FDAFDA recall Z-3107-2026 · Sep 16, 2026
Medical Action Industries, Inc. 306: Kit: Single Shot Epidural 20/Cs recall
Recall found
Product
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
Reason for recall
Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class I: FDA's most serious class, where use of or exposure to the product may cause serious health problems or death.
- Status
- Ongoing
- Codes, lots and dates
- 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)
- Quantity
- 3,606
- Distribution
- US distribution to states of: IA, VA, MO, KS, FL, OH and LS.
- Recalling firm
- Medical Action Industries, Inc. 306, Arden, NC
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-07-23
Source: openFDA enforcement record Z-3107-2026 · search recall number Z-3107-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.