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Vintage Pharmaceuticals LLC, Recalls
12 recalls on record · July 18, 2012 to May 31, 2017 · Drugs
Recalls by year
12
13
15
17
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
May 31, 2017DrugsFDA
Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals recalls HYDROCORTISONE LOTION, USP, 2.5%, 2 FL OZ (59 mL) bottle, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVI
Hazard: Superpotent Drug: above specification for the assay.
February 1, 2017DrugsFDA
Vintage Pharmaceuticals LLC dba Qualitest Pharmaceuticals recalls DEXAMETHASONE ELIXIR, USP, 0.5 mg/5 mL, 8 fl.oz., Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL,
Hazard: Failed Impurities/ Degradation Specifications
January 11, 2017DrugsFDA
Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals recalls TEMAZEPAM CAPSULES USP, 7.5 mg, 100 count bottles, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL
Hazard: Failed Stability Specifications
November 25, 2015DrugsFDA
Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals recalls HYDROCHLOROTHIAZIDE CAPSULES, USP, 12.5 mg, 3000 count bottles, Rx only, Manufactured for: Qualitest Pharmaceuticals, In
Hazard: Presence of Particulate Matter.
November 11, 2015DrugsFDA
Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals recalls RANITIDINE SYRUP (RANITIDINE ORAL SOLUTION, USP) 15 mg/mL (75 mg/5 mL), 473 mL (16 fl oz), Rx only. Manufactured for: Q
Hazard: Failed Stability Specifications: Out of Specification results obtained for preservative butylparaben.
September 9, 2015DrugsFDA
Vintage Pharmaceuticals LLC dba Qualitest Pharmaceuticals recalls Lisinopril Tablets, USP, 40 mg, a) 45-count bottle (NDC 0603-4214-60), b) 500-count bottle (NDC 0603-4214-28), Rx Only,
Hazard: Failed Dissolution Specifications
August 26, 2015DrugsFDA
Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals recalls AMPICILLIN CAPSULES, USP, 250 mg, 500 count bottles, Rx only, Manufactured for: DAVA Pharmaceuticals, Inc., Fort Lee, NJ
Hazard: Labeling: Incorrect Or Missing Package Insert: Product is labeled with unapproved labeling.
February 6, 2013DrugsFDA
Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals recalls Hydrocodone bitartrate and acetaminophen Tablets, USP, 10 mg/500 mg, packaged in a) 30-count bottles, NDC 0603-3888-16;
Hazard: Superpotent (Multiple Ingredient) Drug: Complaint received of oversized tablets.
November 28, 2012DrugsFDA
Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals recalls HYDROCODONE BITARTRATE and ACETAMINOPHEN TABLETS, USP, 10 mg/500 mg, 100-count bottle, Rx only, Mfg. for: QUALITEST PHA
Hazard: Superpotent (Multiple Ingredient) Drug: Confirmed customer complaints of oversized tablets resulting in superpotent assays of both the hydrocodone and acetaminophen components.
October 31, 2012DrugsFDA
Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals recalls Perphenazine Tablets, USP, 8 mg, 100-count tablets per bottle, Manufactured for: Qualitest Pharmaceuticals, Huntsville,
Hazard: Tablet Separation: Possibility of cracked or split coating on the tablets.
July 25, 2012DrugsFDA
Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals recalls HYDROXYZINE HYDROCHLORIDE ORAL SOLUTION, USP, 10 mg/5 mL, 1 PINT (473 mL) bottle, Rx only, Mfg. for: QUALITEST PHARMACE
Hazard: Impurities/Degradation Products: High Out of Specification results for a known impurity resulted at the 12-month room temperature time point.
July 18, 2012DrugsFDA
Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals recalls HYDROCORTISONE and ACETIC ACID OTIC SOLUTION, USP, 10 mL bottle, Rx only, Mfg. for: QUALITEST PHARMACEUTICALS, HUNTSVIL
Hazard: Impurities/Degradation Products: Out of specificiation results for impurities at the 18-month room temperature time point.