Howmedica Osteonics Corp. Recall: PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee r
Howmedica Osteonics Corp. Recall: PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee r is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Howmedica Osteonics Corp.; Product: PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Product Number: 6742-1-411; Reason for recal
| Recalling firm | Howmedica Osteonics Corp. |
|---|---|
| Product | PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Product Number: 6742-1-411 |
| Reason for recall | Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Ongoing |
| Distribution | Nationwide Foreign: Argentina, Australia, Brazil, Canada, Chile, China, Columbia, India, Japan, Korea, Latin America, Mexico, Poland, Sweden, Switzerland, Taiwan, UK, & Venlo (Netherlands). ***Updated 1/25/24*** Foreign distribution added: Austria, Finland, Germany, Ireland, Hong Kong, New Zealand, |
| Recall initiated | 20231201 |
| Recall number | Z-0923-2024 |
| Category | device |
| State | NJ |
| Country | United States |
$29/mo
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