Synthetopes Inc recalls Pentreotide (10 uGm), Not for Direct Injection, Synthetopes, Inc.
Recalled June 19, 2019 · FDA recall D-1399-2019 · Synthetopes
Hazard
Lack of Processing Controls. · FDA Class II
Units
20 vials
Sold at
Nationwide.
Description
Lack of Processing Controls.
Product
Pentreotide (10 uGm), Not for Direct Injection, Synthetopes, Inc.
Manufacturer(s)
Synthetopes Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →