DePuy LifeLiner Stick & Cut Resistant Gloves Rt — Class III medical device recall Z-1331-2013
Terminated recall by DePuy Orthopaedics, Inc., reported 2013-05-22, distributed nationwide. LifeLiner Stick and Cut Resistant Gloves are being recalled because cases and individual glove packages were m
| Recall number | Z-1331-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | DePuy Orthopaedics, Inc., Warsaw, IN, United States |
| Recall initiated | 2013-05-08 |
| Classified | 2013-05-16 |
| Reported by FDA | 2013-05-22 |
| Terminated | 2014-01-14 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, GB, NL |
| Lot numbers | D12178C |
| Model numbers | 5200-68-000 |
Product
DePuy LifeLiner Stick & Cut Resistant Gloves Rt, Lg Part No. 5200-68-000 The gloves are designed to resist sticks and cuts and are not cut or puncture proof. These gloves are not required by any surgical technique.
Reason for recall
LifeLiner Stick and Cut Resistant Gloves are being recalled because cases and individual glove packages were mispackaged, with right handed, large sized glove packaging containing left handed, large sized gloves.
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-1331-2013. 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.