Medical Action Industries recalls
3 federal recalls on file. We monitor every CPSC, FDA, USDA, and NHTSA notice for Medical Action Industries and translate it into plain English — free weekly digest, optional same-day alerts.
- 2026-09-23FDA-DeviceClass IIMedical Action blood culture kits recalled for packaging seal issues
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.
- 2026-09-16FDA-DeviceClass IMedical Action Industries epidural kits recalled for sterility risk
Medical Action Industries' Single Shot Epidural kits containing Sodium Chloride Injection ampules have been recalled because the sodium chloride ampules are subject to another recall due to potentially compromised sterility. The affected kits were distributed to hospitals and medical facilities in Iowa, Virginia, Missouri, Kansas, Florida, Ohio, and Louisiana.
- 2026-09-16FDA-DeviceClass IMedical Action epidural kit recalled for sterility risk
Medical Action Industries is recalling epidural and pain management kits (REF 82465) that contain sodium chloride ampules. The ampules are subject to a separate recall due to potentially compromised sterility, which could affect the safety of the kits.
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