fda
2 records
FDA Drug Recall: Atovaquone Oral Suspension, USP 750 mg/5 mL, 210 mL bottle, Rx only, Distributed
2024-10-23
Class I — Microbial Contamination of a Non-sterile Product: The product was found to be contaminated with Cohnella bacteria.
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FDA Drug Recall: Clobazam Oral Suspension, 2.5 mg/mL, 120 mL bottle, Rx only, Distributed by: Bio
2019-07-31
Class II — Microbial Contamination of Non-Sterile Products: Out-of-specification results for Microbial Enumeration Tests USP <61> was observed.
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fda_adverse
4 records
FDA AE Manufacturer: Bionpharma Inc.,
Drug adverse event reporter — Product: DEXAMETHASONE
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FDA AE Manufacturer: Bionpharma, Inc.
Drug adverse event reporter — Product: MAGNESIUM CITRATE
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FDA AE Manufacturer: Bionpharma Inc
Drug adverse event reporter — Product: CEVIMELINE HYDROCHLORIDE
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