FDA Device recall Z-3132-2018
Affixus¿ Hip Fracture Nail 130¿ 13 mm x 180 mm, Item Number: 814513180
- 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¿ 13 mm x 180 mm, Item Number: 814513180 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-3132-2018 |
| 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¿ 13 mm x 180 mm, Item Number: 814513180
Reason
The set screw is not able to advance or reverse from the original position in the nail.
Identifiers
| code_info | 063590 063600 220020 245510 290720 371210 482750 482760 482770 523410 097180 188350 188370 290690 970510 970530 970580 |
|---|
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-3132-2018%22
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