Recall Z-0123-2026— B BRAUN MEDICAL INC
Class II · Ongoing
Class II FDA medical device recall by B BRAUN MEDICAL INC, initiated 2025-09-18. FDA's recall record names no specific 510(k) clearance for this event. Product: Combined Spinal and Epidural Anesthesia Tray, PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle, PENCAN 27 Ga. x 5 in. (12.7 cm) Spinal Needle and 19 Ga. Open Tip PERIFIX FX Springwound Epidural Catheter. Product Code: NES1727KFX. Product Description: NES1727KFX W /17GA TUOHY 19GA SPRW OT.. Reason: Potential for the lid of the catheter connector to be in the incorrect position..
- Recalling firm
- B BRAUN MEDICAL INC
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2025-09-18
- Firm location
- Allentown, PA, United States
Product description
Combined Spinal and Epidural Anesthesia Tray, PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle, PENCAN 27 Ga. x 5 in. (12.7 cm) Spinal Needle and 19 Ga. Open Tip PERIFIX FX Springwound Epidural Catheter. Product Code: NES1727KFX. Product Description: NES1727KFX W /17GA TUOHY 19GA SPRW OT.
Reason for recall
Potential for the lid of the catheter connector to be in the incorrect position.
Data sourced from openFDA. This site is unofficial and independent of the FDA.