FDA Device recall Z-1123-2015
Ringloc+ Acetabular Shell Finned 52 mm, PN 16-104152, hip prosthesis component
- FDA Device
- Class II
- terminated
- Published 2015-02-25
On 2015-02-25 the FDA classified a Class II recall of Ringloc+ Acetabular Shell Finned 52 mm, PN 16-104152, hip prosthesis component by Biomet, citing biomet recalled the Mallory Head 4 Finned Acetabular Shell 50mm (Lot 364600) and Ringloc + Acetabular Shell Limited Hole Finned 52 mm (Lot 427840) following a mix up in packaging….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1123-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-01-09 |
| Published | 2015-02-25 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Biomet |
| Distribution | TX, VA |
Product
Ringloc+ Acetabular Shell Finned 52 mm, PN 16-104152, hip prosthesis component.
Reason
Biomet recalled the Mallory Head 4 Finned Acetabular Shell 50mm (Lot 364600) and Ringloc + Acetabular Shell Limited Hole Finned 52 mm (Lot 427840) following a mix up in packaging with the two.
Identifiers
| code_info | Catalog Number: 16-104152 Lot Number Identification: 427840 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1123-2015%22
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