Conmed Corporation 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 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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
Brand
Conmed Corporation
Lot Codes / Batch Numbers
Cat No 1690-001: 0306092, 0306201, 0306202. Cat No 1690-003: 0305231, 0305232, 0306201. Cat No 1690-005: 0305162, 0305221, 0305301, 0306031, 0306042, 0306051, 0306191, 0306252, 0306301. Cat No 1690-010: 0305231, 0306171. Cat No 1690-030: 0305281, 0306031, 0306051, 0306101, 0306131, 0306161, 0306231, 0306232, 0306261
Products Sold
Cat No 1690-001: 0306092, 0306201, 0306202. Cat No 1690-003: 0305231, 0305232, 0306201. Cat No 1690-005: 0305162, 0305221, 0305301, 0306031, 0306042, 0306051, 0306191, 0306252, 0306301. Cat No 1690-010: 0305231, 0306171. Cat No 1690-030: 0305281, 0306031, 0306051, 0306101, 0306131, 0306161, 0306231, 0306232, 0306261
Conmed Corporation is recalling 1690 Ultratrace Series ECG Electrodes, clear tape ECG electrode with wet gel. This is a single use, due to Separation of the sensing element from the body of the electrode.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Separation of the sensing element from the body of the electrode.
Recommended Action
Per FDA guidance
Letters dated 7/30/03 requesting return of recalled lots and subrecall by distributors.
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 noticeDistribution
As reported by FDA
IN
Page updated: Jan 10, 2026