Cardinal Health recalls Presource Kit Total Joint Pack with double-wrapped basin component due to sterility assurance validation issues. Affected units sold with specific lot numbers.
The double wrapping of this custom kit basin set is not supported by the current sterility assurance validation.
Cardinal Health is recalling Presource Kit Total Joint Pack products that contain a double-wrapped basin component. This recall is due to a potential sterility risk that could affect patient safety during joint replacement procedures.
The double wrapping of the basin component in this kit may not meet sterility assurance standards. This could lead to contamination risks during surgical procedures, potentially affecting patient safety.
Patients undergoing joint replacement knee or hip procedures who use the recalled Presource Kit Total Joint Pack are affected. Healthcare providers using the kit for surgical procedures are at risk.
Check for lot numbers 104405, 122:2793, and 987948 on the Presource Kit Total Joint Pack. The product is used for joint replacement knee or hip surgeries.
Look for lot numbers 104405, 122793, or 987948 on the Presource Kit Total Joint Pack.
The double wrapping of the basin component may not meet sterility assurance validation standards, potentially leading to contamination risks during surgical procedures.
Check for lot numbers 104405, 122793, or 987948 on the Presource Kit Total Joint Pack, which is used for joint replacement knee or hip surgeries.
The recall record does not specify a remedy, so contact Cardinal Health for further instructions.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-0702-2019 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-0702-2019 from Cardinal Health. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
