Class I — Medical Action Industries, Inc. 306
| Recalling firm | Medical Action Industries, Inc. 306 |
|---|---|
| Classification | Class I |
| Status | Ongoing |
| Reason | Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility. |
| Product | Kit: Single Shot Epidural 20/Cs, REF: 59553; Kit: Single Shot Epidural 20/Cs, REF: 83945B. Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules |
| Quantity | 3,606 |
| Distribution | US distribution to states of: IA, VA, MO, KS, FL, OH and LS. |
| Initiated | 2026-07-23 |
| Classified | 2026-09-09 |
| Recall number | Z-3107-2026 |
| 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 I recall — Medical Action Industries, Inc. 306 (Z-3107-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/99613/
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