Data Foundry

Medical device recalls 2014

VerSys¿ Hip System — Class II medical device recall Z-1842-2014

Terminated recall by Zimmer, Inc., reported 2014-07-02, distributed nationwide. During routine inspection, beaded hip stem forgings received from supplier failed to meet ZES 2A-102. Processi

Recall numberZ-1842-2014
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmZimmer, Inc., Warsaw, IN, United States
Recall initiated2014-05-19
Classified2014-06-20
Reported by FDA2014-07-02
Terminated2015-03-24
DistributedNationwide (US)
Countries outside the USCA, CO, DO, JP, KR, PE, TH, TW
Quantity147 units
Lot numbers62472423, 62478967, 62479742, 62489572, 62496464, 62496469, 62503408, 62503411, 62509385, 62515502, 62522386, 62528282, 62530786, 62530790, 62544885, 62544907, 62544915, 62547211, 62547216, 62547217, 62554360, 62554362, 62587079, 62594428, 62622893, 62622894
Model numbers784301108, 784301126, 784301156, 784301208, 784301226, 784301256, 784301326, 784301356, 784301382, 784301511, 784301581

Product

VerSys¿ Hip System, Beaded Fullcoat Stems, Zimmer, Inc., Warsaw, IN 46581

Reason for recall

During routine inspection, beaded hip stem forgings received from supplier failed to meet ZES 2A-102. Processing of Beaded CoCrMo Alloy Hip Stem, material requirements per ATS #14-04818 and ATS #14-05549, respectively.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1842-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.