Home / Recalls / Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals / D-0859-2017

D-0859-2017 Class III Terminated

Recalled by Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals — Huntsville, AL

Recall Details

Product Type
Drugs
Report Date
May 31, 2017
Initiation Date
May 8, 2017
Termination Date
May 2, 2018
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
109,620 bottles

Product Description

HYDROCORTISONE LOTION, USP, 2.5%, 2 FL OZ (59 mL) bottle, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC 0603-7785-52.

Reason for Recall

Superpotent Drug: above specification for the assay.

Distribution Pattern

Nationwide in the USA and Puerto Rico.

Code Information

Lot #: 0000004961, Exp. 05/17; 0000005197, 0000005198, 0000005199, Exp. 07/17; 0000005201, 0000005202, 0000005203, 0000005204, Exp. 09/17; 0000005200, 0000007998, 0000007999, 0000007022, Exp. 12/17; 0000009176, Exp. 04/18; 0000012281, 0000012282, Exp. 12/18

Other recalls by Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals

  • D-0326-2017 Class III — TEMAZEPAM CAPSULES USP, 7.5 mg, 100 count bottles, Rx only, Manufactured for: QU (December 22, 2016)
  • D-0162-2016 Class III — RANITIDINE SYRUP (RANITIDINE ORAL SOLUTION, USP) 15 mg/mL (75 mg/5 mL), 473 mL ( (October 21, 2015)
  • D-0232-2016 Class II — HYDROCHLOROTHIAZIDE CAPSULES, USP, 12.5 mg, 3000 count bottles, Rx only, Manufac (October 7, 2015)
  • D-1350-2015 Class III — AMPICILLIN CAPSULES, USP, 250 mg, 500 count bottles, Rx only, Manufactured for: (August 13, 2015)