Reported Oct 15, 2025 · Ongoing

Design Options, Pain Management Tray. Product Code: SESK. Product Descriptions: 1. SESK PARKLAND MEMORIAL FX CSE TRAY.…

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?

12 of 12 products

Products covered by this recall
#Product as published
1SESK PARKLAND MEMORIAL FX CSE TRAY.
2SESK OWENSBORO DAVIESS HOSP 20058814.
3SESK MEMORIAL HEALTH SYSTEM SPINAL/EPID.
4SESK ST. JOHN'S MERCY MED CTR SPINAL/EPID.
5SESK MAIMONIDES HOSPITAL SPINAL/EPIDURAL.
6SESK OU MEDICAL CENTER - SPINAL/EPIDURAL.
7SESK ELLIS HOSPITAL - SPINAL EPIDURAL.
8STONY BROOK HSP SPINAL EPIDRAL TRAY SESK.
9SESK UAB SPINAL EPIDURAL.
10SESK CREIGHTON UNIV BMH SOINAL EPIDURAL.
11SESK, BSW SPINAL EPIDURAL TRAY.
12LYNDON B JOHNSON HOSPITAL SPINAL EPID.
Lot codes and dates

12 of 12 products

Products covered by this recall
Model / numberBarcodesProduct as published
5300290404696430524504046964305238Product Code: SESK; UDI-DI (Primary): 04046964305245; UDI-DI (Unit of Use): 04046964305238; Lot Number: 0062012031.
5300480404696430531304046964305306Product Code: SESK; UDI-DI (Primary): 04046964305313; UDI-DI (Unit of Use): 04046964305306; Lot Number: 0062006298.
5301550404696430621104046964306204Product Code: SESK; UDI-DI (Primary): 04046964306211; UDI-DI (Unit of Use): 04046964306204; Lot Number: 0062012054.
5301590404696466928604046964669279Product Code: SESK; UDI-DI (Primary): 04046964669286; UDI-DI (Unit of Use): 04046964669279; Lot Number: 0062012025.
5301690404696480892004046964808913Product Code: SESK; UDI-DI (Primary): 04046964808920; UDI-DI (Unit of Use): 04046964808913; Lot Number: 0062012035.
5301710404696495039104046964950384Product Code: SESK; UDI-DI (Primary): 04046964950391; UDI-DI (Unit of Use): 04046964950384; Lot Number: 0062006303.
5301800404695515644304046955156436Product Code: SESK; UDI-DI (Primary): 04046955156443; UDI-DI (Unit of Use): 04046955156436; Lot Number: 0062000738.
5301970404695561933704046955619320Product Code: SESK; UDI-DI (Primary): 04046955619337; UDI-DI (Unit of Use): 04046955619320; Lot Number: 0062003710.
53019440469555893884046955589371Product Code: SESK; UDI-DI (Primary): 4046955589388; UDI-DI (Unit of Use): 4046955589371; Lot Number: 0062014360.
5301990404695561937504046955619368Product Code: SESK; UDI-DI (Primary): 04046955619375; UDI-DI (Unit of Use): 04046955619368; Lot Number: 0062001876.
5301600404696481399304046964813986Product Code: SESK; UDI-DI (Primary): 04046964813993; UDI-DI (Unit of Use): 04046964813986; Lot Number: 0062011011.
5301840404695515652804046955156511Product Code: SESK; UDI-DI (Primary): 04046955156528; UDI-DI (Unit of Use): 04046955156511; Lot Number: 0062003228. Expiration Date: 07/31/2026.
Amount recalled
2,450 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.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new B Braun Medical Inc. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:33 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.