Cardiac Science Corporation 9051 Electrode Adapter; Automated external defibrillator, Used with QUIK-COMBO System; Cardiac Science Corp, Bothell, WA 98021. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
9051 Electrode Adapter; Automated external defibrillator, Used with QUIK-COMBO System; Cardiac Science Corp, Bothell, WA 98021.
Brand
Cardiac Science Corporation
Lot Codes / Batch Numbers
Lot Numbers: W029275 and W029476.
Products Sold
Lot Numbers: W029275 and W029476.
Cardiac Science Corporation is recalling 9051 Electrode Adapter; Automated external defibrillator, Used with QUIK-COMBO System; Cardiac Scien due to Adaptor Cable Incorrectly Manufactured: The red and white connector ends of the adapter are switched. Therefore, the cable will not connect to the el. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Adaptor Cable Incorrectly Manufactured: The red and white connector ends of the adapter are switched. Therefore, the cable will not connect to the electrodes as indicated in the instructions.
Recommended Action
Per FDA guidance
Consignees were notified by an Urgent Medical Device Recall letter sent on 01/23/2008. The letter instructs users to check each cable of the affected lot to ensure that it properly connects to the electrode. Users were also instructed to return any defective product to the recalling firm for a replacement. For additional information, contact 1-888-466-8686 x2041.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026