Silarx Pharmaceutical, Inc. recalls Lamivudine Oral Solution, USP, 10 mg per 1 mL, 240 mL bottle (8 ounces), Rx only, Manufactured by: Silarx Pharmaceutical
Recalled September 9, 2015 · FDA recall D-1416-2015 · Silarx Pharmaceutical
Hazard
Labeling: Incorrect or Missing Lot and/or Exp. Date - Firm received a customer complaint that the expiration date printed on the unit carton (5/18) does not match the expiration date on the bottle label (5/17). · FDA Class III
Units
576 bottles
Sold at
Nationwide
Description
Labeling: Incorrect or Missing Lot and/or Exp. Date - Firm received a customer complaint that the expiration date printed on the unit carton (5/18) does not match the expiration date on the bottle label (5/17).
Product
Lamivudine Oral Solution, USP, 10 mg per 1 mL, 240 mL bottle (8 ounces), Rx only, Manufactured by: Silarx Pharmaceuticals, Inc. Carmel, NY 10512, NDC 54838-0566-70
Manufacturer(s)
Silarx Pharmaceutical, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →