Medical Action Industries, Inc. 306: Nerve Block Tray
Recall Summary Medical Action Industries is recalling Epidural/Pain TQC 20 nerve block kits (reference number 82465) distributed to Florida, Iowa, Kansas, Missouri, and Virginia because the sodium chloride solution ampules included in these kits were subject to a separate recall due to potential sterility issues. The recalled kits were used for epidural and pain management procedures.
- Recalling firm
- Medical Action Industries, Inc. 306
- Product
- Kit: Epidural/Pain TQC 20/Cs, REF: 82465 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/66e02329-bc60-4c27-9d62-71a8a20bdcab