Cook G07467Recalls & reported problems
Cook Incorporated · Thal-Quick Chest Tube Fitting · Class 1
Data updated Oct 13, 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 00827002074675), received between Nov 9, 2017 and Nov 9, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fluid/Blood Leak” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Fluid/Blood Leak1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 9, 2017Fluid/Blood Leak; Fluid/Blood Leak
THE CUSTOMER REPORTED THAT THE THAL-QUICK CHEST TUBE ADAPTER LEAKED "AT THE LEVEL OF THE STOPCOCK UNDER THE INJECTION SITE" (SIC). THE CHEST TUBE SET ITSELF WAS PLACED IN AUXILIARY ACCESS FOR PLEURAL FLUID DRAINAGE. THE OPERATOR WAS ATTEMPTING TO ADMINISTER UROKINASE/NACL AND THEN PULMOZYME/NACL. THE INJECTION WAS ULTIMATELY PERFORMED BY TAKING OFF THE CAP ON THE STOPCOCK AND PLACING A CAP ON THE 1ST INJECTION SITE, WHICH DID NOT LEAK. ADDITIONALLY, THE CUSTOMER REPORTED THAT THE INSTRUCTION FOR USE (IFU) WERE NOT SHIPPED WITH THE DEVICE, SO THE OPERATOR WAS NOT SURE IF THE DEVICE WAS SUITABLE FOR INJECTION OR NOT. THE CLINICAL CONSEQUENCES WHICH RESULTED FROM THE PRODUCT ISSUE WERE REPORTED TO BE A LOSS OF THE PATIENT'S MEDICINE AS WELL AS A DELAY OF THE INTENDED INJECTION. THE PRODUCT IS REPORTEDLY UNAVAILABLE FOR EVALUATION.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7015400 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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