SURGICEL SNoW 2092Recalls & reported problems
Ethicon, LLC · Surgicel Absorbable Hemostat, Structured Non-Woven Fabric · Class 3 · Implant
All models of SURGICEL SNoW (5)
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 10705031063624), received between Nov 14, 2024 and Nov 14, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Material Integrity Problem” (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.
Reports received per month
Most reported problems
Device problems
- Material Integrity Problem1
Patient problems
- Foreign Body In Patient1
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 14, 2024Material Integrity Problem; Material Integrity Problem
IT WAS REPORTED THAT A PATIENT UNDERWENT AN EMERGENCY LAPAROSCOPIC OVARIAN CYSTECTOMY PROCEDURE ON AN UNKNOWN DATE AND AN ABSORBABLE HEMOSTAT WAS USED. A YOUNG GIRL CAME FROM THE PROCEDURE, WHICH WENT WELL. THE ABSORBABLE HEMOSTAT WAS LAPAROSCOPICALLY PUT IN THE DEFECT WHERE THE CYST WAS, INTO THE BED OF THE OVARY. IT WASN¿T A LARGE CYST, LESS THAN 5CM. SIX MONTHS LATER SHE PRESENTED WITH PAIN AND SCAN SHOWED THAT A COMPLEX CYST HAD RE-FORMED. HOWEVER ON RE-LAPAROSCOPING HER IT WAS FOUND THAT ALL THE ABSORBABLE HEMOSTAT WAS STILL PRESENT WITHIN THE OVARY AND HAD NOT DISSOLVED AT ALL. IT HAD FORMED A DARK BROWN CRUST AND LOOKED LIKE NONE AT ALL HAD BEEN ABSORBED. IT WAS PARTICULARLY TRICKY BECAUSE IT DID NOT GO UP THE SUCTION WELL ONCE IRRIGATED, SO THE SURGEON PICKED IT ALL OUT WITH GRASPERS, WHICH TOOK A WHILE. ADDITIONAL INFORMATION WAS REQUESTED
Patient problems: Foreign Body In Patient; Pain
MAUDE report 20684888 ↗
Other Agent, absorbable hemostatic, non-collagen based devices
- ETHICON 3013SPEthicon, LLC · Agent, absorbable hemostatic, non-collagen based3 deaths392 reports
- SURGICEL FIBRILLAR 1961Ethicon Sàrl · Agent, absorbable hemostatic, non-collagen based1 recall2 deaths120 reports
- SURGICEL FIBRILLAR 1963Ethicon Sàrl · Agent, absorbable hemostatic, non-collagen based1 recall44 reports
- SURGICEL 1953Ethicon Sàrl · Agent, absorbable hemostatic, non-collagen based56 reports
- SURGICEL 1952Ethicon Sàrl · Agent, absorbable hemostatic, non-collagen based1 death41 reports
- SURGICEL FIBRILLAR 1962Ethicon Sàrl · Agent, absorbable hemostatic, non-collagen based35 reports
- Veriset HP0510ECovidien LP · Agent, Absorbable Hemostatic, Non-Collagen Based1 death33 reports
- SURGICEL SNoW 2082Ethicon, LLC · Agent, absorbable hemostatic, non-collagen based24 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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