162 FDA recalls mention Star. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Star.
Reason Failed Tablet/Capsule Specifications: Complaints of empty capsules received.
Reason Does Not Meet Monograph: NEW GPC INC. has recalled multiple Over-the-Counter Drug Products due to lack of drug listing, lack of OTC drug labeling…
Reason Labeling: Label Error On Declared Strength: Trelstar 11.25 mg labeled carton/kit contained a vial labeled as 3.75 mg instead of a vial being labeled…
Reason Marketed Without An Approved NDA/ANDA: FDA analyses detected the presence of phenolphthalein, N-di-Desmethylsibutramine, and trace amounts of…
Reason Contraceptive Tablets out of Sequence: A placebo tablet was found in a row of active tablets.
Reason Marketed Without an Approved NDA/ANDA; products have been found to contain tadalafil, the active ingredient in an FDA approved product used to treat…
Reason Marketed Without an Approved NDA/ANDA; products have been found to contain tadalafil, the active ingredient in an FDA approved product used to treat…
Reason Microbial Contamination of Non-Sterile Products: Arthritis Relief Cream failed microbiological specifications.
Reason Defective Container: Pump head detaching from the canister unit upon removal of the overcap.
Reason Lack of Assurance of Sterility: There is the potential for the solution to leak from the seal of the fill tube to the bag.
Reason Adulterated Presence of Foreign Tablets: This product is being recalled becaiuse 30 valacyclovir hydrochloride tablets USP 500 mg were discovered in…
Reason Labeling: Label Mix up; product labeled to contain Nebivolol tablets actually contained Pramipexole Dihydrochloride tablets
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