ClearanceBrief
Recall Z-2010-2023 ยท MBF Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented

Limacorporate S.p.A

REF 1975.14.800, Prima TT Genoid Modular Reverse TT Baseplate, Sterile R

DateJun 27, 2023 (initiated May 30, 2023)
StatusOpen, Classified
ReasonDue to manufacturing issue, their is a potential for peripheral holes to be out of specification.
Root causeDevice Design
ActionOn May 30, 2023 LimaCorporate issued an Urgent: Medical device Recall notification via E-Mail. LimaCorporate asked consignees to take the following actions: 1. Check your stock to locate and quarantine the affected devices. Devices must be sent back to your Lima local reference within 15 days together with a hard copy of the attached Response Form at the following address: Lima U.S.A., Inc. | 2001 NE Green Oaks Blvd. Ste.100 | Arlington, Texas 76006 | USA 2. Fill out, sign and send the attached Response Form via email to your Lima local reference at uscomplaint@limacorporate.com as a confir
Quantity13 units
DistributionUS Nationwide distribution in the states of MI, IL, ND, MO, OK.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K222427PRIMA TT Glenoid
Lima Corporate S.P.A., Oct 6, 2022