FDA Device recall Z-1177-2013
Maquet Getinge Group battery modules for use with Maquet SERVO-i ventilator systems (Part #6487180)
- FDA Device
- Class I
- terminated
- Published 2013-05-08
On 2013-05-08 the FDA classified a Class I recall of Maquet Getinge Group battery modules for use with Maquet SERVO-i ventilator systems (Part #6487180) by Maquet Cardiovascular Us Sales, citing when using the SERVO-i on battery power, in a very small number of cases, some battery modules distributed after January 31, 2010 have a shorter battery run time than expected.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1177-2013 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2013-03-07 |
| Published | 2013-05-08 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Maquet Cardiovascular Us Sales |
| Distribution | US |
Product
Maquet Getinge Group battery modules for use with Maquet SERVO-i ventilator systems (Part #6487180). Battery for use with the SERVO-i Ventilator System. The SERVO-i Ventilator System is intended for treating and monitoring patients ranging from neonates to adults with respiratory failure or insufficiency. The ventilator is equipped with at least 2, NiMH battery modules (Part No. 6487180) which automatically supply 12V DC Power in case of an AC power failure, ensuring that ventilator settings and stored data remain intact in the event of an AC power failure. The battery modules give the user a possibility to use the SERVO-i during intra-hospital transportation.
Reason
When using the SERVO-i on battery power, in a very small number of cases, some battery modules distributed after January 31, 2010 have a shorter battery run time than expected.
Identifiers
| code_info | SERVO-i Battery Module part number is 6487180. Notice pertains to Battery Modules manufactured between February 2010 a…SERVO-i Battery Module part number is 6487180. Notice pertains to Battery Modules manufactured between February 2010 and October 2012 with date codes between 1005 and 1243. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1177-2013%22
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