Biocompatibles U.K., Ltd. recalls Varithena (polidocanol injectable foam) Administration Pack For Use With Varithena, Rx only, Distributed by Biocompatibl
Recalled October 12, 2016 · FDA recall D-0001-2017 · Biocompatibles U.K
Hazard
Defective Delivery System: Incorrect type of syringe found in commercially distributed administration pack · FDA Class III
Units
3,254 administration packs
Sold at
Distributed nationwide
Description
Defective Delivery System: Incorrect type of syringe found in commercially distributed administration pack
Product
Varithena (polidocanol injectable foam) Administration Pack For Use With Varithena, Rx only, Distributed by Biocompatibles, Inc. Oxford, CT 06478, NDC 60635-123-01
Manufacturer(s)
Biocompatibles U.K., Ltd.
Made in
United Kingdom
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →