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The finished product labels do not declare sub-ingredients of Wheat (flour).
Presence of Particulate Matter
Lack of Assurance of Sterility: Firm mistakenly released quarantined, non conforming material that failed sterility testing.
FDA samples of product tested positive for Fumonisin
Duane Reade is recalling Pediatric Oral Electrolyte Solution because of deficient sodium and potassium content.
Lack of Assurance of Sterility; Product recalled due to displacement of the aluminum crimp cap during product usage.
Presence of Particulate Matter: This product is being recalled due to the discovery of particles in the stability samples and retain samples.
Mold in the product.
Presence of Particulate Matter: A single visible particulate was observed in a retention sample bottles identified as stainless steel
Impurities/Degradation Products: Out Of Specification levels of nitrogen dioxide.
Adulterated Presence of Foreign Tablets: Dr. Reddy's Laboratories has received complaints of mislabeled bottles of Amlodipine Besylate and Benazepril Hydrochloride Capsules and Ciprofloxacin Tablets.
Adulterated Presence of Foreign Tablets: Dr. Reddy's Laboratories has received complaints of mislabeled bottles of Amlodipine Besylate and Benazepril Hydrochloride Capsules and Ciprofloxacin Tablets
Aflatoxin test results above the established limit of 20 parts per billion
Tablet Thickness: Recall was initiated due to the presence of one slightly oversized tablet in a bottle of the identified lot.
PR State Department sampling found positive results for Clostridium Clostridioforme