---
title: "Perifix¿ / Epidural anesthesia set, medicated — FDA record Z-2627-2023 | Is It on Recall"
description: "Product may be mislabeled with an incorrect lid stock label."
url: https://isitonrecall.com/recall/fda-device-z-2627-2023-perifix-epidural-anesthesia-set-medicated/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Perifix¿ / Epidural anesthesia set, medicated — FDA record Z-2627-2023

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 31, 2023. 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**: Perifix¿ / Epidural anesthesia set, medicated
- **Reason**: Product may be mislabeled with an incorrect lid stock label.
- **Classification**: Class II
- **Recalling firm**: B. Braun Medical, Inc.
- **Quantity**: 3440 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2627-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2627-2023%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 | UDI-DI: 04046964178726 Product Code: 332250; Lot Number 0061863524, expiration date 30.APR.2025 |

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

## Distribution

US Distributions to states of - AR, AZ, CA, FL, GA, IL, MA, MO, NC, NJ, PA, TX, WA

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

- [Arkansas](https://isitonrecall.com/state/arkansas/)
- [Arizona](https://isitonrecall.com/state/arizona/)
- [California](https://isitonrecall.com/state/california/)
- [Florida](https://isitonrecall.com/state/florida/)
- [Georgia](https://isitonrecall.com/state/georgia/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [Massachusetts](https://isitonrecall.com/state/massachusetts/)
- [Missouri](https://isitonrecall.com/state/missouri/)
- [North Carolina](https://isitonrecall.com/state/north-carolina/)
- [New Jersey](https://isitonrecall.com/state/new-jersey/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [Texas](https://isitonrecall.com/state/texas/)
- [Washington](https://isitonrecall.com/state/washington/)

## Dates in the source

- **Report date**: Sep 27, 2023
- **Recall initiation date**: Jul 31, 2023
- **Center classification date**: Sep 21, 2023

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-2627-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [B. Braun Medical, Inc. records](https://isitonrecall.com/brand/b-braun-medical-inc/)