN: CP260603).Letter to Distributors via email on 11/29/22 states: Replacement Small Locking Collar Bolts (Part Number: CP260603) will be sent to your territory. Replacement orders were placed today, November 29, with overnight delivery to your main territory office (Phase 1) Once replacement devices are availab
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026