RecallRadar

FDA Device recall Z-3120-2018

Affixus¿ Hip Fracture Nail 130¿ 11 mm x 180 mm, Item Number: 814511180

On 2018-09-19 the FDA classified a Class II recall of Affixus¿ Hip Fracture Nail 130¿ 11 mm x 180 mm, Item Number: 814511180 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

AgencyFDA Device
Recall numberZ-3120-2018
ClassificationClass II
Statusterminated
Initiated2018-07-17
Published2018-09-19
Last updated2026-09-13 11:54 UTC
CompanyZimmer Biomet
DistributionAL, 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¿ 11 mm x 180 mm, Item Number: 814511180

Reason

The set screw is not able to advance or reverse from the original position in the nail.

Identifiers

code_info
072620 130760 130770 130780 130790 130800 130810 130820 130840 130850 130860 130900 130920 131030 156770…072620 130760 130770 130780 130790 130800 130810 130820 130840 130850 130860 130900 130920 131030 156770 157000 188340 219800 219810 219820 219910 245570 245690 287090 287120 287130 371170 456160 519490 530110 530120 530130 558980 565870 565880 601390 707920 768050 772730 854270 901300 901330 901350 901360 901370 901380 901400 901410 944660 944720 970790 970810 970820 970830 970840 970850 970860 970870 970880 970890 130930 130940 156970 503980 503990 504000 504010

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-3120-2018%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.