| | Class 2 Device Recall Design Options, PERIFIX FX Epidural Anesthesia Tray. |  |
| Date Initiated by Firm | September 18, 2025 |
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| Date Posted | October 09, 2025 |
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| Recall Status1 |
Open3, Classified |
| Recall Number | Z-0126-2026 |
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| Recall Event ID |
97550 |
| Product Classification |
Epidural anesthesia kit - Product Code OGE
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| Product | 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. |
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| 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. |
Recalling Firm/
Manufacturer |
B BRAUN MEDICAL INC
861 Marcon Blvd
Allentown PA 18109-9577
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| For Additional Information Contact | Allison Longenhagen
001-484-2408373 |
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Manufacturer Reason
for Recall | Potential for the lid of the catheter connector to be in the incorrect position. |
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FDA Determined
Cause 2 | Process control |
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| Action | B Braun notified consignees on about 09/18/2025 via USPS certified mailed URGENT MEDICAL DEVICE CORRECTION NOTIFICATION. Consignees were instructed to, where possible, have a second kit or additional catheter connector available at the point of use and upon opening the kit, verify the correct catheter connector is present. If the affected component is detected, discard and do not use. Consignees were also instructed to review the Medical Device Correction Notification and ensure all users in your organization and other concerned persons are informed, if affected units have been further distributed, notify customers, post the notification where affected units are stored, and complete and return the "Urgent Medical Device Correction Acknowledgement Form." Additionally, if consignees have identified affected units in inventory, they may order one case (50 pieces) of affected sterilized single use catheter connectors to have on hand.
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| Quantity in Commerce | 5,770 units |
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| 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.
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| Total Product Life Cycle | TPLC Device Report |
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1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
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