Class II FDA device recall · Z-0126-2026

Class II — the FDA judged the product may cause temporary or medically reversible harm, with a remote chance of serious harm.

This is the FDA's risk judgment for this recall. It describes the potential of the product as a category — it does not establish that any specific unit harmed anyone. Most recalls are Class II or III.

Design Options, PERIFIX FX Epidural Anesthesia Tray. Product Code: CESK. Product Descriptions: 1. CESK ROBERT WOOD JOHNSON UNIV HOSP. 2. CESK EAST JEFFERSON GEN HOSP 20071769. 3. CESK FLETCHER ALLEN HOSPITAL. 4. CESK WASHOE MEDICAL CENTER. 5. CESK DETROIT MEDICAL CTR 20064586. 6. CESK ALBANY MEDICAL CENTER. 7. CESK EPIDURAL BLOCK TRAY. 8. CESK, BSW EPIDURAL TRAY. 9. CESK HOWARD COUNTY GENERAL. 10. CESK CE17TKFC10L. 11. CESK WILLIAMSON MEDICAL CENTER. 12. CESK FLORIDA HOSPITAL. 13. CESK RIVERSIDE HEALTH SYSTEM. 14. CESK MAYO CLINIC OB. 15. CESK PRESBYTERIAN HOSPITAL DALLAS. 16. CESK HOUSTON METHODIST HOSPITAL. 17. CESK OHIO STATE UNIV MEDICAL CENTER. 18. CESK NORTONS WOMEN'S AND CHILDREN'S. 19. CESK BEN TAUB. 20. CESK PENN MEDICINE CONTINUOUS-ORIG CUST. 21. CESK ALLEGHENY GENERAL HOSPITAL. 22. CESK UNIVERSITY OF ILLINOIS MED CTR. 23. CESK RUSH UNIVERSITY MEDICAL CENTER. 24. CESK ST. JOSEPH MEDICAL CENTER. 25. CESK INTEGRIS HEALTH. 26. CESK UMASS MEMORIAL. 27. CESK STANFORD UNIV HOSP 20054718. 28. CESK OVERLAKE HOSPITAL. 29. CESK CHRIST HOSPITAL 20057985. 30. CESK NEWTON-WELLESLEY HOSPITAL.

Why it was recalled

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

Is your unit affected?

The recall covers only the specific lots or serial numbers the FDA listed. Enter the lot or serial number from your product's label and we'll check it against that list.

A match means your unit may be covered — stop and call your pharmacist before doing anything. No match suggests it isn't covered, but confirm anyway: code formats vary and lists can be incomplete. Your unit not being listed does not guarantee it is safe, and being listed does not mean you have been harmed.

