FDA Device recall Z-1164-2016
Product 66 consists of all product under product code: JDI and same usage: Item no: 785001100 VERSYS ADVOCATE CEMENTED 785001200 VERSYS ADV…
- FDA Device
- Class II
- terminated
- Published 2016-03-23
On 2016-03-23 the FDA classified a Class II recall of Product 66 consists of all product under product code: JDI and same usage: Item no: 785001100 VERSYS ADVOCATE CEMENTED 785001200 VERSYS ADV… by Zimmer Manufacturing B V, citing as a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1164-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-01-11 |
| Published | 2016-03-23 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Zimmer Manufacturing B V |
| Distribution | US |
Product
Product 66 consists of all product under product code: JDI and same usage: Item no: 785001100 VERSYS ADVOCATE CEMENTED 785001200 VERSYS ADVOCATE CEMENTED 785001220 VERSYS ADVOCATE CEMENTED 785001300 VERSYS ADVOCATE CEMENTED 785001320 VERSYS ADVOCATE CEMENTED 785001400 VERSYS ADVOCATE CEMENTED 785001420 VERSYS ADVOCATE CEMENTED 785001500 VERSYS ADVOCATE CEMENTED 785001520 VERSYS ADVOCATE CEMENTED 785001600 VERSYS ADVOCATE CEMENTED 785001620 VERSYS ADVOCATE CEMENTED 785001700 VERSYS ADVOCATE CEMENTED 785001305 VERSYS ADVOCATE V-LIGN CE 785001325 VERSYS ADVOCATE V-LIGN CE 785001405 VERSYS ADVOCATE V-LIGN CE 785001505 VERSYS ADVOCATE V-LIGN CE 785001525 VERSYS ADVOCATE V-LIGN CE For use in total or hemi hip arthroplasty
Reason
As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
Identifiers
| code_info | lot no.: 61983708 62030926 62033221 62036882 62036883 62038355 62075338 62075339 62075340 62097036 62097037…lot no.: 61983708 62030926 62033221 62036882 62036883 62038355 62075338 62075339 62075340 62097036 62097037 62122103 62122104 62154556 62166260 62171392 62171393 62177323 62178289 62181449 62183156 62183157 62188303 62189403 62192487 62193425 62195517 62204536 62206537 62210448 62216685 62222761 62240269 62240270 62240788 62240789 62240790 62240791 62279094 62280474 62284491 62299105 62312497 62312498 62314646 62315889 62317930 62318766 62320172 62324102 62326110 62346579 62354651 61809115 61820812 61911428 62018462 62027424 62028727 62028729 62042580 62042581 62050972 62050973 62050974 62166258 62166259 62167379 62167380 62174631 62174632 62178288 62181453 62186369 62186370 62186371 62194586 62199409 62204537 62210449 62222760 62234477 62234482 62240279 62240792 62240793 62251959 62252977 62252978 62255125 62280475 62284492 62284493 62306522 62306523 62317924 62317925 62317926 62320174 |
|---|
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-1164-2016%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.