International safety notice
Some of the screws used to secure the exterior parts of the product are screws that are not coated with a screw locking agent that is out of specification. We have decided to voluntarily recall the product because we discovered that there is a possibility that the screw may become loose or come off.
Japan / PMDA Recalls · JPN · Apr 10, 2023
Key facts
| Title | Some of the screws used to secure the exterior parts of the product are screws that are not coated with a screw locking agent that is out of specification. We have decided to voluntarily recall the product because we discovered that there is a possibility that the screw may become loose or come off. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: glucose analyzer Brand name: Glutest Mint II |
| Manufacturer | PHC Corporation |
| Models | 2210419, 2200056, 2210300, 2200688, 2200046, 2210539, 2200047, 2210793, 2210600, 2190445, 2210672, 2200815 and 68 more |
| Date | Apr 10, 2023 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 1–9 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