FDA Device recall Z-1468-2018
Zimmer Natural Nail System Tear Drop Guide Wire 2.4 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 2.4 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-1468-2018 |
| 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 2.4 mm Diameter, 70 cm length; Item Number: 47-2490-098-01
Reason
Potential failure of sterile packaging seal.
Identifiers
| code_info | Lot Numbers: 63733044 63748390 63748391 77006546 77006547 77006548 |
|---|
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-1468-2018%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.