Symbotex SYM1710EFRecalls & reported problems
Sofradim Production · Composite Mesh,Monofilament Polyester with Absorbable Collagen Film, Pre-Placed Sutures and Marking · Class 2 · Implant
All models of Symbotex (31)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10884521190429), received between Feb 24, 2021 and Feb 24, 2021 — classified as 2 injuries.
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.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem2
Patient problems
- Unspecified Infection2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryFeb 24, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ACCORDING TO THE REPORTER, THE PATIENT WAS SUSPECTED TO HAVE AN INFECTION AFTER HERNIA PROCEDURE. REOPERATION WAS DONE AND THERE WAS INTERVENTION FOR AN EXPLORATORY COELIOSCOPY FOR VERIFICATION OF THE DRAIN BECAUSE EFFUSION (ASCITE) APPEARED AND RADIO CONTROL (PELVIC ABDOMINO ULTRASOUND) TO CHECK PORTAL THROMBOSIS.
Patient problems: Unspecified Infection
MAUDE report 11372667 ↗InjuryFeb 24, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ACCORDING TO THE REPORTER, THE PATIENT WAS SUSPECTED TO HAVE AN INFECTION AFTER HERNIA PROCEDURE. REOPERATION WAS DONE AND THERE WAS INTERVENTION FOR AN EXPLORATORY COELIOSCOPY FOR VERIFICATION OF THE DRAIN BECAUSE EFFUSION (ASCITE) APPEARED AND RADIO CONTROL (PELVIC ABDOMINO ULTRASOUND) TO CHECK PORTAL THROMBOSIS.
Patient problems: Unspecified Infection
MAUDE report 11372638 ↗
Other Mesh, surgical, polymeric devices
- PROCEED PVPMJohnson & Johnson International Inc. · Mesh, surgical, polymeric1,233 reports
- PROCEED PCDN1Johnson & Johnson International Inc. · Mesh, surgical, polymeric744 reports
- PROCEED PCDG1Johnson & Johnson International Inc. · Mesh, surgical, polymeric1 recall1 death637 reports
- PROCEED PVPSJohnson & Johnson International Inc. · Mesh, surgical, polymeric622 reports
- ProGrip LPG1510Sofradim Production · Mesh, surgical, polymeric2 deaths616 reports
- VENTRALEX 0010302Davol Inc. · Mesh, surgical, polymeric4 deaths531 reports
- BARD 0112680Davol Inc. · Mesh, surgical, polymeric1 death494 reports
- ProGrip TEM1509GSofradim Production · Mesh, surgical, polymeric3 deaths471 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 16, 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