Class IOngoing
Medical Action Industries, Inc. 306 recalls 2 products
Recall date · record updated Sep 16, 2026 · Source: U.S. Food and Drug Administration (openFDA device enforcement)
Check your product against the names and codes above. The FDA enforcement record lists the recall as voluntary: firm initiated; it does not state a consumer remedy, so follow the firm’s notice or the FDA link.
- Company
- Medical Action Industries, Inc. 306
- Reason
- Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.
- Hazard
- FDA Class I: a reasonable probability that use or exposure will cause serious adverse health consequences or death (FDA definition).
- Who’s affected
- US distribution to states of: IA, VA, MO, KS, FL, OH and LS.
- Where
- Florida, Iowa, Kansas, Missouri, Ohio, Virginia
- Official notice
- www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99613…
Products (2)
Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules
Codes/lots: 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)Quantity: 1,960Recall no. Z-3106-2026Class IKit: Single Shot Epidural 20/Cs, REF: 59553; Kit: Single Shot Epidural 20/Cs, REF: 83945B. Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules
Codes/lots: 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: 3,606Recall no. Z-3107-2026Class I
Update history
- First listed on OVERLOOKED from the official record.
When the agency expands or changes this recall, we update this page and log the change here.
Proof: raw official record (JSON) · fetched from FDA API
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