FDA Device recall Z-2090-2013
Free Lock Femoral Hip Fixation System Compression Lag Screw . Several lengths (55 to 150 mm) and diameters (12.7 and 15. 8 mm)
- FDA Device
- Class II
- terminated
- Published 2013-09-04
On 2013-09-04 the FDA classified a Class II recall of Free Lock Femoral Hip Fixation System Compression Lag Screw . Several lengths (55 to 150 mm) and diameters (12.7 and 15. 8 mm) by Zimmer, citing single packaging configuration used for the VERSA-FX-II Femoral Fixation System failed the leak test compromising the sterility of the product.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2090-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-06-19 |
| Published | 2013-09-04 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Zimmer |
| Distribution | US |
Product
Free Lock Femoral Hip Fixation System Compression Lag Screw . Several lengths (55 to 150 mm) and diameters (12.7 and 15. 8 mm). Item codes starting with 00-1181-05, 00-1181-10 and 00-1181-15. ZIMMER Compression Hip Screw, orthopedic implant.
Reason
Single packaging configuration used for the VERSA-FX-II Femoral Fixation System failed the leak test compromising the sterility of the product.
Identifiers
| code_info | 60621340 60621339 60621342 60621345 60639475 60621341 60621338 60621344 60671954 60653031 60653066 60671958…60621340 60621339 60621342 60621345 60639475 60621341 60621338 60621344 60671954 60653031 60653066 60671958 60639474 60653032 60653043 60653053 60653063 60671956 60671957 60705048 60653057 60653069 60671955 60621343 60705047 60714810 60705044 60701995 60705045 60701998 60702002 60705043 60702006 60680439 60736748 60781210 60781213 60781212 60781211 60782044 60782047 60782049 60705046 60714808 60782048 60782043 60782050 60736749 60714809 60736750 60782046 60736752 60736753 60736756 60782040 60782045 60736754 60781209 60782041 60812142 60812145 60782037 60812143 60812147 60815943 60564710 60812146 60817011 60782042 60812141 60812144 60812148 60815946 60830649 60830650 60830670 60830652 60572991 60736755 60736758 60862361 60862362 60862363 60862364 60862365 60862366 60862367 60879681 60862369 60879678 60862368 60564708 60915347 60931209 60931208 60931211 60931212 60931213 60931215 60973693 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2090-2013%22
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