Combined Spinal and Epidural Anesthesia Tray, PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Nee
Pending LLM rewrite. Source: FDA_DEVICE Z-0123-2026.
Severity not yet assessed
We have not scored this recall against our rubric yet, so we are not showing a severity rating or our usual guidance. The agency’s own notice below is the authoritative source — read it first.
Plain-English summary
Potential for the lid of the catheter connector to be in the incorrect position.
The recalled product
- 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 T
- Manufacturer
- B BRAUN MEDICAL INC
- Category
- Medical Device — Devices
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (6)
- REF: 333197
- Product Code: NES1727KFX
- UDI-DI (Primary): 04046964179327
- UDI-DI (Unit of Use): 04046964179310
- Lot Numbers: 0062000732
- 0062012053. Expiration Date: 07/31/2026.
Distribution
Distributed nationwide across the United States.
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