Show the FDA's listed lot / code information

1. REF: 551028; Product Code: CESK; UDI-DI (Primary): 04046964306334; UDI-DI (Unit of Use): 04046964306327; Lot Number: 0062017630.  2. REF: 551474; Product Code: CESK; UDI-DI (Primary): 04046964306938; UDI-DI (Unit of Use): 04046964306921; Lot Number: 0062006292.  3. REF: 551630; Product Code: CESK; UDI-DI (Primary): 04046964307560; UDI-DI (Unit of Use): 04046964307546; Lot Number: 0062017605.  4. REF: 551749: Product Code: CESK; UDI-DI (Primary): 04046964307942; UDI-DI (Unit of Use): 04046964307935; Lot Number: 0062017615.   5. REF: 551769: Product Code: CESK; UDI-DI (Primary): 04046964308024; UDI-DI (Unit of Use): 04046964308017; Lot Number: 0062006304.   6. REF: 551998: Product Code: CESK; UDI-DI (Primary): 04046964310942; UDI-DI (Unit of Use): 04046964310928; Lot Number: 0062014368.   7. REF: 552006: Product Code: CESK; UDI-DI (Primary): 04046964311215; UDI-DI (Unit of Use): 04046964311192; Lot Number: 0062013265.   8. REF: 552076: Product Code: CESK; UDI-DI (Primary): 04046964814013; UDI-DI (Unit of Use): 04046964814006; Lot Number: 0062003111.   9. REF: 552113: Product Code: CESK; UDI-DI (Primary): 04046964950193; UDI-DI (Unit of Use): 04046964950186; Lot Number: 0062006384.   10. REF: 552116: Product Code: CESK; UDI-DI (Primary): 04046964950254; UDI-DI (Unit of Use): 04046964950247; Lot Number: 0061994277.   11. REF: 552119: Product Code: CESK; UDI-DI (Primary): 04046964989780; UDI-DI (Unit of Use): 04046964989773; Lot Number: 0062017951.   12. REF: 552123: Product Code: CESK; UDI-DI (Primary): 04046955057788; UDI-DI (Unit of Use): 04046955057771; Lot Number: 0062003214.   13. REF: 552126: Product Code: CESK; UDI-DI (Primary): 04046955056903; UDI-DI (Unit of Use): 04046955056897; Lot Number: 0061999998.   14. REF: 552133: Product Code: CESK; UDI-DI (Primary): 04046955127801; UDI-DI (Unit of Use): 04046955127795; Lot Number: 0062012017.   15. REF: 552135: Product Code: CESK; UDI-DI (Primary): 04046955127849; UDI-DI (Unit of Use): 04046955127832; Lot Number: 0062013246.   16. REF: 552136: Product Code: CESK; UDI-DI (Primary): 04046955127863; UDI-DI (Unit of Use): 04046955127856; Lot Number: 0062003706.   17. REF: 552147: Product Code: CESK; UDI-DI (Primary): 04046955184071; UDI-DI (Unit of Use): 04046955186402; Lot Number: 0062017607.   18. REF: 552152: Product Code: CESK; UDI-DI (Primary): 04046955214419; UDI-DI (Unit of Use): 04046955264407; Lot Number: 0062006313.   19. REF: 552153: Product Code: CESK; UDI-DI (Primary): 04046955214426; UDI-DI (Unit of Use): 04046955243037; Lot Number: 0062017625.   20. REF: 552174: Product Code: CESK; UDI-DI (Primary): 04046955589449; UDI-DI (Unit of Use): 04046955589432; Lot Number: 0062006317.   21. REF: 552176: Product Code: CESK; UDI-DI (Primary): 04046955589487; UDI-DI (Unit of Use): 04046955589470; Lot Number: 0061983245.  22. REF: 552177: Product Code: CESK; UDI-DI (Primary): 04046955596102; UDI-DI (Unit of Use): 04046955596096; Lot Number: 0062014364.   23. REF: 552179: Product Code: CESK; UDI-DI (Primary): 04046955596140; UDI-DI (Unit of Use): 04046955596133; Lot Number: 0062013260.   24. REF: 552180: Product Code: CESK; UDI-DI (Primary): 04046955596164; UDI-DI (Unit of Use): 04046955596157; Lot Number: 0062000125.   25. REF: 552192: Product Code: CESK; UDI-DI (Primary): 04046955701063; UDI-DI (Unit of Use): 04046955701056; Lot Number: 0062005198.   26. REF: 552197: Product Code: CESK; UDI-DI (Primary): 04046955862498; UDI-DI (Unit of Use): 04046955862481; Lot Number: 0062017634.   27. REF: 555098: Product Code: CESK; UDI-DI (Primary): 04046964313578; UDI-DI (Unit of Use): 04046964313554; Lot Number: 0062006293.   28. REF: 555422: Product Code: CESK; UDI-DI (Primary): 04046964315534; UDI-DI (Unit of Use): 04046964315503; Lot Number: 0062019003.   29. REF: 555450: Product Code: CESK; UDI-DI (Primary): 04046964315831; UDI-DI (Unit of Use): 04046964315817; Lot Number: 0062016181.   30. REF: 555484: Product Code: CESK; UDI-DI (Primary): 04046964315954; UDI-DI (Unit of Use): 04046964315930; Lot Number: 0062012043.   Expiration Date: 07/31/2026.

Recall status

Ongoing — the recall is still being carried out.

Where it was distributed

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.

Recall record

Recalling firm: B BRAUN MEDICAL INC
Product type: Devices
Recall number: Z-0126-2026
Voluntary / mandated: Voluntary: Firm initiated
Initial notification: Letter
Origin: Allentown, PA
Recall initiated: 2025-09-18

What to do

Check the lot/code above against your product. To confirm this record and read the FDA's full notice, see the FDA recall page. Before changing anything you take or use, ask your pharmacist or prescriber — this page does not tell you to start or stop any drug or device.

Also available: structured data (JSON-LD) · recall record (JSON)

What this is — and is not

A recall is a recorded FDA enforcement action — the FDA logged that a firm is removing or correcting a product. It does not establish that any specific unit harmed anyone, and causation is not established by a recall. The class above is the FDA's risk judgment for the product category, not a finding about your unit. This page informs and compares; it is not medical advice and never tells you to start or stop a drug or device.

To report a problem you experienced, use FDA MedWatch. Verify this record at FDA recalls · Recall Z-0126-2026 · Source: openFDA enforcement.