FDA Device recall Z-1522-2018
Orthopedic Salvage System (OSS) Modular Arthrodesis 0 Degree Locking Collar, Model Number CP260600 Product Usage: The replacement of segmen…
- FDA Device
- Class II
- terminated
- Published 2018-05-02
On 2018-05-02 the FDA classified a Class II recall of Orthopedic Salvage System (OSS) Modular Arthrodesis 0 Degree Locking Collar, Model Number CP260600 Product Usage: The replacement of segmen… by Zimmer Biomet, citing there is a potential dry blast irregularity on the locking collar screws packaged with the locking collar.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1522-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-04-03 |
| Published | 2018-05-02 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Zimmer Biomet |
| Distribution | CT, FL, GA, IN, MA, MI, NY, TX |
Product
Orthopedic Salvage System (OSS) Modular Arthrodesis 0 Degree Locking Collar, Model Number CP260600 Product Usage: The replacement of segmental defects of long bone, including midshaft replacement, and arthrodesis of the knee.
Reason
There is a potential dry blast irregularity on the locking collar screws packaged with the locking collar.
Identifiers
| code_info | Lot Number 360610, 333020 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1522-2018%22
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