Z-2131-2014 Class II Terminated
FDA device recall Z-2131-2014 was initiated by Zimmer, Inc. on Jun 10, 2014 and is designated Class II. Reason for recall: A complaint was received in which it was reported that an 8-hole plate from lot 62276042 had an enlarged hole that is unable to lock the screw, which resulted in the screw head pulling through plate… The recall status is terminated (terminated Jan 9, 2015). Affected quantity: 28 units.
Recall Details
- Product Type
- Devices
- Report Date
- Aug 6, 2014
- Initiation Date
- Jun 10, 2014
- Termination Date
- Jan 9, 2015
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 28 units
Product Description
Zimmer Periarticular Locking Plate System Distal Radial Volar Plate Lateral Column (1st generation stainless steel only). Orthopedic fixation plate. For temporary internal fixation and stabilization of osteotomies and fractures.
Reason for Recall
A complaint was received in which it was reported that an 8-hole plate from lot 62276042 had an enlarged hole that is unable to lock the screw, which resulted in the screw head pulling through plate hole.
Distribution Pattern
Worldwide Distribution - US including the states of CA and OH., and the countries of BRAZIL, CHINA, KOREA and TAIWAN.
Code Information
Part Number 00-2358-014-04; lot 62276042
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2131-2014
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026