FDA Device recall Z-3108-2018
Affixus¿ Hip Fracture Nail 130¿ 9 mm x 180 mm, Item Number: 814509180
- FDA Device
- Class II
- terminated
- Published 2018-09-19
On 2018-09-19 the FDA classified a Class II recall of Affixus¿ Hip Fracture Nail 130¿ 9 mm x 180 mm, Item Number: 814509180 by Zimmer Biomet, citing the set screw is not able to advance or reverse from the original position in the nail.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3108-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-07-17 |
| Published | 2018-09-19 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Zimmer Biomet |
| Distribution | AL, AR, AZ, CA, CO, FL, GA, HI, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, SC, SD, TN, TX, UT, VA, WA, WI, WY |
Product
Affixus¿ Hip Fracture Nail 130¿ 9 mm x 180 mm, Item Number: 814509180
Reason
The set screw is not able to advance or reverse from the original position in the nail.
Identifiers
| code_info | 054130 085710 144520 150790 156740 156750 219790 245740 245820 287290 287400 456140 482650 707780 900280…054130 085710 144520 150790 156740 156750 219790 245740 245820 287290 287400 456140 482650 707780 900280 944590 944630 944640 970640 609640 609650 |
|---|
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-3108-2018%22
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