Kit: Single Shot Epidural 20/Cs recall (Medical Action Industries, Inc. 306)
Medical deviceClass IOngoing
Summary: Medical Action Industries, Inc. 306 is recalling 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: Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.
What is being recalled
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
Why
Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.
How serious is it
Class I is the most serious level: FDA considers there is a reasonable probability that using or being exposed to this product will cause serious health problems or death.
Where it was sold
US distribution to states of: IA, VA, MO, KS, FL, OH and LS. (states named: Florida, Iowa, Kansas, Missouri, Ohio, Virginia)
How to tell if yours is affected
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)
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-3107-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class I |
| Status | Ongoing |
| Recall started | July 23, 2026 |
| Reported | September 16, 2026 |
| Company | Medical Action Industries, Inc. 306 |
| Company location | Arden, NC, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 3,606 |
More recalls from Medical Action Industries, Inc. 306 · all medical device recalls · recalls from July 2026