International safety notice
Products subject to recall are those whose main assembly facility (overseas manufacturer) is the foreign manufacturer. Since it was manufactured before registration and was manufactured by an unregistered manufacturing facility, we will collect it.
Japan / PMDA Recalls · JPN · Nov 30, 2022
Key facts
| Title | Products subject to recall are those whose main assembly facility (overseas manufacturer) is the foreign manufacturer. Since it was manufactured before registration and was manufactured by an unregistered manufacturing facility, we will collect it. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Dental occlusal splint material Sales name: (1) Temp Basic Transpa (2) Terapon Transpa ST |
| Manufacturer | Toshin Dental Co., Ltd. |
| Models | 95H16／11773, 15603, 95H12／11236, 13213, 95H20／13113, 14309, 95H16／13082, 15392, 15507, 13085, 95H20／11547, 95H25／12178 |
| Date | Nov 30, 2022 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 Matching catalog numbers in FDA data
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