FDA Recall Terminated

1690 Ultratrace Series ECG Electrodes, clear tape ECG electrode with wet gel. This is a single use, disposable device. Electrodes are packaged and sold as: Cat No 1690-001 (1 unit per pouch/30 per box); 1690-003 (3 units per pouch/30 per box); 1690-005 (5 units per pouch/50 per box); 1690-010 (50 units per pouch/no box/ 1000 per case); 1690-030 (30 units per pouch/no box). The above are sold in boxes of 600 with the exception of 1690-010 (sold 1000 per case) as noted above. Responsible firm on the label: Conmed Corp., 310 Broad St., Utica, New York

Recall: Z-1185-03 · Initiated July 30, 2003

Recall

Recall Number
Z-1185-03
Event Number
26988
Firm
Conmed Corporation
FEI Number
3001451571
Product Code
DRX
Status
Terminated
Root Cause
Other
Initiated
July 30, 2003
Posted
August 27, 2003
Terminated
March 21, 2005
Address
525 French Road, Utica, NY, 13502

Description

1690 Ultratrace Series ECG Electrodes, clear tape ECG electrode with wet gel. This is a single use, disposable device. Electrodes are packaged and sold as: Cat No 1690-001 (1 unit per pouch/30 per box); 1690-003 (3 units per pouch/30 per box); 1690-005 (5 units per pouch/50 per box); 1690-010 (50 units per pouch/no box/ 1000 per case); 1690-030 (30 units per pouch/no box). The above are sold in boxes of 600 with the exception of 1690-010 (sold 1000 per case) as noted above. Responsible firm on the label: Conmed Corp., 310 Broad St., Utica, New York

Reason

Separation of the sensing element from the body of the electrode.

Action

Letters dated 7/30/03 requesting return of recalled lots and subrecall by distributors.

Distribution

241 direct accounts including wholesalers and medical facilities. Of these, there are 15 foreign consignees in Canada, Belgium, Germany, Norway, The Netherlands, Spain, United Kingdom, Japan, Malaysia, Thailand, and United Arab Emirates .

Quantity

774,400 electrodes (# corrected 9/5/03)