Medical Action Industries, Inc. 306 recall: Kit: Epidural/Pain TQC 20/Cs and 1 more product
Medical Action Industries, Inc. 306 is recalling Kit: Epidural/Pain TQC 20/Cs and 1 more product because of a sterility problem – 1,960; 3,606. The U.S. Food and Drug Administration published the recall on September 16, 2026; it began on July 23, 2026. Distributed in 6 states (Florida, Iowa, Kansas, Missouri, Ohio, Virginia).
Most serious Class I is the most serious level: a reasonable probability that using or eating the product will cause serious health problems or death.
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| Product | Kit: Epidural/Pain TQC 20/Cs and 1 more product |
| Brand | Medical Action Industries, Inc. 306 |
| Type | Medical devices |
| Classification | Class I |
| Recall date | July 23, 2026 |
| Published by FDA | September 16, 2026 |
| Quantity | 1,960; 3,606 |
| Recall ID | 99613 |
Recalled products (2)
- Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules
- FDA recall number
- Z-3106-2026
- Codes, lots and dates
- 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
- 1,960
- Classification
- Class I
- 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
- FDA recall number
- Z-3107-2026
- 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
- Classification
- Class I
Identifiers and details
- FDA event ID
- 99613
- Initiated
- Voluntary: Firm initiated
- Status
- Ongoing
- Firm location
- Arden, NC, United States
Why it was recalled
The problem: a sterility problem.
The reason the FDA lists: “Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.”
Where it was sold
6 states: Florida, Iowa, Kansas, Missouri, Ohio, Virginia. Distribution as the FDA records it: “US distribution to states of: IA, VA, MO, KS, FL, OH and LS.”
What to do
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Official notice: FDA Enforcement Report record (event 99613, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.
Other Medical Action Industries, Inc. 306 recalls
| Date | Recall | Problem | Agency |
|---|---|---|---|
| Sep 23, 2026 |  Medical Action Industries, Inc. 306 recall: Blood Culture Collection Venipuncture Kit 20/CsMedical devices · 6,420 | Blood culture convenience kits contain a component subject to a drug recall that due to an… Serious | FDA Class II |
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| Date | Recall | Problem | Agency |
|---|---|---|---|
| Oct 7, 2026 | Draeger recall: VentStar Resus NeoMedical devices · 1,063,643 units | Potential cracks in the hose, which could lead to leakage or the hose falling off. Most serious | FDA Class I |
| Oct 7, 2026 | Medline Industries recall: Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories and 1 more productMedical devices · 771,127 total | a fire hazard Most serious | FDA Class I |
| Oct 7, 2026 | Karl Storz Endoscopy recall: HOPKINS Telescope 30¿Medical devices · 6 eyepieces | Due to incorrect inside packaging label for eyepiece. Serious | FDA Class II |
| Oct 7, 2026 | Noxbox recall: NOxBOXi Nitric Oxide Delivery SystemMedical devices · 1,667 units | Potential for irregular oxygen readings due to a manufacturing issue affecting certain oxy… Serious | FDA Class II |
| Oct 7, 2026 | Siemens Healthcare Diagnostics recall: Atellica CH Revised C-Reactive ProteinMedical devices · 42940 units (3938 US, 39002 OUS) | The potential for falsely elevated results. Serious | FDA Class II |
| Oct 7, 2026 | Tandem Diabetes Care recall: T:slim Mobile ApplicationMedical devices · 177 | A beta (early-release) version of the iOS application, version 2.13 (TestFlight) had a sof… Serious | FDA Class II |
About this recall
Is Medical Action Industries, Inc. 306 Kit: Epidural/Pain TQC 20/Cs recalled?
Yes. Medical Action Industries, Inc. 306 recalled it on July 23, 2026; FDA published it September 16, 2026 (Class I). Only the lots, dates or models listed on this page are included.
Why was it recalled?
Because of a sterility problem. The reason given: Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.
What should I do if I have it?
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Where was it sold?
In 6 states (Florida, Iowa, Kansas, Missouri, Ohio, Virginia).
More recalls
Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.