Atlas FDA

LeGoo Endovascular Occlusion Gel-0.5 mL LeGoo w/ no Cannula Product Number: PV-50 LeGoo is a water-soluble, biocompatibl

FDA device recall Z-2142-2013 · posted 2013-09-03 · Terminated

Recall details

Recalling firm
Genzyme Corporation, A Sanofi Company
Reason for recall
Product contains particulates (fibers)
Action taken
Genzyme sent a Medical Device Recall Notification letter dated June 21, 2013, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were avised to immediately discontinue use of all lots of LeGoo Endovascular Occlusion Gel and return all LeGoo and return product with the shipping label and packing slip enclosed. syringes.Complete the reply card via fax (414) 459-8791. Customer with questions were instructed to call GENCO at 877-674-2087. For questions regarding this recall call 508-270-2285.
Root cause
Material/Component Contamination
Status
Terminated
Product code
OBC
Quantity affected
5 units
Distribution
Worldwide Distribution - USA (nationwide) and internationally to Austria, Belgium, Canada, Denmark, Egypt. Europe, Finland, France, Germany, Hong Kong, Ireland, Italy, Netherlands, Poland, Saudi Arabi
Date initiated
2013-06-21
Date posted
2013-09-03
Date terminated
2014-08-07
Location
Woburn, MA

Monitor recalls programmatically

Recalls and clearances share one API, with change alerts when new recalls post.