Is Medical Action Industries, Inc. 306 recalled?

Yes — a recall has been published. Reason: Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.

SeriousFDAOngoing

Can cause serious harm or death.

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

Check the device or its packaging for

REF/UDI-DI/Lot(Expiration Date): 59553/10809160010518/330274(9/1/2026), 331036(11/1/2026), 332995(11/1/2026), 333957(11/1/2026), 338894(11/1/2026); 83945B/10809160444269/330827(10/10/2026), 330907(10/10/2026), 333956(11/1/2026), 350340(11/1/2026), 351266(11/30/2026), 373674(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: 16 September 2026This is the date the recall was announced. A company may have started it weeks earlier.
Recall began: 23 July 2026

Source: FDA record Z-3107-2026 · retrieved 9 September 2026

Read the official notice

Every recall is shown word for word from the FDA and USDA, with a link to the source.