CORE DYNAMICS CD950Recalls & reported problems
Conmed Corporation · 5 MM ASPIRATION/INJECTION NEEDLE, 16 GAUGE, 40 CM LENGTH · Class 1
All models of CORE DYNAMICS (6)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 20653405043321), received between Mar 24, 2016 and Apr 27, 2017 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Detachment Of Device Component” (2 reports).
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.
Most reported problems
Device problems
- Detachment Of Device Component2
Patient problems
- No Known Impact Or Consequence To Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryApr 27, 2017Detachment Of Device Component; Detachment Of Device Component
AS REPORTED BY THE USER FACILITY, A 5MM CD950 WAS USED DURING A LAPAROSCOPIC CHOLECYSTECTOMY ON (B)(6) 2017. THE SCRUB NURSE NOTICED THAT THE BLUE END WAS DETACHED WHEN THE DEVICE WAS REMOVED FROM THE ABDOMEN PRIOR TO CLOSURE OF THE LAPAROSCOPIC SITES (INCISIONS). THE BLUE PLASTIC END WAS FOUND AND RETRIEVED WITHOUT SURGICAL DELAY OR PATIENT INJURY. THIS REPORT IS BEING FILED BASED ON THE POTENTIAL FOR INJURY WITH RECURRENCE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6527431 ↗MalfunctionMar 24, 2016Detachment Of Device Component
THE CUSTOMER REPORTED THAT DURING USE OF THE LAPAROSCOPIC IRRIGATION/ASPIRATION NEEDLE, 16 GA, 5MM X40CM LENGTH, IN A LAPAROSCOPIC PROCEDURE ON (B)(6) 2016, THE BLUE PLASTIC NEEDLE HOUSING DETACHED FROM THE DEVICE WHILE INSIDE THE PATIENT'S PERITONEAL CAVITY. AS REPORTED, THE DETACHED NEEDLE COMPONENT WAS RETRIEVED AND REMOVED SUCCESSFULLY FROM THE PATIENT'S PERITONEAL CAVITY. THE PROCEDURE WAS OTHERWISE COMPLETED WITH NO INJURY TO THE PATIENT. TO DATE, THERE HAS BEEN NO ADDITIONAL INFORMATION RECEIVED REGARDING THE PATIENT'S LATEST CONDITION OR ANY INDICATION THAT A LONG TERM ADVERSE EFFECT HAS OCCURRED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 5524204 ↗
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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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