FDA Device recall Z-1470-2018
ZMS Intramedullary Fixation Smooth Guide Wire 3.0 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 3.0 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-1470-2018 |
| 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 3.0 mm Diameter, 100 cm Length; Item Number: 47-2237-037-00
Reason
Potential failure of sterile packaging seal.
Identifiers
| code_info | Lot Numbers: 63662549 63668704 63696974 63709171 63721377 63731176 63764550 63771164 63781920 63803595 63812302 63817719 63826242 |
|---|
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-1470-2018%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.