FLUVASTATIN, Capsule, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00378802077.
Check against the official notice below — it lists the full affected range.
AidaPak Services, LLC recalled 90 capsules of Fluvastatin 20 mg because the medication may have been mislabeled as Acetaminophen/Butalbital/Caffeine tablets (325 mg/50 mg/40 mg). The affected product has pedigree number 00378802077 and expiration date W002655. The mislabeled repacked drugs were distributed in Arizona, California, Oregon, and Washington.
The recall notice does not specify what affected consumers should do.
Written by software from the official notice below. Not reviewed by a lawyer.
Labeling: Label Mixup: FLUVASTATIN, Capsule, 20 mg may have potentially been mislabeled as the following drug: ACETAMINOPHEN/ BUTALBITAL/ CAFFEINE, Tablet, 325 mg/50 mg/40 mg, NDC 00603254421, Pedigree: W002654, EXP: 6/4/2014.
Reason for recall: Labeling: Label Mixup: FLUVASTATIN, Capsule, 20 mg may have potentially been mislabeled as the following drug: ACETAMINOPHEN/ BUTALBITAL/ CAFFEINE, Tablet, 325 mg/50 mg/40 mg, NDC 00603254421, Pedigree: W002654, EXP: 6/4/2014. Distribution: Repacked drugs were distributed in Arizona, California, Oregon, and Washington. Quantity: 90 Capsules Lot/code info: FLUVASTATIN, Capsule, 20 mg has the following codes: Pedigree: 00378802077, EXP: W002655.
Official record: FDA (Drug enforcement) ↗
Republished from the official source above; details can change — the source record controls.