Aidapak Services, LLC Recall: FAMOTIDINE Tablet, 20 mg, Over The Counter, Distributed by:
Aidapak Services, LLC Recall: FAMOTIDINE Tablet, 20 mg, Over The Counter, Distributed by: is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Aidapak Services, LLC; Product: FAMOTIDINE Tablet, 20 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 16714036104; Reason for recall
| Recalling firm | Aidapak Services, LLC |
|---|---|
| Product | FAMOTIDINE Tablet, 20 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 16714036104 |
| Reason for recall | Labeling: Label Mixup; FAMOTIDINE Tablet, 20 mg may be potentially mislabeled as CARVEDILOL PHOSPHATE ER, Capsule, 20 mg, NDC 00007337113, Pedigree: W003225, EXP: 6/17/2014; DULoxetine HCl DR, Capsule, 20 mg, NDC 00002323560, Pedigree: W003506, EXP: 6/21/2014; FAMOTIDINE, Tablet, 20 mg, NDC 16714036104, Pedigree: W003507, EXP: 6/21/2014; MYCOPHENOLATE MOFETIL, Capsule, 250 mg, NDC 0037822500 |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Repacked drugs were distributed in Arizona, California, Oregon, and Washington. |
| Recall initiated | 20130702 |
| Recall number | D-518-2014 |
| Category | drug |
| State | WA |
| Country | United States |
$29/mo
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