Synthetopes Inc recalls Sn-Tetrofosmin Kit 5.0 mL, Thaw and Vent before use, Not for Direct Injection, Store Frozen, Synthetopes, Inc.
Recalled June 19, 2019 · FDA recall D-1405-2019 · Synthetopes
Hazard
Lack of Processing Controls. · FDA Class II
Units
Unknown
Sold at
Nationwide.
Description
Lack of Processing Controls.
Product
Sn-Tetrofosmin Kit 5.0 mL, Thaw and Vent before use, Not for Direct Injection, Store Frozen, Synthetopes, Inc.
Manufacturer(s)
Synthetopes Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →