Z-2483-2015 Class II Terminated
FDA device recall Z-2483-2015 was initiated by Biomet, Inc. on Jul 28, 2015 and is designated Class II. Reason for recall: The device was assembled without screw hole plugs. The recall status is terminated (terminated May 17, 2016). Affected quantity: 5.
Recall Details
- Product Type
- Devices
- Report Date
- Sep 9, 2015
- Initiation Date
- Jul 28, 2015
- Termination Date
- May 17, 2016
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 5
Product Description
Vision RingLoc Shell 50 mm Size 23. Hip joint replacement prosthesis.
Reason for Recall
The device was assembled without screw hole plugs.
Distribution Pattern
Distributed in Canada and Japan.
Code Information
Part Number:135250; Lot Number:946410
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2483-2015
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026