Cardinal Health recalls AAMI 3 RoyalSilk Surgical Gowns with unknown bioburden and microbiological contamination. Affected items have specific lot numbers from 2018-2019 production. Consumers should contact Cardinal Health for details.
The gowns contain an unknown level of bioburden, unknown microbiological flora, and unknown particulate contamination.
Cardinal Health is recalling AAMI 3 RoyalSilk Surgical Gowns that may contain unknown levels of bioburden and microbiological contamination. This could pose a health risk to users, especially in medical settings where sterile conditions are critical.
The gowns contain unknown levels of bioburden, unknown microbiological flora, and unknown particulate contamination. This could lead to infections or other health issues if the gowns are used in sterile medical procedures.
Healthcare professionals and surgical staff who use these gowns are most at risk due to potential contamination. Patients receiving procedures using these gowns could also be affected.
Check the lot number on the gown's label. For 2018 production, the lot number starts with 'J' followed by a month code (J=September, K=October, L=November, M=December). For 2019 production, all lot numbers are affected.
Look for the lot number on the gown's label to determine if it's affected. For 2018 production, the lot number starts with 'J' followed by a month code (J=September, K=October, L=November, M=December). For 2019 production, all lot numbers are affected.
Yes, all 2019 production gowns are affected.
If your gown was made in 2018, the lot number starts with 'J' followed by a month code (J=September, K=October, L=November, M=December).
Contact Cardinal Health for details on the remedy. The recall record does not specify a remedy.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-1013-2020 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-1013-2020 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.
