Medical Action Industries, Inc. 306 recalls Kit: Epidural/Pain TQC 20/Cs
- Recalling company
- 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 I – a reasonable probability that use will cause serious adverse health consequences or death
- Recall date
- Jul 23, 2026
- Reported
- Sep 16, 2026
- Distribution
- US distribution to states of: IA, VA, MO, KS, FL, OH and LS.
- Status
- Ongoing
- Quantity
- 1,960
- Lot / codes
- UDI-DI: 10809160367414. Lot(Expiration Date): 322200(4/1/2026), 324586(4/1/2026), 327335(4/1/2026), 329618(9/1/2026), 347199(11/1/2026), 337283(11/1/2026), 350354(11/30/2026), 375449(5/31/2027)
- Company location
- Arden, NC
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-3106-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-3106-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.