Howmedica Osteonics Corp. recalls Triathlon Pro Tibial Preparation Tray, Revision AC- for organization, storage, and transport in preparation for sterilization of…
Triathlon Pro Tibial Preparation Tray may have been kitted with the Triathlon Cemented #1-3 Keel Punch (P/N: 6541-2-013) instead of the Triathlon Pro #0-3 Cemented Keel Punch (P/N: 6541-2-013Y) instrument can lead to…
Read the official notice →- Date
- 2022-01-12
- Country
- United States
- Brand
- Howmedica Osteonics
- Product
- Triathlon Pro Tibial Preparation Tray, Revision AC- for organization, storage, and transport in preparation for sterilization of re-usable…
- Classification
- Class II
- Units
- US Nationwide distribution in the states of GA, MI, NC, TX.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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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Potential product mix where the size and/or offset of the Biolox delta Ceramic V40 Femoral Head inside the package does not match the package labeling
FDA · DeviceHowmedica Osteonics Corp.Worldwide distribution - US Nationwide distribution in the states of AZ, CA,…Official notice → - 2022-02-23
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Other drugs & medical recalls in the United States
- 2022-01-12
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Abbott Molecular, Inc. recalls Alinity m System, Part No. 08N53-002
There is a software defect that can cause the Amplification Detection clamp CLEAN position to be set too high.
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There is a software issue associated with the ability to properly complete a Field Service Engineer Maintenance and Diagnostics procedure.
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Uromedica Inc. recalls UROMEDICA Implantation Instrument Set (Sheath and Sharp Trocar), REF 750041, nonsterile.
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Device lacks premarket approval.
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