Pramipexole Dihydrochloride Tablets 0.125 mg, 90 Ct Bottles recall — FDA D-0653-2016
Presence of Foreign Tablets/Capsules: Presence of a comingled Carbimazole 5 mg tablet.
Complete FDA and NHTSA recall records dated in 2016, organized for browsing by month, category and recalling company.
Select a month to review the recall records reported during that period.
Records are ordered by the best available source date.
Presence of Foreign Tablets/Capsules: Presence of a comingled Carbimazole 5 mg tablet.
Microbial Contamination of Non-Sterile Products: Syrspend SF and Syrspend SF Grape Flavor are being recalled due to the presence of yeast.
Failed Impurities/Degradation Specifications; 9 month stability timepoint
Presence of Foreign Substance: customer complaint that one unit dose cup contained a small piece of cardboard contaminant.
Microbial Contamination of Non-Sterile Products: Syrspend SF and Syrspend SF Grape Flavor are being recalled due to the presence of yeast.
Microbial Contamination of Non-Sterile Products: Syrspend SF and Syrspend SF Grape Flavor are being recalled due to the presence of yeast.
Sub-potent Drug; firm's analysis revealed subpotent result for morphine sulfate assay.
Undeclared walnuts
This Bar Saves Lives is recalling This Kid Saves Lives Chocolate Chip because the product contains whey protein and does not identify milk.
Madison One Acme, Inc. dba Solstice Medicine is recalling Tong Ren Tang Shenjing Shuairuo Wan because it contains the unapproved dietary ingredient human placenta which may transmit disease.
Dove Chocolate Assortment Snowflakes may contain undeclared peanuts, what and egg ingredients.
Undeclared walnuts
Undeclared walnuts
Signature Cafe Traditional Stuffing may have the incorrect ingredient and nutritional label that does not declare the allergens soy, milk and wheat.
Zatarain's is initiating a voluntary recall of Zatarain's Red Beans And Rice Original 8 oz. package, USPC 7142909849 with date code of BEST BY JUL 31 16Z as it may contain Creamy Parmesan…
FAILED TABLET/CAPSULE SPECIFICATIONS: Firm is recalling specific lots of pregabalin capsules due to the potential presence of deformed or damaged capsules.
FAILED TABLET/CAPSULE SPECIFICATIONS: Firm is recalling specific lots of pregabalin capsules due to the potential presence of deformed or damaged capsules.
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.