Perifix® 332290Recalls & reported problems
B. Braun Medical Inc. · PERIFIX® 18 Ga. x 2 in. (50 mm) Tuohy, PERIFIX ONE 20 Ga. Closed Tip Catheter, 5 mL Glass Luer Slip LOR Tray (Kit) - Pediatric Tray · Class 2
All models of Perifix (57)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04046964179006), received between Nov 25, 2025 and Nov 25, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 25, 2025Break; Break
AS REPORTED BY THE USER FACILITY: REASON OF COMPLAINT: THE EPIDURAL CATHETER INFUSION PUMP INITIALLY RAN WITHOUT ISSUE, THOUGH OFF SINCE OCCLUSION ALARM AND RESISTANCE TO FLUSH NOTED AT 1527. PER DISCUSSION WITH PROCEDURAL TEAM, UNEVENTFUL PLACEMENT, LOR-2 CM, CATHETER EASILY ADVANCED WITHOUT RESISTANCE, SECURED - 10CM W/ GLUE AND INFUSION INITIALLY RAN WITHOUT ISSUES. PATIENT REPOSITIONED ON THE LEFT SIDE AND CATHETER ASSESSED. NO APPARENT KINKING, ASPIRATION NEGATIVE SIGNIFICANT RESISTANCE TO FLUSH ATTEMPT. CATHETER DRESSING TAKEN DOWN FOR FARTHER EVALUATION. INSERTION SITE, SURROUNDING SKIN, AND CATHETER ALL APPEARING UNREMARKABLE. CATHETER STILL INTACT AND SECURE WITH SKIN GLUE AT 12 CM EASILY WITHDRAWN TO 10 CM, CONTINUED RESISTANCE TO FLUSH ATTEMPT AT INSERTION SITE AND FRACTURED TIP NOTED AT SKIN. REMAINDER COMPONENT OF CATHETER IS NOT PALPABLE ON EXAM AND INSERTION SITE APPEARS UNREMARKABLE. ESTIMATED LENGTH OF RETAINED CATHETER IS 8 CM.
Patient problems: Foreign Body In Patient
MAUDE report 23649452 ↗
Other Epidural anesthesia kit devices
- Design Options® 552116B. Braun Medical Inc. · Epidural anesthesia kit2 recalls7 reports
- Design Options® 552126B. Braun Medical Inc. · Epidural anesthesia kit2 recalls0 reports
- Design Options® 552179B. Braun Medical Inc. · Epidural anesthesia kit2 recalls0 reports
- Design Options® 552177B. Braun Medical Inc. · Epidural anesthesia kit2 recalls0 reports
- Perifix® 332079B. Braun Medical Inc. · Epidural anesthesia kit1 recall45 reports
- Perifix® 332097B. Braun Medical Inc. · Epidural anesthesia kit1 recall39 reports
- Perifix® 332220B. Braun Medical Inc. · Epidural anesthesia kit1 recall21 reports
- Perifix® 332078B. Braun Medical Inc. · Epidural anesthesia kit1 recall12 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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