Cook G02791Recalls & reported problems
Cook Incorporated · Vinyl Connecting Tube · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00827002027916), received between Feb 14, 2018 and Dec 6, 2019 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Device Contaminated During Manufacture or Shipping” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Recalls naming this device
- Aug 16, 2022Class IIOpen, Classified
Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.
Z-1844-2022 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported problems
Device problems
- Device Contaminated During Manufacture or Shipping1
- Device Contamination with Chemical or Other Material1
Patient problems
- No Patient Involvement2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 6, 2019Device Contaminated During Manufacture or Shipping; Device Contaminated During Manufacture or Shipping
NO ADDITIONAL INFORMATION REGARDING THE PATIENT AND/OR EVENT HAS BEEN RECEIVED SINCE THE PREVIOUS MEDWATCH REPORT WAS SENT.
Patient problems: No Patient Involvement
MAUDE report 9432662 ↗MalfunctionFeb 14, 2018Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
THE CUSTOMER REPORTED THAT, DURING AN INSPECTION OF AN UNOPENED DRAINAGE BAG CONNECTOR CONNECTING TUBE, A STRAIN OF HAIR WAS SEEN IN THE PACKAGE. THE ISSUE WAS DISCOVERED PRIOR TO USE ON A PATIENT; ACCORDINGLY, NO PATIENT ADVERSE EVENTS OCCURRED AS A RESULT OF THE ISSUE. THE DEVICE IS REPORTEDLY AVAILABLE FOR RETURN; HOWEVER AS OF THE DATE OF THIS REPORT, NO DEVICE HAS YET BEEN RECEIVED FOR EVALUATION.
Patient problems: No Patient Involvement
MAUDE report 7272066 ↗
Other CONNECTOR, CATHETER devices
- Cook G02278Cook Incorporated · CONNECTOR, CATHETER1 recall7 reports
- Medline DYND12200Medline Industries, Inc. · CONNECTOR, CATHETER1 recall2 reports
- Cook G02327Cook Incorporated · CONNECTOR, CATHETER1 recall1 report
- Cook G02898Cook Incorporated · CONNECTOR, CATHETER1 recall0 reports
- Cook G02464Cook Incorporated · CONNECTOR, CATHETER1 recall0 reports
- CARDINAL HEALTH SU130-4601Cardinal Health 200, LLC · CONNECTOR, CATHETER1 recall0 reports
- Medline DYND2219Medline Industries, Inc. · CONNECTOR, CATHETER1 report
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 · each recall links to the FDA recall notice
- 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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