OVERLOOKED

Recalls › Medicines & devices

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)

What to do

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)

  1. 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 I
  2. 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

    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

  1. 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

More Medicines & devices recalls