Z-1331-2013 Class III Terminated
FDA device recall Z-1331-2013 was initiated by DePuy Orthopaedics, Inc. on May 8, 2013 and is designated Class III. 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… The recall status is terminated (terminated Jan 14, 2014). Affected quantity: 180 gloves (120 gloves distributed in the US).
Recall Details
- Product Type
- Devices
- Report Date
- May 22, 2013
- Initiation Date
- May 8, 2013
- Termination Date
- Jan 14, 2014
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 180 gloves (120 gloves distributed in the US)
Product Description
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.
Distribution Pattern
Worldwide Distribution - US (nationwide) including the states of IL, OH, NC, SC, MN, NV, TN and WA., and the countries of UK, Netherlands and Canada.
Code Information
Lot - D12178C
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1331-2013
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026