Wills Oglesby G09891Recalls & reported problems
Cook Incorporated · Wills-Oglesby Percutaneous Gastrostomy Catheter · Class 2 · Implant
Data updated Oct 18, 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 00827002098916), received between Jan 19, 2017 and Feb 15, 2018 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Loose or Intermittent Connection” (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 18, 2026.
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available1
- Loose or Intermittent Connection1
Patient problems
- No Code Available1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 15, 2018Loose or Intermittent Connection
THE COMPLAINANT REPORTED THAT THE CAP OF THE FEEDING ADAPTER DID NOT CLOSE WELL AND IT WAS VERY "LOOSE-FITTING". THERE WERE NO REPORTS OF ADVERSE EFFECTS TO THE PATIENT AS A RESULT OF THIS PRODUCT PROBLEM.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7273038 ↗InjuryJan 19, 2017Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
INTERNATIONAL CUSTOMER REPORTED THAT A PATIENT UNDERWENT AN UNSPECIFIED SURGICAL PROCEDURE WITH IMPLANTATION OF A WILLS-OGLESBY PERCUTANEOUS GASTROSTOMY CATHETER ON AN UNKNOWN DATE. NO PROCEDURE RELATED DETAILS WERE PROVIDED. THE PATIENT RETURNED TWO WEEKS POST PROCEDURE WITH A REPORT THAT THE DEVICE HAD A PROBLEM. EXAMINATION OF THE PATIENT AND DEVICE INDICATED THAT THE FEEDING LID WAS PUSHING BACK WHILE IN THE LOCKED POSITION. THE LID PORTION OF THE DEVICE WAS REMOVED AND REPLACED WITH A NEW LID. NO FURTHER EVENT OR PATIENT DETAILS WERE PROVIDED.
Patient problems: No Code Available
MAUDE report 6263681 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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