FDA Device recall Z-0457-2026
BATTERY FLEX-3S2P 10.8V 18650 LI-ION SMBUS used with affected patient monitors Model No 2062895-001 Manufacturer Part Number U80296-1R01, r…
- FDA Device
- Class II
- ongoing
- Published 2025-11-19
On 2025-11-19 the FDA classified a Class II recall of BATTERY FLEX-3S2P 10.8V 18650 LI-ION SMBUS used with affected patient monitors Model No 2062895-001 Manufacturer Part Number U80296-1R01, r… by Ge Healthcare Finland Oy, citing potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situa….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0457-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-09-26 |
| Published | 2025-11-19 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Ge Healthcare Finland Oy |
| Distribution | US |
Product
BATTERY FLEX-3S2P 10.8V 18650 LI-ION SMBUS used with affected patient monitors Model No 2062895-001 Manufacturer Part Number U80296-1R01, revision S
Reason
Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.
Identifiers
| code_info | No UDI Manufacturing date range (YYYY-MM-DD date format, located underneath date of manufacture symbol): 2024-11-25 -…No UDI Manufacturing date range (YYYY-MM-DD date format, located underneath date of manufacture symbol): 2024-11-25 - 2025-05-31; 2025-07-07 Serial Nos. 021725-20339 021725-22682 120924-06125 120924-05011 120924-05830 120924-03583 120924-04467 120924-04447 031425-28687 120924-04436 120924-04240 021725-21549 021725-20604 5567418-SO-1-1 031425-30157 031425-28597 031425-29489 031425-28901 031425-28978 031425-28590 031425-29484 031425-29177 021725-21521 021725-20357 021725-20412 021725-22331 120924-04465 120924-07616 120924-07484 120924-07792 120924-07909 120924-07359 120924-07524 120924-06997 120924-07861 120924-08477 120924-07878 120924-07726 120924-07799 120924-08618 120924-07791 120924-08527 120924-07862 120924-08616 120924-08622 031425-29009 031425-28366 031425-30139 031425-28758 031425-29924 031425-29879 031425-28136 031425-29340 031425-29934 031425-28144 031425-28970 031425-29883 031425-28120 031425-27976 031425-29349 031425-28713 031425-28188 021725-22330 021725-21579 021725-2127 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0457-2026%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.