7 FDA recalls mention Benzonatate. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Benzonatate.
Reason Superpotent drug: Assay results were slightly above specification at the time zero point.
Reason Labeling: Label Mix-up: Bottle labeled as Benzonatate 100 mg capsules contained Benzphetamine 50 mg tablets and a bottle labeled as Benzphetamine 50…
Reason Failed Stability Specifications: Out of Specification results obtained for preservative Methylparaben content.
Reason Failed Tablet/Capsule Specifications; recall initiated by manufacturer due to reports of wet capsules
Reason Failed Tablet/Capsule Specifications: Recall due to wet and/or leaking capsules.
Reason Failed Tablet/Capsule Specifications: Recall due to wet and/or leaking capsules.
Reason Presence of Foreign Capsules/Tablets: Benzonatate 100 mg co-mingled with benzonatate 200 mg capsules.
Tell us which medications you take. If the FDA recalls one, we email you - in plain English, with what to do. Free.