The Recall Desk

Manufacturer

Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals

12 recalls in our database name Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals as the manufacturing or recalling firm.

What the numbers show

Total
12
Critical
1
Severe
1
Most recent
2017-05-31

Of the 12 recalls from Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals we have scored against our rubric, 1 (8%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1 (8%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–12 of 12

  • LowFDA (Drugs)·D-0859-2017·2017-05-31

    Qualitest Recalls Hydrocortisone Lotion for Excessive Potency

    Qualitest Pharmaceuticals is recalling 109,620 bottles of Hydrocortisone Lotion, USP, 2.5% because the product is superpotent, meaning it contains more active ingredient than specified.

    Product
    HYDROCORTISONE LOTION, USP, 2.5%, 2 FL OZ (59 mL) bottle, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC 0603-7785-52.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0438-2017·2017-02-01

    Qualitest Recalls Dexamethasone Elixir Due to Failed Impurity Specifications

    Vintage Pharmaceuticals is recalling 2,568 bottles of Dexamethasone Elixir because the product failed impurity and degradation specifications.

    Product
    DEXAMETHASONE ELIXIR, USP, 0.5 mg/5 mL, 8 fl.oz., Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL, NDC 0603-1147-56
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0326-2017·2017-01-11

    Qualitest Recalls Temazepam Capsules Due to Failed Stability Specifications

    Vintage Pharmaceuticals is recalling 1,200 bottles of Temazepam 7.5 mg capsules because they failed stability specifications. The affected lot is distributed nationwide.

    Product
    TEMAZEPAM CAPSULES USP, 7.5 mg, 100 count bottles, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC 0603-5891-21
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0232-2016·2015-11-25

    Qualitest Recalls Hydrochlorothiazide Capsules Due to Particulate Matter

    Vintage Pharmaceuticals is recalling 912 bottles of 12.5 mg Hydrochlorothiazide capsules because of the presence of particulate matter.

    Product
    HYDROCHLOROTHIAZIDE CAPSULES, USP, 12.5 mg, 3000 count bottles, Rx only, Manufactured for: Qualitest Pharmaceuticals, Inc., Huntsville, AL 35811, NDC: 0603-3855-93.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0162-2016·2015-11-11

    Qualitest Recalls Ranitidine Syrup Due to Preservative Stability Failure

    Vintage Pharmaceuticals is recalling specific lots of Ranitidine Syrup because preservative levels failed stability specifications.

    Product
    RANITIDINE SYRUP (RANITIDINE ORAL SOLUTION, USP) 15 mg/mL (75 mg/5 mL), 473 mL (16 fl oz), Rx only. Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC: 0603-9418-58.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1406-2015·2015-09-09

    Qualitest Recalls Lisinopril Tablets for Failed Dissolution Specifications

    Vintage Pharmaceuticals is recalling 8,705 bottles of Lisinopril 40 mg tablets because they failed dissolution specifications. The affected lots were distributed nationwide and in Puerto Rico.

    Product
    Lisinopril Tablets, USP, 40 mg, a) 45-count bottle (NDC 0603-4214-60), b) 500-count bottle (NDC 0603-4214-28), Rx Only, Manufactured for: Qualitest Pharmaceuticals, Huntsville, AL 35811
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1350-2015·2015-08-26

    Qualitest Recalls Ampicillin Capsules Due to Unapproved Labeling

    Vintage Pharmaceuticals LLC is recalling 360 bottles of Ampicillin Capsules, USP, 250 mg, because they are labeled with unapproved labeling.

    Product
    AMPICILLIN CAPSULES, USP, 250 mg, 500 count bottles, Rx only, Manufactured for: DAVA Pharmaceuticals, Inc., Fort Lee, NJ, By: Suir Pharma Ireland Ltd., Clonmel, Ireland, NDC: 67253-180-50
    Category
    Drug
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-138-2013·2013-02-06

    Qualitest Recalls Hydrocodone and Acetaminophen Tablets Due to Oversized Size

    Qualitest Pharmaceuticals is recalling 897,379 bottles of Hydrocodone bitartrate and acetaminophen tablets because a complaint reported the tablets were oversized.

    Product
    Hydrocodone bitartrate and acetaminophen Tablets, USP, 10 mg/500 mg, packaged in a) 30-count bottles, NDC 0603-3888-16; b) 60-count bottles, NDC 0603-3888-20; c) 90-count bottles, NDC 0603-3888-02; d) 100-count bottles, NDC 0603-3888-21; e) 120-count bottles, NDC 0603-3888-22; f)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-057-2013·2012-11-28

    Qualitest Recalls Hydrocodone and Acetaminophen Tablets Due to Oversized Pills

    Vintage Pharmaceuticals is recalling 14,445 bottles of hydrocodone and acetaminophen tablets because confirmed complaints found oversized pills with superpotent drug levels.

    Product
    HYDROCODONE BITARTRATE and ACETAMINOPHEN TABLETS, USP, 10 mg/500 mg, 100-count bottle, Rx only, Mfg. for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC 0603-3888-21
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-010-2013·2012-10-31

    Qualitest Recalls Perphenazine Tablets Due to Cracked Coating

    Vintage Pharmaceuticals is recalling 2,755 bottles of Perphenazine 8 mg tablets due to a possibility of cracked or split tablet coatings.

    Product
    Perphenazine Tablets, USP, 8 mg, 100-count tablets per bottle, Manufactured for: Qualitest Pharmaceuticals, Huntsville, AL 35811, NDC 0603-5092-21.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1417-2012·2012-07-25

    Qualitest Recalls Hydroxyzine Hydrochloride Oral Solution Due to Impurity

    Vintage Pharmaceuticals is recalling 73,746 bottles of Hydroxyzine Hydrochloride Oral Solution because high levels of a known impurity were detected.

    Product
    HYDROXYZINE HYDROCHLORIDE ORAL SOLUTION, USP, 10 mg/5 mL, 1 PINT (473 mL) bottle, Rx only, Mfg. for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC 0603-1310-58, UPC 3 0603-1310-58 4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1411-2012·2012-07-18

    Qualitest Recalls Hydrocortisone and Acetic Acid Otic Solution Due to Impurities

    Vintage Pharmaceuticals is recalling 54,431 bottles of Hydrocortisone and Acetic Acid Otic Solution because impurity levels exceeded specifications.

    Product
    HYDROCORTISONE and ACETIC ACID OTIC SOLUTION, USP, 10 mL bottle, Rx only, Mfg. for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811; NDC 0603-7039-39; UPC 3 0603-7039-39 7.
    Category
    Drug
    Distribution
    Distributed nationwide