0.25% Acetic Acid Irrigation USP
Presence of Particulate Matter: identified as polyethylene, which is consistent with the material used to manufacture the contain cap
14,806 recalls, newest first
Presence of Particulate Matter: identified as polyethylene, which is consistent with the material used to manufacture the contain cap
Failed Stability Specifications
GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.
GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.
GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.
GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.
GMP Deviations: manufacturing of API material did not meet GMP and quality requirements.
Failed Impurities/Degradation Specifications: High out of specification test result for the Moexipril Diketopiperazine impurity was obtained during routine stability testing.
Failed Stability Specifications: Product stability testing results did not meet specifications for iron content.
Microbial Contamination of Non-Sterile Products: potentially contamination with the bacteria Burkholderia cepacia
Presence of Foreign Substance: Reports have been received of damaged StripPax packets containing silica gel desiccant potentially allowing the silica gel granules to make contact with Auryxia tablets in the bottle.
Marketed without an approved NDA/ANDA: FDA analysis found the product to contain undeclared sibutramine.
Defective Container: products showed leakage (bubbles, foaming) of propellant and product from the container valve cup area.
Defective Container: products showed leakage (bubbles, foaming) of propellant and product from the container valve cup area.
Defective Container: products showed leakage (bubbles, foaming) of propellant and product from the container valve cup area.
Labeling: Incorrect or Missing Lot and/or Exp Date - product label was missing lot number and beyond use date.
Labeling: Label Error on Declared Strength. A single syringe labeled as 150 mg/1.0 mL was found packaged in a blister labeled as 120 mg/mL
Presence of Particulate Matter: One vial from a lot of Pantoprazole Sodium for Injection (40 mg) contained a piece of glass
Labeling: Label Mix-Up.some bottles labeled as Gabapentin 800 mg contain Gabapentin 600 mg
Subpotent Drug: One lot of Viokace is being recalled since product stability testing results did not meet the specifications for enzyme profile.
Marketed without an Approved NDA/ANDA; product found to be tainted with sildenafil
Lack of sterility assurance.
Lack of sterility assurance.
Lack of sterility assurance.
Lack of sterility assurance.