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Recall Observatory FDA recall evidence

Device product

SMR Shoulder/Spalla Trial Humeral Head diameter .42 mm, REF 9013.22.425; SMR Shoulder/Spalla Trial Humeral Head diameter .44 mm, REF 9013.22.445; SMR Shoulder/Spalla Trial Humeral Head diameter .46 mm, REF 9013.22.465; for use in shoulder implant surgery.

Z-2539-2015

August 14, 2015

Class II

Product summary

Firm
Limacorporate S.p.A
Event
Event 71972
Status
Terminated
Classification
Class II
Quantity
110 units
Official record key
device-enforcement:Z-2539-2015

Official wording

Reason: The dimensions of the mating features of the recalled products are out of specification causing the device to be difficult to assemble.

Code information: Lot Numbers: 14AA234, 14AA235, 14AA233

Distribution pattern: US Distribution to the states of: OH, TX, NC, NY, CA, FL, KS, AL, MI, MT, CO, MO, NV, WA, MN and LA., and Internationally to Australia.

Derived failure modes

  • Potency or specification failure

    reason.potency_specification_failure · v1.0.0

    out of specification