Presource Convenience Kits recall
Cardinal Health 200, LLC recalled Presource Convenience Kits on September 30, 2026 because of the kits contain applicators that may exhibit an open or incomplete seal on the packaging of the applicator. It was sold nationwide.
Why it was recalled
The kits contain applicators that may exhibit an open or incomplete seal on the packaging of the applicator. Use of a potentially contaminated applicator could result in no patient harm or may lead to localized skin or soft tissue infection. Less commonly, systemic infection or other infectious complications may occur.
What's recalled
Presource Convenience Kits: 1) KIT, USGPIV , Catalog Number: PVMHIVMHD; 2) KIT, USGPIV , Catalog Number: PVMHIVM14; 3) KIT, USGPIV , Catalog Number: PVMHIVM15
Quantity: 9480 kits
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- Cardinal Health 200, LLC, Waukegan, IL
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
US Nationwide distribution in the states of FL, KY, MO, NC, OH, TX. - Status
- Ongoing
- Recall number
- Z-3255-2026
- Source
- U.S. Food and Drug Administration
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