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FDA (Device enforcement)Recalled 2026-07-23class i

Medical Action Industries, Inc. 306: 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

Is my product affected?

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

  • UPC 10809160010518
  • UPC 10809160444269

Check against the official notice below — it lists the full affected range.

Hazard

Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.

Details from the source

Reason for recall: Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility. Distribution: US distribution to states of: IA, VA, MO, KS, FL, OH and LS. Quantity: 3,606 Lot/code info: 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)

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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