Class II — Medical Action Industries, Inc. 306
| Recalling firm | Medical Action Industries, Inc. 306 |
|---|---|
| Classification | Class II |
| Status | Ongoing |
| Reason | Blood culture convenience kits contain a component subject to a drug recall that due to an an open or incomplete seal on the packaging of the applicator may compromise the component's sterile barrier and if used may lead to localized skin or soft tissue infection. |
| Product | Blood Culture Collection Venipuncture Kit 20/Cs, REF: 77451; Blood Culture Kit 20/Cs, REF: 81834B; Blood Culture Collection Kit, REF: 81834C. All containing BD ChloraPrep Clear - 1 mL Applicators |
| Quantity | 6,420 |
| Distribution | US Nationwide distribution in the states of OH, IN, NC. |
| Initiated | 2026-07-23 |
| Classified | 2026-09-16 |
| Recall number | Z-3181-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Medical Action Industries, Inc. 306 (Z-3181-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/99628/
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