International safety notice
When a medical institution conducted a "battery inspection" on this product, it was found that the "battery has deteriorated. We have received reports that the message "Please replace" is displayed. As a result of the investigation, it was found that changing the battery may cause the capacity to be incorrectly recognized under certain usage conditions. Therefore, we are conducting a voluntary recall to replace the batteries with ones that do not cause misidentification of capacity.
Japan / PMDA Recalls · JPN · Apr 9, 2021
Key facts
| Title | When a medical institution conducted a "battery inspection" on this product, it was found that the "battery has deteriorated. We have received reports that the message "Please replace" is displayed. As a result of the investigation, it was found that changing the battery may cause the capacity to be incorrectly recognized under certain usage conditions. Therefore, we are conducting a voluntary recall to replace the batteries with ones that do not cause misidentification of capacity. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Syringe infusion pump Brand name: (1) JMS syringe pump SP-520 (2) JMS syringe pump SP-120 |
| Manufacturer | JMS Co., Ltd. |
| Models | 20041632, 19A3811B, 19E4061B, 18G2959B, 17K0496P, 20051757, 18E2776B, 18A2534B, 15120334, 18L3381B, 16J0338P, 17K0508P and 2782 more |
| Date | Apr 9, 2021 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 1–9 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