367 FDA recalls mention Amino. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Amino.
Reason Labeling: Not Elsewhere Classified: Pentrexcilina Tablets and Pentrexcilina Liquid are being recalled because the product labels are misleading…
Reason Labeling: Not Elsewhere Classified: This unit dose product is being recalled because the product's name includes the word "Children's" which is…
Reason Subpotent; 12 month time point for the active ingredient Phenylephrine HCl.
Reason Superpotent (Multiple Ingredient) Drug: Oversized tablets resulting in superpotent assays of both the hydrocodone and acetaminophen components.
Reason Superpotent (Multiple Ingredient) Drug: Complaint received of oversized tablets.
Reason Superpotent (Multiple Ingredient) Drug: There is the potential for oversized and superpotent tablets.
Reason Superpotent (Multiple Ingredient) Drug: Confirmed customer complaints of oversized tablets resulting in superpotent assays of both the hydrocodone…
Reason Presence of Particulate Matter: The firm initiated the recall due to visible presence of particulate matter.
Reason Incorrect/Undeclared Excipients: The firm recalled specific lots of Walgreens brand Aspirin Free Tension Headache Caplets due to the presence of…
Reason Labeling; labeled with incorrect EXP Date; Incorrect expiration date printed on the outer packaging. Package incorrectly states 5/2014 should…
Reason Impurities/Degradation Products: exceeded specification at 3 month stability testing
Reason Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all Sterile Human Drugs distributed between 11/21/2011 and 05/21/2012 because…
Reason CGMP Deviations: This product is being recalled because expired flavoring was used in the manufacturing of these lots.
Reason Subpotent (Multiple Ingredient) Drug: Low out of specification assay results for the hydrocodone bitartrate ingredient was found.
Reason Adulterated Presence of Foreign Tablets: Customer complaint that some Endocet 10 mg/325 mg tablets were found mixed in a bottle with Endocet 10…
Reason Labeling: Label Mix-up: This recall was initiated after identifying that the label statement on the blister strip regarding the maximum number of…
Reason Labeling: Label Mix-up: This recall was initiated after identifying that the label statement on the blister strip regarding the maximum number of…
Tell us which medications you take. If the FDA recalls one, we email you - in plain English, with what to do. Free.