Skip to content
Recall Observatory FDA recall evidence

Device product

R3 (TM) XLPE ACETABULAR LINER UHMWPE, 20o OVERHANG, 36 MM ID, 62 MM OD, QTY: (1), STERILE H2O2, REF 71335762. Orthopaedic.

Z-1928-2013

May 29, 2013

Class II

Product summary

Firm
Smith & Nephew Inc
Event
Event 65370
Status
Terminated
Classification
Class II
Quantity
53 units
Official record key
device-enforcement:Z-1928-2013

Official wording

Reason: One batch of 60 mm 20o R3 XLPE liner may be laser etched and packaged as a 62 mm 20o liner and one batch of 62 mm 20o R3 XLPE liner may be laser etched and packaged as a 60 mm 20o liner.

Code information: Batch No. 12FM00603

Distribution pattern: Worldwide Distribution-USA including the states of PA, WA, TX, FL, IA, MI, WI, TN, KY, IN, NY, MO and OR, and the countries of India, Canada, Chile, Venezuela, Dubai, South Africa, Australia, Poland, Romania, Belgium, Germany and United Kingdom.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    One batch of 60 mm 20o R3 XLPE liner may be laser etched and packaged as a 62 mm 20o liner and one batch of 62 mm 20o R3 XLPE liner may be laser etched and packaged as a 60 mm 20o liner.