FDA Device recall Z-1152-2016
Product 54 consists of all product under product code: JWH and same usage: Item no: 596009900 NEXGEN TAPER PLUG for use in total knee arthr…
- FDA Device
- Class II
- terminated
- Published 2016-03-23
On 2016-03-23 the FDA classified a Class II recall of Product 54 consists of all product under product code: JWH and same usage: Item no: 596009900 NEXGEN TAPER PLUG for use in total knee arthr… 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-1152-2016 |
| 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 54 consists of all product under product code: JWH and same usage: Item no: 596009900 NEXGEN TAPER PLUG for use in total knee 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.: 61390872 61761213 61780493 61780494 61780495 61780496 61780497 61789111 61789112 61789113 61789114…lot no.: 61390872 61761213 61780493 61780494 61780495 61780496 61780497 61789111 61789112 61789113 61789114 61789115 61789116 61789117 61789118 61789119 61789120 61789121 61789122 61789123 61789124 61789125 61789126 61789127 61789128 61789129 61789130 61789131 61789132 61789133 61789134 61789135 61789136 61789137 61789138 61789139 61789140 61789141 61789142 61798737 61798738 61798739 61798740 61798741 61798742 61798743 61798744 61798745 61798746 61799383 61799384 61799385 61799386 61799387 61799388 61799389 61799390 61799391 61799392 61803606 61803607 61803608 61803609 61803610 61803611 61803612 61803613 61803614 61803615 61807320 61807321 61807322 61807323 61807324 61807325 61807326 61807327 61807328 61807329 61807330 61809795 61809796 61809797 61809798 61809799 61809801 61809802 61809803 61809804 61809805 61816959 61816960 61816961 61816962 61816963 61816964 61816965 61816966 61816967 |
|---|
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-1152-2016%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.