ADP 3.2 Adapter, non sterile reusable Model Number: 30-801-1, an accessory used with the TissueLink Bipolar Floating Device
FDA Recall Z-1416-04 · Posted 2004-09-01
Recalling FirmTissueLink Medical, Inc.
Recall StatusTerminated
Product CodeGEI
Date Initiated2004-07-22
Date Terminated2004-10-04
Product Quantity96 units
Reason for Recall
Adapter when connected to a generator may short circuit resulting in lack of power and/or thermal warming of the ADP housing.
Firm Action
TissueLink notified the sales force on 7/22/04 to visit each account and retreive product at the hospital level.
Root Cause
Other
Distribution Pattern
Nationwide
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.