OMNIlife science Inc. Recall: OMNIlife science, Inc. ApeX acetabular liner hip prosthesis
OMNIlife science Inc. Recall: OMNIlife science, Inc. ApeX acetabular liner hip prosthesis is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: OMNIlife science Inc.; Product: OMNIlife science, Inc. ApeX acetabular liner hip prosthesis component Serf Dual Mobility Cup Insert Liner 51-28; Pro
| Recalling firm | OMNIlife science Inc. |
|---|---|
| Product | OMNIlife science, Inc. ApeX acetabular liner hip prosthesis component Serf Dual Mobility Cup Insert Liner 51-28; Product code: H6-25128 |
| Reason for recall | Acetabular liners failed the oxidation testing performed prior to release. They may experience a higher wear rate, leading to revision surgery. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | US nationwide distribution to states of: IL, NY, OK, MD, AL, PA, CO, FL, and UT. |
| Recall initiated | 20190723 |
| Recall number | Z-2480-2019 |
| Category | device |
| State | MA |
| Country | United States |
$29/mo
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