MESH, SURGICAL, POLYMERIC
This device is manufactured by ETHICON.
The following problems were reported about this device:
| Year | Description | Events/year | Type |
|---|---|---|---|
| 2024 | Weight Changes | 7 | Patient |
| 2024 | Vomiting | 10 | Patient |
| 2024 | Unspecified Tissue Injury | 2 | Patient |
| 2024 | Unspecified Infection | 8 | Patient |
| 2024 | Tachycardia | 1 | Patient |
| 2024 | Swelling/ Edema | 6 | Patient |
| 2024 | Seroma | 4 | Patient |
| 2024 | Scar Tissue | 4 | Patient |
| 2024 | Post Operative Wound Infection | 5 | Patient |
| 2024 | Perforation | 3 | Patient |
| 2024 | Pain | 28 | Patient |
| 2024 | Obstruction/Occlusion | 10 | Patient |
| 2024 | Necrosis | 3 | Patient |
| 2024 | Nausea | 10 | Patient |
| 2024 | Insufficient Information | 16 | Patient |
| 2024 | Inflammation | 17 | Patient |
| 2024 | High Blood Pressure/ Hypertension | 8 | Patient |
| 2024 | Hernia | 45 | Patient |
| 2024 | Hemorrhage/Blood Loss/Bleeding | 1 | Patient |
| 2024 | Fistula | 1 | Patient |
| 2024 | Fibrosis | 1 | Patient |
| 2024 | Erythema | 1 | Patient |
| 2024 | Discomfort | 2 | Patient |
| 2024 | Diarrhea | 3 | Patient |
| 2024 | Deformity/ Disfigurement | 1 | Patient |
| 2024 | Decreased Appetite | 4 | Patient |
| 2024 | Cramp(s) /Muscle Spasm(s) | 1 | Patient |
| 2024 | Constipation | 1 | Patient |
| 2024 | Chills | 3 | Patient |
| 2024 | Cellulitis | 3 | Patient |
| 2024 | Appropriate Term / Code Not Available | 16 | Patient |
| 2024 | Adhesion(s) | 37 | Patient |
| 2024 | Abscess | 6 | Patient |
| 2024 | Abdominal Pain | 21 | Patient |
| 2024 | Abdominal Distention | 2 | Patient |
| 2024 | Difficult to Open or Remove Packaging Material | 1 | Device |
| 2024 | Delivered as Unsterile Product | 1 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 79 | Device |
| 2023 | Pain | 1 | Patient |
| 2023 | Inflammation | 1 | Patient |
| 2023 | Hernia | 1 | Patient |
| 2023 | Adhesion(s) | 1 | Patient |
| 2023 | Abscess | 1 | Patient |
| 2023 | Adverse Event Without Identified Device or Use Problem | 1 | Device |
| 2022 | Vomiting | 1 | Patient |
| 2022 | Numbness | 1 | Patient |
| 2022 | Nausea | 1 | Patient |
| 2022 | Fatigue | 1 | Patient |
| 2022 | Constipation | 1 | Patient |
| 2022 | Appropriate Term / Code Not Available | 1 | Patient |
| 2022 | Abdominal Distention | 1 | Patient |
| 2022 | Migration | 2 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 69 | Device |
| 2020 | Adverse Event Without Identified Device or Use Problem | 2 | Device |
| 2019 | Vomiting | 1 | Patient |
| 2019 | Unspecified Infection | 1 | Patient |
| 2019 | Perforation | 1 | Patient |
| 2019 | Obstruction/Occlusion | 2 | Patient |
| 2019 | Hernia | 5 | Patient |
| 2019 | Discomfort | 1 | Patient |
| 2019 | Adhesion(s) | 1 | Patient |
| 2019 | Abdominal Pain | 1 | Patient |
| 2019 | Abdominal Distention | 1 | Patient |
| 2019 | Peeled/Delaminated | 3 | Device |
| 2019 | Packaging Problem | 1 | Device |
| 2019 | Material Split, Cut or Torn | 2 | Device |
| 2019 | Material Separation | 1 | Device |
| 2019 | Material Frayed | 1 | Device |
| 2019 | Appropriate Term/Code Not Available | 15 | Device |
| 2019 | Adverse Event Without Identified Device or Use Problem | 377 | Device |
| 2018 | Vomiting | 1 | Patient |
| 2018 | Unspecified Infection | 1 | Patient |
| 2018 | Swelling/ Edema | 1 | Patient |
| 2018 | Obstruction/Occlusion | 4 | Patient |
| 2018 | Nausea | 1 | Patient |
| 2018 | Hernia | 2 | Patient |
| 2018 | Hemorrhage/Blood Loss/Bleeding | 1 | Patient |
| 2018 | Appropriate Term / Code Not Available | 1 | Patient |
| 2018 | Adhesion(s) | 2 | Patient |
| 2018 | Abdominal Pain | 4 | Patient |
| 2018 | Tear, Rip or Hole in Device Packaging | 4 | Device |
| 2018 | Patient-Device Incompatibility | 4 | Device |
| 2018 | Migration | 1 | Device |
| 2018 | Material Split, Cut or Torn | 5 | Device |
| 2018 | Material Separation | 3 | Device |
| 2018 | Material Frayed | 1 | Device |
| 2018 | Hole In Material | 1 | Device |
| 2018 | Device Appears to Trigger Rejection | 1 | Device |
| 2018 | Break | 1 | Device |
| 2018 | Appropriate Term/Code Not Available | 44 | Device |
| 2018 | Adverse Event Without Identified Device or Use Problem | 89 | Device |
| 2017 | Migration or Expulsion of Device | 1 | Device |
| 2017 | Migration | 1 | Device |
| 2017 | Material Separation | 2 | Device |
| 2017 | Delamination | 1 | Device |
| 2017 | Appropriate Term/Code Not Available | 2 | Device |
| 2016 | Malposition of Device | 1 | Device |
| 2007 | Adverse Event Without Identified Device or Use Problem | 1 | Device |