International safety notice
We have confirmed the shipment of products that do not comply with the maximum magnetic flux density specified by the certification standards, so we are voluntarily recalling the affected products. vinegar.
Japan / PMDA Recalls · JPN · Dec 18, 2023
Key facts
| Title | We have confirmed the shipment of products that do not comply with the maximum magnetic flux density specified by the certification standards, so we are voluntarily recalling the affected products. vinegar. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Home permanent magnet magnetic therapy device Sales name: (1) Pip Magneloop EX (2) Pip Magneloop MAX (3) Pip Magneloop |
| Manufacturer | Pip Co., Ltd. |
| Models | EB02C002, EA26B036, EA26B002, EA28B037, EB04B002, EB01B005, EB01B037, EA24B007, EB08B036, EB02B002, EA26B003, EA24B002 and 22 more |
| Date | Dec 18, 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