Kit: Epidural/Pain TQC 20/Cs recall (Medical Action Industries, Inc. 306)
Medical deviceClass IOngoing
Summary: Medical Action Industries, Inc. 306 is recalling Kit: Epidural/Pain TQC 20/Cs, REF: 82465 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: Epidural/Pain TQC 20/Cs, REF: 82465 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
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)
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-3106-2026 |
| 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 | 1,960 |
More recalls from Medical Action Industries, Inc. 306 · all medical device recalls · recalls from July 2026