PlainRecalls
FDA Devices Moderate Class II Ongoing

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

Reported: February 8, 2023 Initiated: November 29, 2022 #Z-1036-2023

Product Description

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

Reason for Recall

Product missing the four small locking collar bolts resulting in extension of surgery to find a replacement

Details

Recalling Firm
Biomet, Inc.
Units Affected
2 units
Distribution
US Nationwide distribution in the states of CA, KY, FL.
Location
Warsaw, IN

Frequently Asked Questions

What product was recalled?
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. Recalled by Biomet, Inc.. Units affected: 2 units.
Why was this product recalled?
Product missing the four small locking collar bolts resulting in extension of surgery to find a replacement
Which agency issued this recall?
This recall was issued by the FDA Devices on February 8, 2023. Severity: Moderate. Recall number: Z-1036-2023.