Conmed Electrosurgery Conmed System 5000 Electrosurgical unit, REF 60-8005-SYS, 60-8015-SYS, 60-8018-SYS, 60-8005-001, 60-8005-003, Conmed Corporation. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Conmed System 5000 Electrosurgical unit, REF 60-8005-SYS, 60-8015-SYS, 60-8018-SYS, 60-8005-001, 60-8005-003, Conmed Corporation.
Brand
Conmed Electrosurgery
Lot Codes / Batch Numbers
Serial Numbers: 06GGP 004, 06GGP 005, 06GGP 009, 06GGP 011, 06GGP 012, 06GGP 024, 06GGP 027 thru 030, 06GGP 057 thru 059, 06GGP 090 thru 092, 06GGP 131 thru 140, 06GGP 141 thru 144, 06FGP 022, 06FGP 023, 06FGP 029 thru 046, 06FGP 048 thru 056, 06FGP 062 thru 071, 06FGP 073 thru 079, 06FGP 090, 06FGP 106, 06FGP 107, 06FGP 110 thru 112 .
Products Sold
Serial Numbers: 06GGP 004, 06GGP 005, 06GGP 009, 06GGP 011, 06GGP 012, 06GGP 024, 06GGP 027 thru 030, 06GGP 057 thru 059, 06GGP 090 thru 092, 06GGP 131 thru 140, 06GGP 141 thru 144 ,,, 06FGP 022, 06FGP 023, 06FGP 029 thru 046, 06FGP 048 thru 056, 06FGP 062 thru 071, 06FGP 073 thru 079, 06FGP 090, 06FGP 106, 06FGP 107, 06FGP 110 thru 112 .
Conmed Electrosurgery is recalling Conmed System 5000 Electrosurgical unit, REF 60-8005-SYS, 60-8015-SYS, 60-8018-SYS, 60-8005-001, due to Wrong size capacitor installed in electrosurgical generator could malfunction, causing muscle stimulation or delay in therapy.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Wrong size capacitor installed in electrosurgical generator could malfunction, causing muscle stimulation or delay in therapy.
Recommended Action
Per FDA guidance
Domestic customers were notified by letter on 09/01/2006 and international accounts were notified by letter on 09/07/2006.
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