ULTRAPRO UPPL2Recalls & reported problems
Johnson & Johnson International Inc. · Polypropylene partially absorbable large blue / undyed Plug and Onlay Patch · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10705031132429), received between Apr 30, 2018 and Jun 13, 2024 — classified as 3 injuries.
The most frequently reported specific device problem is “Migration” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Appropriate Device Problem Term/Code Not Available1
- Migration1
Patient problems
- Failure of Implant1
- Foreign Body In Patient1
- Hernia1
- Injury1
- Not Applicable1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryJun 13, 2024Migration; Migration
IT WAS REPORTED THAT A PATIENT UNDERWENT AN UNKNOWN PROCEDURE ON AN UNKNOWN DATE AND MESH WAS IMPLANTED. THE PATIENT REPORTED THE MESH MIGRATED INTO THE INGUINAL CANAL ALL THE WAY INTO THE SCROTUM. THE PATIENT HAD TO HAVE AN ORCHIECTOMY, WHICH HE STATES WAS HIS FOURTH SURGERY. NO FURTHER INFORMATION IS AVAILABLE AS THE REPORTER CONTACT DETAILS WERE NOT DISCLOSED.
Patient problems: Failure of Implant; Foreign Body In Patient
MAUDE report 19527749 ↗InjuryAug 13, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED BY AN ATTORNEY THAT THE PATIENT UNDERWENT BILATERAL INGUINAL HERNIA REPAIR SURGERY ON (B)(6) 2015 AND MESH WERE IMPLANTED. NO ADDITIONAL INFORMATION IS PROVIDED.
Patient problems: Injury
MAUDE report 8887248 ↗InjuryApr 30, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
IT WAS REPORTED BY AN ATTORNEY THAT THE PATIENT UNDERWENT A HERNIA REPAIR SURGERY ON (B)(6) 2010 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT SHE EXPERIENCED UNDISCLOSED INJURIES. IT WAS REPORTED BY AN ATTORNEY THAT THE PATIENT UNDERWENT A HERNIA REPAIR SURGERY ON (B)(6) 2015 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT FOLLOWING INSERTION THE PATIENT EXPERIENCED RECURRENT VENTRAL HERNIA. NO ADDITIONAL INFORMATION WAS PROVIDED.
Patient problems: Hernia; Not Applicable
MAUDE report 7474021 ↗
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- VENTRALEX 0010302Davol Inc. · Mesh, surgical, polymeric4 deaths531 reports
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- 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 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.
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