Limacorporate S.p.A Via Nazionale 52 Di San Daniele San Daniele Del Friuli Italy REF 1975.14.800, Prima TT Genoid Modular Reverse TT Baseplate, Sterile R Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
REF 1975.14.800, Prima TT Genoid Modular Reverse TT Baseplate, Sterile R
Brand
Limacorporate S.p.A Via Nazionale 52 Di San Daniele San Daniele Del Friuli Italy
Lot Codes / Batch Numbers
UDI-DI: 08033390244893, All Lots
Products Sold
UDI-DI: 08033390244893; All Lots
Limacorporate S.p.A Via Nazionale 52 Di San Daniele San Daniele Del Friuli Italy is recalling REF 1975.14.800, Prima TT Genoid Modular Reverse TT Baseplate, Sterile R due to Due to manufacturing issue, their is a potential for peripheral holes to be out of specification.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Due to manufacturing issue, their is a potential for peripheral holes to be out of specification.
Recommended Action
Per FDA guidance
On 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 confirmation that You have read and acknowledged the content of this FSN. 3. If If needed, please address any inquiry to the email address medicalcomplaints@limacorporate.com.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026