Becker® 24146Recalls & reported problems
Medtronic Ps Medical, Inc. · EDMS 24146 BECKER NO Y-SITE · Class 2
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00763000333423), received between Nov 26, 2024 and Nov 26, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Disconnection” (1 report).
1 FDA recall record name this device's identifier, 1 still open.
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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Recalls naming this device
- Nov 1, 2024Open, Classified
Due to complaints received reporting cracks and/or leaks of the stopcocks associated with the external drainage and monitoring system (EDMS).
Z-0661-2025 · Root cause: Under Investigation by firm · FDA record ↗
Most reported problems
Device problems
- Disconnection1
- Fluid/Blood Leak1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 26, 2024Disconnection; Fluid/Blood Leak; Disconnection; Fluid/Blood Leak
MEDTRONIC RECEIVED INFORMATION REGARDING AN EXTERNAL DRAINAGE AND MONITORING SYSTEM. IT WAS REPORTED THAT THE PATIENT'S DRAIN SYSTEMS FAILED CAUSING CEREBROSPINAL FLUID TO DRAIN DIRECTLY ON THE FLOOR. THE TUBING CONNECTED TO THE BOTTOM OF THE BURETTE WAS PARTIALLY DISCONNECTED. THE PRODUCT WAS REPLACED WITH ANOTHER DRAIN. THE TUBING OF THE SECOND DRAIN DISCONNECTED ENTIRELY FROM THE BOTTOM OF THE BURETTE BUT WAS REATTACHED BY THE NURSE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20785792 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.