AED Manufacturer Recalls 5,000+ Battery Packs

Published: June 14, 2010

GUILFORD, Conn.—Defibtech LLC, an automated external defibrillator (AED) manufacturer, has recalled more than 5,000 DBP-2800 battery packs used in Lifeline AEDs and ReviveR AEDs.

When the AED is used with an affected battery pack, the AED may falsely detect an error condition during charging for a shock, then cancel charge and not provide therapy, according to the company. If this situation occurs, the AED will speak “shock canceled” followed by “service code 1003” while powering off.

The recall affects 5,418 DBP-2800 battery packs shipped before June 4, 2007. The company has identified recommendations for end users to follow until the battery pack has been corrected. The recommendations are being mailed to all affected customers

For additional information, click here.

——Article Continues Below——

Get the latest industry news and research delivered directly to your inbox.

 

Posted in: News

Tagged with: AEDs

ADVERTISEMENT
ADVERTISEMENT
Strategy & Planning Series
Strategy & Planning Series
Strategy & Planning Series
Strategy & Planning Series
Strategy & Planning Series