← Search recalls
FDA (Device enforcement)Recalled 2025-09-18class ii

B BRAUN MEDICAL INC: PERIFIX FX Continuous Epidural Anesthesia Set, PERIFIX Tuohy Epidural Needle - 17 Ga. x 3-1/2 in. (8.9 cm) - Winged, PERIFIX FX Springwound Epidural Catheter - 19 Ga. Closed tip.

Hazard

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

Details from the source

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. Quantity: 0 units Lot/code info: REF: 332238; Product Code: CE17TFC; UDI-DI (Primary): 04046964178603; UDI-DI (Unit of Use): 04046964178597; Lot Number: 0062014626. Expiration Date: 05/31/2028.

UPC codes

04046964178603, 04046964178597

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

Hurt by this product? Start a free Case Check

ProductRisk is not a law firm and does not provide legal services or legal advice. ProductRisk is a free consumer product-safety information service operated by Plaintify, Inc., a technology company. If you ask to be connected with a law firm, any legal services are provided by that firm — not by ProductRisk or Plaintify.

Privacy · Plaintify