---
title: "Kit: Single Shot Epidural 20/Cs, REF: 59553; Kit: Single Shot Epidural 20/Cs,... — FDA record Z-3107-2026 | Is It on Recall"
description: "Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility."
url: https://isitonrecall.com/recall/fda-device-z-3107-2026-kit-single-shot-epidural-20-cs-ref-59553-kit-single-shot-epidural-20-cs-ref-83945b-containing-sodium/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Kit: Single Shot Epidural 20/Cs, REF: 59553; Kit: Single Shot Epidural 20/Cs, REF: 83945B. Containing Sodium Chloride... — FDA record Z-3107-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jul 23, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: 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.
- **Classification**: Class I
- **Recalling firm**: Medical Action Industries, Inc. 306
- **Quantity**: 3,606
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-3107-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3107-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | 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) |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US distribution to states of: IA, VA, MO, KS, FL, OH and LS.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Florida](https://isitonrecall.com/state/florida/)
- [Iowa](https://isitonrecall.com/state/iowa/)
- [Kansas](https://isitonrecall.com/state/kansas/)
- [Missouri](https://isitonrecall.com/state/missouri/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Virginia](https://isitonrecall.com/state/virginia/)

## Dates in the source

- **Report date**: Sep 16, 2026
- **Recall initiation date**: Jul 23, 2026
- **Center classification date**: Sep 9, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3107-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Medical Action Industries, Inc. 306 records](https://isitonrecall.com/brand/medical-action-industries-inc-306/)