# FDA recall Z-0124-2026

> **B BRAUN MEDICAL INC** · Class II · device recall initiated 2025-09-18.

## Product

Design Options, Pain Management Tray. Product Code: SESK. Product Descriptions:   1. SESK PARKLAND MEMORIAL FX CSE TRAY.     2. SESK OWENSBORO DAVIESS HOSP 20058814.    3. SESK MEMORIAL HEALTH SYSTEM SPINAL/EPID.    4. SESK ST. JOHN'S MERCY MED CTR SPINAL/EPID.    5. SESK MAIMONIDES HOSPITAL SPINAL/EPIDURAL.    6. SESK OU MEDICAL CENTER - SPINAL/EPIDURAL.    7. SESK ELLIS HOSPITAL - SPINAL EPIDURAL.    8. STONY BROOK HSP SPINAL EPIDRAL TRAY SESK.     9. SESK UAB SPINAL EPIDURAL.    10. SESK CREIGHTON UNIV BMH SOINAL EPIDURAL.    11. SESK, BSW SPINAL EPIDURAL TRAY.     12. LYNDON B JOHNSON HOSPITAL SPINAL EPID.

## Reason for recall

Potential for the lid of the catheter connector to be in the incorrect position.

## Distribution

Nationwide distribution to AK, AL, AR, AZ, CA, CO, FL, GA, HI, IA, IL, IN, KS, LA, MA, MD, ME, MI, MN, MO, MS, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV.

## Key facts

- **Recall number:** Z-0124-2026
- **Recalling firm:** B BRAUN MEDICAL INC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-09-18
- **Report date:** 2025-10-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Allentown, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0124-2026

## Citation

> AI Analytics. FDA recall Z-0124-2026. Retrieved 2026-07-25 from https://api.ai-analytics.org/recall/Z-0124-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*