Avanos Medical recalls Ballard Closed Suction Catheters model 227-5 due to lack of sterility assurance. Affected units may pose infection risks if used without proper sterilization.
Lack of sterility assurance for closed suction catheter systems
Avanos Medical recalls Ballard Closed S:227-5 suction catheters because they lack sterility assurance. Using these catheters without proper sterilization could lead to infections.
The catheters lack sterility assurance, meaning they may not be properly cleaned or sterilized before use. This increases the risk of infections if used without adequate sterilization procedures.
Healthcare providers using Ballard Closed Suction Catheters model 227-5 for adult patients are affected. Those in medical settings handling these catheters are at higher risk.
Check for model number 227-5 on the Ballard Closed Suction Catheters. Lot numbers 1555468 or serial numbers 00609038989655 and 10609038989652 are affected.
Verify if the catheters have been properly sterilized before use to reduce infection risk.
The recall indicates a lack of sterility assurance, so they may not be safe without proper sterilization procedures.
The recall does not specify a remedy, so check with your healthcare provider for safe handling practices.
Affected units have model number 227-5 and lot numbers 1555468 or serial numbers 00609038989655 and 10609038989652.
We’ve drafted a message you can send Ballard to request your refund or repair — edit it as you like.
Subject: Recall Z-1527-2025 — Ballard Ballard Hello, I own a Ballard that is covered by recall Z-1527-2025 from Ballard. 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.
