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Prescription drugs recalled for contamination, potency or labelling.
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2,003 recalls · newest first
CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B.
Labeling Incorrect Instructions: This recall has been initiated because the Instructions for Use included in the Epi-Safe Kits for the Epi-Safe…
Labeling Incorrect Instructions: This recall has been initiated because the Instructions for Use included in the Epi-Safe Kits for the Epi-Safe…
Labeling Incorrect Instructions: This recall has been initiated because the Instructions for Use included in the Epi-Safe Kits for the Epi-Safe…
Labeling Incorrect Instructions: This recall has been initiated because the Instructions for Use included in the Epi-Safe Kits for the Epi-Safe…
Failed Impurities/Degradation Specifications: unknown impurity higher than the specified limit was detected during routine stability testing.
Failed Impurities/Degradation Specifications: unknown impurity higher than the specified limit was detected during routine stability testing.
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
CGMP Deviations: products manufactured under conditions that could impact its product quality.
CGMP Deviations: products manufactured under conditions that could impact its product quality.
CGMP Deviations: products manufactured under conditions that could impact its product quality.
Microbial contamination
Microbial contamination
Microbial contamination
Microbial contamination
Microbial contamination
Microbial contamination
Microbial contamination
Microbial contamination
Microbial contamination