Recall Z-3181-2026— Medical Action Industries, Inc. 306
Class II · Ongoing
Class II FDA medical device recall by Medical Action Industries, Inc. 306, initiated 2026-07-23. FDA's recall record names no specific 510(k) clearance for this event. 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. 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..
- Recalling firm
- Medical Action Industries, Inc. 306
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2026-07-23
- Firm location
- Arden, NC, United States
Product description
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
Reason for recall
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.