Z-1496-2014 Class II Terminated
FDA device recall Z-1496-2014 was initiated by Zimmer, Inc. on Apr 1, 2014 and is designated Class II. Reason for recall: The shell was missing the locking ring. The recall status is terminated (terminated Sep 11, 2014). Affected quantity: 17 units.
Recall Details
- Product Type
- Devices
- Report Date
- Apr 30, 2014
- Initiation Date
- Apr 1, 2014
- Termination Date
- Sep 11, 2014
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 17 units
Product Description
TRABECULAR METAL MODULAR ACETABULAR SYSTEM, Shell with Cluster Holes, Porous 60mm. Catalog number 00-6202-060-22; Hip implant component.
Reason for Recall
The shell was missing the locking ring.
Distribution Pattern
Worldwide Distribution: US (nationwide) in states of: US: GA, WI, NJ, CA, NY, NC, PA, FL, CT, ME, TX, and IL; and countries of: Australia and Canada.
Code Information
00-6202-060-22; lot 62490588
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1496-2014
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026