ADP 3.2 Adapter, non sterile reusable Model Number: 30-801-1, an accessory used with the TissueLink Bipolar Floating Device Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
ADP 3.2 Adapter, non sterile reusable Model Number: 30-801-1, an accessory used with the TissueLink Bipolar Floating Device
Lot Codes / Batch Numbers
Lot Numbers: TLK17300, TLB02400
Products Sold
Lot Numbers: TLK17300, TLB02400
A medical device manufacturer is recalling ADP 3.2 Adapter, non sterile reusable Model Number: 30-801-1, an accessory used with the TissueLink due to Adapter when connected to a generator may short circuit resulting in lack of power and/or thermal warming of the ADP housing.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Adapter when connected to a generator may short circuit resulting in lack of power and/or thermal warming of the ADP housing.
Recommended Action
Per FDA guidance
TissueLink notified the sales force on 7/22/04 to visit each account and retreive product at the hospital level.
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