FDA Device recall Z-1225-2022
PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK
- FDA Device
- Class II
- terminated
- Published 2022-06-08
On 2022-06-08 the FDA classified a Class II recall of PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK by Microport Orthopedics, citing one manufacturing lot is missing the plasma-spray coating in the proximal region of the stem body.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1225-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-05-04 |
| Published | 2022-06-08 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Microport Orthopedics |
| Distribution | US |
Product
PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK
Reason
One manufacturing lot is missing the plasma-spray coating in the proximal region of the stem body.
Identifiers
| code_info | Catalog Number(s): PHAPCLS7; Lot Number(s): 1903727; Expiration Date: 11/24/2029; UDI/DI Number: 00192629112773 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
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FDA Device · Class II · 2024-07-10 · Microport Orthopedics - EVOLUTION MP Tibial Bases, Size 2+ LEFT, REF ETPKN2PL, knee tibial base
FDA Device · Class II · 2023-02-22 · Microport Orthopedics - EVOLUTION MP Tibial Bases, Size 7 LEFT, REF ETPKN7SL, knee tibial base
FDA Device · Class II · 2023-02-22 · Microport Orthopedics
All Microport Orthopedics recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1225-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.