FDA recall notice
Infusion Pump Battery Recall: ICU Medical Removes Some CSB Batteries Intended For Use With…
FDA Recall Confirmed · Infusion Pumps · posted Dec 20, 2024
Key facts
| Notice | Infusion Pump Battery Recall: ICU Medical Removes Some CSB Batteries Intended For Use With Plum 360, A+, and A+3 Infusion Systems Due to Reports of Allegedly Counterfeit, Untested Batteries In Use |
|---|---|
| Device type | Infusion Pumps |
| Status | Recall Confirmed |
| Posted | Dec 20, 2024 |
| Notice on fda.gov | fda.gov |
At a glance
- Confirmed Recall confirmed
- Yes Currently listed by the FDA
- None Recall events referenced
- None UDI device identifiers named
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recall notices and early alerts
The FDA's Medical Device Recalls and Early Alerts list covers the most serious device recalls, plus early alerts about potentially high-risk device issues while the FDA is still collecting information. A notice is updated as the recall is confirmed or changes.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls and Early Alerts · Source date: