Reported Oct 15, 2025 · Ongoing
PERIFIX FX Continuous Epidural Anesthesia Set, PERIFIX Tuohy Epidural Needle - 17 Ga. x 3-1/2 in. (8.9 cm) - Winged,…
B Braun Medical Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: B BRAUN MEDICAL INC · 861 Marcon Blvd · Allentown, PA · 18109-9577
Is this the product you have?
- 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
- Product CodeCE17TFC
- Product DescriptionCE17TFC CONTINUOUS EPID SET W/17G TUOHY
- Lot codes and dates
- REF332238
- Product CodeCE17TFC
- UDI-DI (Primary)04046964178603
- UDI-DI (Unit of Use)04046964178597
- Lot Number0062014626
- Expiration Date05/31/2028
- Amount recalled
- 0 units
This recall covers 13 products
The agency filed one notice per product. You are reading one of them; the other 12 are below.
Where it was sold
Why it was recalled
Potential for the lid of the catheter connector to be in the incorrect position.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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