Drug recall D-0284-2019
Product
Nitrofurantoin Monohydrate/Macrocrystals capsules,100 mg, packaged in HDPE 60 cc bottles, Rx only, MFG: Sandoz Inc., Princeton, NJ, Repackaged by: RemedyRepack, Indiana, PA, Original NDC 00185-0122-01Repackaged NDC 70518-1087-00, 14 capsules in HDPE 60 cc bottles in cardboard trays & HDPE 60 cc bottles in plastic bags, Repackaged NDC 70518-1087-01, 10 capsules in HDPE 60 cc bottles in cardboard trays.
Reason for recall
Cross contamination with other products: Product is being recalled due to the potential presence of unrelated ingredients (Benazepril, Haloperidol and Perphenazine).
Lots and codes
Lot #: B0484872-081718, B0481339-081018, Exp 08/2019; B0506246-092718, Exp 09/2019; B0509938-100418, Exp 10/2019
Recall details
- Recalling firm
- RemedyRepack Inc., Indiana, PA
- Quantity
- 3,148 capsules
- Distribution
- Product was distributed to two medical facilities in Pennsylvania.
- Type
- Voluntary: Firm initiated
- Recall initiated
- November 7, 2018
- Terminated
- April 1, 2019
Related products
- NDC 70518-1087 Nitrofurantoin (monohydrate/macrocrystals) · Nitrofurantoin Monohydrate 75 mg/1; Nitrofurantoin 25 mg/1 · REMEDYREPACK INC.