Surgipro ll VP-585-XRecalls & reported problems
Covidien LP · Monofilament Polypropylene · Class 2 · Implant
All models of Surgipro ll (70)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884521038004), received between Apr 22, 2021 and Apr 22, 2021 — classified as 1 injury.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Abscess1
- Hemorrhage/Blood Loss/Bleeding1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 22, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ACCORDING TO THE LITERATURE SOURCE, A PROSPECTIVE STUDY COMPARED PANCREATICOGASTROSTOMY (PG) AND PANCREATICOJEJUNOSTOMY (PJ) WITH REGARD TO THE INCIDENCE OF DELAYED GASTRIC EMPTYING IN PATIENTS WHO UNDERWENT PANCREATICODUODENECTOMY BETWEEN MAY 2013 AND JANUARY 2016. THERE WERE 27 PG PATIENTS AND 26 PJ PATIENTS. THE DEVICE WAS USED FOR THE PANCREATICOGASTROSTOMY. COMPLICATIONS INCLUDED: BLOOD LOSS GREATER THAN 500ML, ABDOMINAL ABSCESS, AND INTRA-ABDOMINAL HEMORRHAGE.
Patient problems: Abscess; Hemorrhage/Blood Loss/Bleeding
MAUDE report 11706007 ↗
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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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