International safety notice
It was discovered that the label of the affected product had omitted the legally required "reuse prohibited" statement. I decided to collect it.
Japan / PMDA Recalls · JPN · May 1, 2023
Key facts
| Title | It was discovered that the label of the affected product had omitted the legally required "reuse prohibited" statement. I decided to collect it. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common Name: (1) (2) Single Use Pulse Oximeter Probe Sales name: (1) NONIN soft cloth disposable sensor (2) NONIN microform disposable sensor |
| Manufacturer | Japan Medical Next Co., Ltd. |
| Models | 569-2103, 2246-1, 7426-003, 7427-004, 2236-1, 7426-004, 2243-1 |
| Date | May 1, 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