FDA Device recall Z-1169-2020
SPECIALIST 2 DISTAL FEMORAL CUTTING BLOCK. Part code 966115
- FDA Device
- Class II
- terminated
- Published 2020-02-19
On 2020-02-19 the FDA classified a Class II recall of SPECIALIST 2 DISTAL FEMORAL CUTTING BLOCK. Part code 966115 by Depuy Orthopaedics, citing the device will not connect to the Specialist 2 Locating Outrigger which renders them unusable in surgery.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1169-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-01-03 |
| Published | 2020-02-19 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Depuy Orthopaedics |
| Distribution | IA, MA, NY, OH, PA |
Product
SPECIALIST 2 DISTAL FEMORAL CUTTING BLOCK. Part code 966115. The product is a femoral cutting block.
Reason
The device will not connect to the Specialist 2 Locating Outrigger which renders them unusable in surgery.
Identifiers
| code_info | Lot SO2040929 ***Updated 7/9/20*** Lot SO2040602 Lot SO2037408 (None of this lot distributed in the US / OUS distribution only) |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1169-2020%22
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