Cook G07090Recalls & reported problems
Cook Incorporated · Thal-Quick Chest Tube Tray · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00827002070905), received between Sep 23, 2022 and Jan 20, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Device Contaminated During Manufacture or Shipping” (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
- Device Contaminated During Manufacture or Shipping1
- Problem with Sterilization1
- Unsealed Device Packaging1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 20, 2025Device Contaminated During Manufacture or Shipping; Device Contaminated During Manufacture or Shipping
THIS REPORT IS NO LONGER MEETS THE DEFINITION OF A REPORTABLE EVENT. PLEASE SEE H11.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21193241 ↗MalfunctionSep 23, 2022Unsealed Device Packaging; Problem with Sterilization; Unsealed Device Packaging; Problem with Sterilization
ADDITIONAL INFORMATION WAS RECEIVED ON 27SEP2022 IN REGARDS TO DATE OF EVENT AND RETURN OF DEVICES. THE DATE OF EVENT OCCURRED ON 12SEP2022. RETURNING OF THE REPORTED TWO DEVICES WAS CONFIRMED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15473592 ↗
Other CATHETER, IRRIGATION devices
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- Navarre NNU8LPTBard Access Systems, Inc. · CATHETER, IRRIGATION736 reports
- BLAKE 2227Ethicon Inc. · CATHETER, IRRIGATION331 reports
- Navarre NNU6LPTBard Access Systems, Inc. · CATHETER, IRRIGATION211 reports
- Navarre Opti-Drain NOD10LPTBard Access Systems, Inc. · CATHETER, IRRIGATION178 reports
- Navarre NNU10LPTBard Access Systems, Inc. · CATHETER, IRRIGATION127 reports
- BLAKE 2233Ethicon Inc. · CATHETER, IRRIGATION114 reports
- Vasoshield VH-5001Maquet Cardiovascular LLC · Catheter, Irrigation1 recall27 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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