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