Cardinal Health recalls AAMI 3 surgical gowns with unknown bioburden and contamination risks. Affected gowns may pose health hazards during medical procedures. Consumers should contact the manufacturer for details.
The gowns contain an unknown level of bioburden, unknown microbiological flora, and unknown particulate contamination.
Cardinal Health is recalling AAMI 3 non-reinf surgical gowns with unknown levels of bioburden and contamination. These gowns could pose health risks during medical procedures if used improperly.
The gowns contain unknown levels of bioburden, microbiological flora, and particulate contamination. This could lead to health risks if the gowns are used in medical procedures without proper sterilization.
Healthcare workers and patients who use the recalled surgical gowns during medical procedures are most at risk due to potential contamination.
Check for the item code 9545 on the gown. Lot numbers follow specific patterns: for 2018 production, the month code J (September) through M (December) are affected; for 2019 production, all lot numbers are affected.
Reach out to Cardinal Health for specific details about your gown's lot number and whether it's affected.
The recall states the gowns contain unknown levels of bioburden and contamination, so they are not considered safe for medical use without further verification.
Check the lot number on the gown. For 2018 production, lot numbers with month codes J through M are affected; for 2019 production, all lot numbers are affected.
Contact Cardinal Health directly for guidance on whether to discard or return the gown.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-1033-2020 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-1033-2020 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.
