FDA-Device2026-09-23Class IIPACKAGING DEFECT

Medical Action Industries blood culture kits recalled for compromised sterile packaging

OTHERNationwide distributionMedical devices

What this means

Blood culture collection kits made by Medical Action Industries contain BD ChloraPrep applicators with potentially open or incomplete seals on their packaging. This compromised seal may allow contamination, and use of affected applicators could result in localized skin or soft tissue infection.

  • Check if you have affected kits: REF 77451, 81834B, or 81834C with lot numbers listed in the recall notice.
  • Do not use affected kits for blood culture collection.
  • Contact Medical Action Industries or your supplier for replacement or return instructions.
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The agency's original wording
Hazard

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.

Intended for
Adults
Illnesses reported
None reported
Sold states
US Nationwide distribution in the states of OH, IN, NC.
Affected count
6,420
Manufactured in
25 Heywood Rd, N/A, Arden, NC, United States
Products
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

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3181-2026

More Medical Action Industries recalls

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