Medical Action Industries, Inc. 306: Spinal Epidural Anesthesia Kit
- Recalling firm
- Medical Action Industries, Inc. 306
- 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
- Reason
- Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-07-23
- Status
- Open, Classified
- Areas affected
- FL, IA, KS, MO, VA
- Distribution
- US distribution to states of: IA, VA, MO, KS, FL, OH and LS.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/3336c41c-d1e3-41a6-96a1-8e3d6b60e69a