SeriousFDAOngoing
Can cause serious harm or death.
Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules
Check the device or its packaging for
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)
- Why
- Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.
- Distributed
- US distribution to states of: IA, VA, MO, KS, FL, OH and LS.
- Company
- Medical Action Industries, Inc. 306
- Announced
- This is the date the recall was announced. A company may have started it weeks earlier.
- Recall began
Source: FDA record Z-3106-2026 · retrieved 9 September 2026
Read the official notice