Howmedica Osteonics Corp. recalls UNITRAX Endoprosthesis Head Component - 43mm. Implantable component used in partial hip arthroplasty. Catalog Number: 6942-5-043
Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis Head Component potentially may not match the device within the packaging. This product mix only involves the three (3) sizes (43mm, 42mm, and the…
Read the official notice →- Date
- 2024-07-24
- Country
- United States
- Brand
- Howmedica Osteonics
- Product
- UNITRAX Endoprosthesis Head Component - 43mm. Implantable component used in partial hip arthroplasty. Catalog Number: 6942-5-043
- Classification
- Class II
- Units
- Worldwide distribution - US Nationwide and the countries of Australia, Hong…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
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FDA · DeviceHowmedica Osteonics Corp.US Nationwide distribution in the states of AZ, FL, NC, OH, PA, TN, WI.…Official notice → - 2024-09-04
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- US
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FDA · DeviceHowmedica Osteonics Corp.Nationwide Foreign: Netherlands, Canada, Singapore, Spain, Sweden, UKOfficial notice → - 2024-03-13
- US
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Potential packaging breaches of inner blister and outer sterile blister.
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Other drugs & medical recalls in the United States
- 2024-07-24
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