Codman ISOCOOL Bipolar Forceps-are indicated for cauterizing, coagulating, grasping, and manipulating tissue during general surgery, neurosurgery, ENT surgery, OB/GYN surgery, and maxillofacial / plastic surgery procedures. Model # 8145100S
FDA Recall Z-2206-2019 · Posted None
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Recalling FirmIntegra LifeSciences Corp.
Recall StatusTerminated
Product CodeGEI
Date Initiated2019-07-19
Date Terminated2020-05-22
Product Quantity125 units
Reason for Recall
Tips have an inadequate product insulation coating, which could result in the tips not coagulating as expected
Firm Action
Integra LifeSciences issued recall letter on July 19, 2019 advising of problem, health risk and action to take:
1.Review your inventory and determine if you have any impacted lot.
2. If you do have product with an affected Lot Number, stop using the product
immediately and remove the product from service.
3. Complete the attached form. If you do not have affected product, check the box, I do not have any product with the lot number.
4. If you do have affected product, check the box I do have product{s) with the lot
number. Record the total quantity of affected product you have.
5. Complete the other information and Return the completed "Acknowledgement and Return Form" by email or fax indicating your receipt and review of this notification. Keep a copy of the form for your records.
Customer Service will contact you and provide an RMA number and directions to return the product. A replacement order will also be placed for the quantity noted on the form. Customer Service Monday to Friday 8:00 AM - 8:00 PM EST
USA: 1-800-654-2873: email: [email protected] Outside USA: 781-565-1401
Root Cause
Under Investigation by firm
Distribution Pattern
KY,NJ, RI, TX, WA Foreign: BE
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.
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