FDA Device recall Z-1466-2018
Humeral Guide Wire Ball Tip 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 Humeral Guide Wire Ball Tip 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-1466-2018 |
| 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
Humeral Guide Wire Ball Tip 2.4 mm Diameter 70 cm Length; Item Number: 47-2255-008-00
Reason
Potential failure of sterile packaging seal.
Identifiers
| code_info | Lot Numbers: 63738593 63738594 63738595 63738596 63748395 63748396 63748397 63748398 63753767 63753768 6375…Lot Numbers: 63738593 63738594 63738595 63738596 63748395 63748396 63748397 63748398 63753767 63753768 63758425 63758428 63771163 77006530 77006531 77006532 77006533 77006534 77006535 77006536 77006537 77006538 77006539 77006540 77006541 77006542 77006543 77006544 77006545 |
|---|
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-1466-2018%22
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