Argyle 8888750018Recalls & reported problems
Cardinal Health, Inc. · Edlich Gastric Lavage Tray,Large · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10884521000711), received between Mar 13, 2017 and Apr 15, 2022 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Complete Blockage” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Complete Blockage2
- Decrease in Suction2
- Kinked1
Patient problems
- Abdominal Distention2
- No Clinical Signs, Symptoms or Conditions1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 15, 2022Complete Blockage; Decrease in Suction; Complete Blockage; Decrease in Suction
CUSTOMER REPORTS: THERE IS AN ISSUE WITH THE REPLOGLE SUCTION CATHETER. THE NURSING STAFF TRIED ONE THIS MORNING AND IT WAS DEFECTIVE. ADDITIONAL INFORMATION WAS RECEIVED ON 4/14/22 STATING THAT THE REPLOGLE WAS FOUND OCCLUDED; IT WOULD NOT ASPIRATE OR FLUSH WITH AIR. THE DEVICE WAS REPLACED AND NO FURTHER MEDICAL INTERVENTION WAS REQUIRED.
Patient problems: Abdominal Distention
MAUDE report 14118515 ↗MalfunctionMar 29, 2022Complete Blockage; Decrease in Suction; Complete Blockage; Decrease in Suction
CUSTOMER REPORTS: THERE IS AN ISSUE WITH THE REPLOGLE SUCTION CATHETER. THE REPLOGLE WAS IN PLACE AT THE START OF THE RN'S SHIFT AND WAS FOUND OCCLUDED; IT WOULD NOT ASPIRATE OR FLUSH WITH AIR.
Patient problems: Abdominal Distention; No Clinical Signs, Symptoms or Conditions
MAUDE report 13938962 ↗MalfunctionMar 13, 2017Kinked
IT WAS REPORTED TO COVIDIEN ON (B)(6) 2016 THAT A CUSTOMER HAD AN ISSUE WITH A GASTRO INTESTINAL TUBE. THE CUSTOMER REPORTED THAT UPON OPENING THE PACKAGE THE TUBING WAS BADLY KINKED. IT WAS TO THE POINT WHERE IT COULD NOT BE USED. THIS IS THE THIRD OCCURRENCE IN THE SAME ITEM/DIFFERENT LOT NUMBERS THAT THIS CUSTOMER HAS ENCOUNTERED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6401088 ↗
Other CATHETER (GASTRIC, COLONIC, ETC.), IRRIGATION AND ASPIRATION devices
- Argyle 8886864604Cardinal Health, Inc. · CATHETER (GASTRIC, COLONIC, ETC.), IRRIGATION AND ASPIRATION2 reports
- Aspiration Catheter 92796Avanos Medical, Inc. · CATHETER (GASTRIC, COLONIC, ETC.), IRRIGATION AND ASPIRATION1 report
- Halyard 92774Avanos Medical, Inc. · CATHETER (GASTRIC, COLONIC, ETC.), IRRIGATION AND ASPIRATION1 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 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.
How reports and recalls are matched · Editorial policy · Report an error on this page