Official recall record
Presource Convenience Kits: 1) KIT, USGPIV , Catalog Number: PVMHIVMHD; 2) KIT, USGPIV , Catalog Numb
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2026-08-10
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 10197106488959
- Brand on record
- Cardinal Health 200, LLC
- Product category
- Medical Device
What the authority reported
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 to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-10-22.
Record last checked against the registry on 2026-10-22.
Other recalls from this brand
- 2026-08-19 · US FDA — Medical Devices
Presource Packs containing Medtronic Microstream Components: Intubation Kit Catalog Numbers AN23366084 - 2026-08-18 · US FDA — Medical Devices
Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT, LAP CHOLE , Catal - 2026-08-18 · US FDA — Medical Devices
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All 31 official recall notices naming Cardinal Health 200, LLC on this site →
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