Pfizer Quillivant XR (methylphenidate HCl) for extended-release oral suspension, 900 mg/180 recall — FDA D-0609-2017
Failed Dissolution Specifications: Dissolution at 8 hour was out of specification at 12 month at 25 degree Celsius.
Complete FDA and NHTSA recall records dated in 2017, 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.
Failed Dissolution Specifications: Dissolution at 8 hour was out of specification at 12 month at 25 degree Celsius.
Failed Dissolution Specifications: Dissolution at 8 hour was out of specification at 12 month at 25 degree Celsius.
Labeling: Incorrect/Undeclared Excipients: Firm is recalling A+D Diaper Rash Cream due to a labeling claim issue.
Labeling: Label Mixup; Unit boxes labeled as Desonide Ointment 0.05% may contain tubes of Desonide Ointment labeled as Ketoconazole Cream
Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of atenolol 50 mg Tablets USP contained a paroxetine 20 mg tablet.
Failed Dissolution Specifications: Dissolution at 8 hour was out of specification at 12 month at 25 degree Celsius.
This recall has been initiated due to missing information about the presence of the milk allergen in the list of ingredients. It is written that the products contain butter, but the food…
This recall has been initiated due to missing information about the presence of the milk allergen in the list of ingredients. It is written that the products contain butter, but the food…
Product samples tested positive for lead. Finished curry products tested and ground turmeric ingredient used to manufacture the curry seasoning also tested positive for lead.
The cookie dough used in select ice creams may be contaminated with Listeria monocytogenes.
Undeclared Milk: Milk (small label 3oz and 4oz and large label 4oz) Undeclared food color: Red #40 (small label 3oz and 4oz)
Product may contain foreign matter, metal pieces.
Presence of Ephedrae Herba (ma huang), a FDA Banned Ephedra Alkaloid
Ground Turmeric may contain excess levels of lead.
Bee International is recalling Plastic Heart Tubes with Chocolate Lentils because they may contain undeclared milk protein.
Undeclared food color: Yellow #5, Yellow #5 lake, and Yellow #6 and Yellow #6 lake
This recall has been initiated due to missing information about the presence of the milk allergen in the list of ingredients. It is written that the products contain butter, but the food…
Product may contain foreign matter, metal pieces.
Product samples tested positive for lead. Finished curry products tested and ground turmeric ingredient used to manufacture the curry seasoning also tested positive for lead.
The cookie dough used in select ice creams may be contaminated with Listeria monocytogenes.
Product samples tested positive for lead. Finished curry products tested and ground turmeric ingredient used to manufacture the curry seasoning also tested positive for lead.
The allergens such as soy, milk, almond, coconut, hazelnut, and/or wheat are declared on an insert label inside of the assorted boxes, and not declared on the exterior of the boxes.
The cookie dough used in select ice creams may be contaminated with Listeria monocytogenes.
This recall has been initiated due to missing information about the presence of the milk allergen in the list of ingredients. It is written that the products contain butter, but the food…
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.