Access CardioSystems Recalls

FDA
2
Total Recalls
1
Agencies
Jul 2004
First Recall
Apr 2006
Latest Recall

Showing 1-2 of 2 recalls

FDA

AccessAED (without audio record) Model Number: 9100-0100-0

Device may fail to deliver shock due to a faulty circuit board

AccessCardiosystems issued recall letters on 11/3/04 to US Customers by Registered, Certified, Return Receipt requested USPS mail. The foreign mailings made through Federal Express with delivery confirmation.

FDA

Access AED and Access ALS Automated External Defibrillators Model No. : 9100-0100

Difibrillator may fail to operate due to a faulty component on the circuit board

Access CardioSystems notified Distributors by telephone and email on 12/18/03 and 12/19/03. Recall letters were dated 12/19/03 and issued by US Mail. Distributors are requested to locate and return AED's .