Limacorporate S.p.A: Medical Device Recall in 2016 - (Recall #: Z-1711-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

SMR glenosphere impactor/extractor; Used to implant the glenosphere in the SMR Reverse Shoulder replacement.

Product Classification:

Class II

Date Initiated: April 8, 2016

Date Posted: June 1, 2016

Recall Number: Z-1711-2016

Event ID: 73870

Reason for Recall:

Complaints of intra-operative breakage of the glenosphere impactors/extractors.

Status: Terminated

Product Quantity: 314 units

Code Information:

Lot numbers: 1390763, 14AA094, 14AA431, 14AA528, 15AA094, 15AA557, 15AA558, 15AA559, 15AA600

Distribution Pattern:

Distributed US (nationwide) and in Australia.

Voluntary or Mandated:

Voluntary: Firm initiated