FDA Device recall Z-1475-2018
ZMS Intramedullary Fixation Smooth Guide Wire 2.4 mm Diameter, 100 cm Length
- FDA Device
- Class II
- terminated
- Published 2018-05-02
On 2018-05-02 the FDA classified a Class II recall of ZMS Intramedullary Fixation Smooth Guide Wire 2.4 mm Diameter, 100 cm Length by Zimmer Biomet, citing potential failure of sterile packaging seal.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1475-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-03-26 |
| Published | 2018-05-02 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Zimmer Biomet |
| Distribution | US |
Product
ZMS Intramedullary Fixation Smooth Guide Wire 2.4 mm Diameter, 100 cm Length; Item Number: 47-2237-033-00
Reason
Potential failure of sterile packaging seal.
Identifiers
| code_info | Lot Numbers: 63715690 63780127 63787482 |
|---|
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-1475-2018%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.