FDA Device recall Z-1467-2018
Zimmer Natural Nail System Tear Drop Guide Wire 3.0 mm Diameter, 70 cm length
- FDA Device
- Class II
- terminated
- Published 2018-05-02
On 2018-05-02 the FDA classified a Class II recall of Zimmer Natural Nail System Tear Drop Guide Wire 3.0 mm Diameter, 70 cm length by Zimmer Biomet, citing potential failure of sterile packaging seal.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1467-2018 |
| 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
Zimmer Natural Nail System Tear Drop Guide Wire 3.0 mm Diameter, 70 cm length; Item Number: 47-2490-098-00
Reason
Potential failure of sterile packaging seal.
Identifiers
| code_info | Lot Numbers: 63631729 63638177 63645647 63645648 63662542 63681727 63690177 63690178 63733040 63733041 6373…Lot Numbers: 63631729 63638177 63645647 63645648 63662542 63681727 63690177 63690178 63733040 63733041 63733042 63748389 63753764 63758424 63771141 63780123 63787478 63826236 77006549 77006550 77006551 77006553 77006558 63836288 |
|---|
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-1467-2018%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.