FDA Device recall Z-1023-2014
MODULAR CUP NEUTRAL LINER MODULAR CUP 10 DEGREE LIN MODULAR CUP 20 DEGREE LIN MODULAR CUP 7MM OFFSET LI
- FDA Device
- Class II
- terminated
- Published 2014-02-26
On 2014-02-26 the FDA classified a Class II recall of MODULAR CUP NEUTRAL LINER MODULAR CUP 10 DEGREE LIN MODULAR CUP 20 DEGREE LIN MODULAR CUP 7MM OFFSET LI by Zimmer, citing zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. (ZMBV) facility in Ponce, Puerto Rico. Based on this review, it was deter….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1023-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-10-11 |
| Published | 2014-02-26 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Zimmer |
| Distribution | US |
Product
MODULAR CUP NEUTRAL LINER MODULAR CUP 10 DEGREE LIN MODULAR CUP 20 DEGREE LIN MODULAR CUP 7MM OFFSET LI
Reason
Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. (ZMBV) facility in Ponce, Puerto Rico. Based on this review, it was determined that the packaging operations conducted in the Building 1 packaging operation at this facility were not properly validated. As a result, Zimmer conducted seal integrity testing to evaluate if previously packaged product from this facility met the established requirements for sterile barrier integrity. The acceptance criteria established for this testing was 99% reliability with a 90% confidence interval. These packaging tray configurations met the acceptance criteria for sterile barrier integrity of both the inner and outer trays, however, Zimmer has decided to recall all manufacturing lots that have not expired and that were sterile packaged in the ZMBV facility Building 1 packaging operations.
Identifiers
| code_info | 61547919 61954158 61241463 61821673 62188365 61564304 60919205 61666604 60928241 62086340 62296755 60611445…61547919 61954158 61241463 61821673 62188365 61564304 60919205 61666604 60928241 62086340 62296755 60611445 60841757 60863748 61187640 61224727 61261826 62062929 62173370 60550153 60588810 60828784 61018862 61110916 61159634 62296754 60576173 61209715 61564309 60575226 60595581 60623653 60749578 62316407 60611447 61255394 61364450 61382532 60611244 60817929 60863723 60563186 62268497 61547941 62137191 61892712 61901662 60668061 61584777 61059234 61403759 60497031 61303608 61875716 62087621 62138394 61906179 61919744 61853252 60945780 61403762 61868301 62123088 62330868 61552276 60973584 61159666 61209871 61491267 61731038 61906430 62154608 60806194 60940002 61092880 62304925 61598585 61698771 61712665 61902214 62148657 60612251 60658071 60980492 61072064 61160052 61261860 61642713 61722445 62296659 60715034 61018915 61036921 61136634 61179946 61377132 61504792 61564330 61598593 61652828 |
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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-1023-2014%22
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