Recall archive / 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. Source coverage and dates.
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
What the recall classes mean. 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.
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.