International safety notice
Regarding the remanufactured medical device "Remanufactured Trocker E (Hogi)", the inspection record (performance test; sleeve and trotter) We have decided to voluntarily recall the car because there are some parts that are not listed in the car connection inspection) and there is no guarantee of connectivity. I did it.
Japan / PMDA Recalls · JPN · Sep 26, 2023
Key facts
| Title | Regarding the remanufactured medical device "Remanufactured Trocker E (Hogi)", the inspection record (performance test; sleeve and trotter) We have decided to voluntarily recall the car because there are some parts that are not listed in the car connection inspection) and there is no guarantee of connectivity. I did it. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common Name: Remanufactured Single Use Trocar Sleeve (Remanufactured Abdominal Trocar/Remanufactured Chest Trocar/Remanufactured Remanufactured Trocar Sleeve) Dusa) Sales name: Remanufactured Trocker E (Hogi) |
| Manufacturer | Hogy Medical Co., Ltd. |
| Models | TR002203256X, TR002204482Z, TR002203954, TR002203894, TR002203398, 3620452959, TR002203401P, CB5STR, 3120452072, TR002202723V, TR002203255W, TR002204040P |
| Date | Sep 26, 2023 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1