B Braun Medical recalled 2,840 NES1727KFX anesthesia tray kits distributed nationwide to healthcare facilities. The recall cites a potential mispositioned lid on the catheter connector. Healthcare providers should stop using the device immediately and follow recall instructions.
Potential for the lid of the catheter connector to be in the incorrect position.
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact B BRAUN MEDICAL INC or your healthcare provider for instructions. Notification method: Letter
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This product is an anesthesia tray kit used for combined spinal and epidural anesthesia in surgical settings.
A mispositioned catheter connector lid could lead to improper connections during anesthesia administration.
This recall is not described as part of a broader industry pattern.
Healthcare facilities must halt use of the affected kits and arrange for replacement, potentially affecting procedure scheduling and supply chain until replacements are received.
Recall notice from B Braun Medical and FDA enforcement page Z-0123-2026
Refunds or replacements expected within weeks per recall processes
Keep the recall notice, model/lot numbers, photos of the device, and all correspondence with the manufacturer for records
Product Code: NES1727KFX; Product Description: NES1727KFX W /17GA TUOHY 19GA SPRW OT..; Model: NES1727KFX; REF: 333197; UDI-DI (Primary): 04046964179327; UDI-DI (Unit of Use): 04046964179310; Lot Numbers: 0062000732, 0062012053; Quantity: 2,840 units; 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.
No injuries or incidents have been reported.
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