Yes — there is an active recall. 34 ongoing FDA recalls mention Amino (367 total). Check the affected lots below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Amino. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed.
Reason Superpotent Drug: Bio-Pharm, Inc. is initiating a recall of one lot of Acetaminophen Oral Suspension Liquid 160mg/5mL failure of the product assay at…
Reason Marketed without an Approved NDA/ANDA; IM and SQ injectable products are being recalled because the manufacturing firm is not registered with the FDA…
Reason Subpotent Drug: Phenylephrine component is subpotent.
Reason Failed Tablet/Capsule Specifications; Product contains broken tablets.
Reason Lack of Assurance of Sterility; potential leakage from administrative port.
Reason Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve…
Reason Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve…
Reason Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve…
Reason Presence of Particulate Matter: B. Braun Medical Inc. is recalling several injectable products due to visible particulate matter found in reserve…
Reason Presence of Particulate Matter: Particulate matter includes wood, sodium citrate and dextrose.
Reason Presence of Particulate Matter: Particulate matter includes wood, sodium citrate and dextrose.
Reason Presence of Particulate Matter: Particulate matter includes wood, sodium citrate and dextrose.
Reason Lack of Assurance of Sterility; Drug product leaking from container therefore sterility cannot be assured
Reason Defective Delivery System: There is a remote potential that cartons of product could be co-packaged with an oral dosing syringe without dose markings.
Reason Defective Delivery System: There is a remote potential that cartons of product could be co-packaged with an oral dosing syringe without dose markings.
Reason Defective Delivery System: There is a remote potential that cartons of product could be co-packaged with an oral dosing syringe without dose markings.
Reason Defective Delivery System: There is a remote potential that cartons of product could be co-packaged with an oral dosing syringe without dose markings.
Reason Presence of Foreign Tablets/Capsules: 20 tablets of Oxycodone/APAP 7.5/500 mg were found in a sealed 100 count bottle of Oxycodone and Acetaminophen…
Reason Presence of Particulate Matter: Confirmed customer complaint of particulate matter, identified as a human hair, visible in the injection port and…
Reason Defective Container: Defective bottles may not have tamper evident seals properly seated, and therefore it may be difficult to determine if the…
Reason Incorrect/ Undeclared Excipients: NyQuil Liquid Original bottles were inadvertently overwrapped with NyQuil Liquid Cherry information as a result the…
Reason CGMP Deviations: The recalled acetaminophen tablet lot was not manufactured under current good manufacturing practices as noted by a recent…
Reason Lack of Assurance of Sterility; FDA inspectional findings resulted in concerns associated with quality control procedures that impacted sterility…
Reason Subpotent drug: Two lots of Oxycodone and Acetaminophen Capsules, USP 5/500 mg are being recalled due to low out of specification (OOS) assay result…
Reason Unit Dose Mispackaging: Product packaging defect which could result in code date smearing, incomplete blister card cuts, and missing or incorrectly…
Tell us which medications you take. If the FDA recalls one, we email you - in plain English, with what to do. Free.