Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals recalls
Every recall we track for Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals — 12 in all, from 2012–2017 — plus the complaints and injury reports the public filed about them. 2 are rated “stop using now”.
Recalls per year, by danger level
2 recalls since 2017.
All FDA recall records for Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 1 | 1 | 2 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals recalls before 2017
Recalls on record by year.
What to do if you have a recalled Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals product
- Match the NDC and lot number on your bottle or box to the recall.
- Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first.
- Report side effects to FDA MedWatch.
All Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals recalls
12 shown- Lower riskDrug
Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals recalls HYDROCORTISONE LOTION, USP, 2.5%, 2 FL OZ (59 mL) bottle, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS,
Qualitest Pharmaceuticals recalls hydrocortisone lotion with high potency levels. This may cause excessive skin reactions. Check lot numbers and contact for details.
Qualitest PharmaceuticalsMay 8, 2017 - UnratedDrug
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,
Qualitest Pharmaceuticals recalls Dexamethasone Elixir (0.5 mg/5mL, :8 fl.oz.) due to failed impurities and degradation specifications. Rx only product with NDC 0603-1147-56, lot 0000007104, exp 05/17.
Qualitest PharmaceuticalsJan 16, 2017 - Lower riskDrug
Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals recalls TEMAZEPAM CAPSULES USP, 7.5 mg, 100 count bottles, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL
Qualitest Pharmaceuticals recalls 7.5mg TEMAZEPAM capsules due to failed stability tests. These prescription-only capsules may degrade over time, posing safety risks. Check your prescription label for NDC 0603-5891-21.
Qualitest PharmaceuticalsDec 22, 2016 - Use cautionDrug
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:
Qualitest recalls specific lots of Ranitidine Syrup because preservative levels failed stability specifications. Check your bottle's lot number and expiry date.
Qualitest PharmaceuticalsOct 21, 2015 - Use cautionDrug
Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals recalls HYDROCHLOROTHIAZIDE CAPSULES, USP, 12.5 mg, 3000 count bottles, Rx only, Manufactured for: Qualitest Pharmaceuticals,
Qualitest recalls 12.5 mg Hydrochlorothiazide capsules due to particulate matter presence. Check lot numbers T084M14A, T085M14A, T086M14A.
Qualitest PharmaceuticalsOct 7, 2015 - Use cautionDrug
Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals recalls AMPICILLIN CAPSULES, USP, 250 mg, 500 count bottles, Rx only, Manufactured for: DAVA Pharmaceuticals, Inc., Fort Lee,
Qualitest recalls 360 bottles of Ampicillin Capsules due to unapproved labeling. Check your lot number for details.
Qualitest PharmaceuticalsAug 13, 2015 - Use cautionDrug
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,
Qualitest recalls specific lots of Lisinopril Tablets, USP 40 mg due to failed dissolution specifications. Check your bottle's NDC and lot number.
Qualitest PharmaceuticalsJul 29, 2015 - Stop using nowDrug
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;
Qualitest Pharmaceuticals is recalling specific lots of Hydrocodone bitartrate and acetaminophen tablets because complaints of oversized tablets were received.
Qualitest PharmaceuticalsDec 6, 2012 - Use cautionDrug
Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals recalls Perphenazine Tablets, USP, 8 mg, 100-count tablets per bottle, Manufactured for: Qualitest Pharmaceuticals, Huntsville,
Qualitest Pharmaceuticals recalls 2,755 bottles of Perphenazine Tablets 8 mg due to tablet separation. Check your lot number and expiration date.
Qualitest PharmaceuticalsOct 11, 2012 - Stop using nowDrug
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
Qualitest recalls 10mg/500mg hydrocodone and acetaminophen tablets due to oversized pills causing superpotent drug levels. Check your lot number C1440512A.
Qualitest PharmaceuticalsSep 10, 2012 - UnratedDrug
Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals recalls HYDROCORTISONE and ACETIC ACID OTIC SOLUTION, USP, 10 mL bottle, Rx only, Mfg. for: QUALITEST PHARMACEUTICALS,
Qualitest recalls specific lots of Hydrocortisone and Acetic Acid Otic Solution, USP (10 mL) due to impurity specification failures. Check your lot numbers.
Qualitest PharmaceuticalsJul 6, 2012 - UnratedDrug
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
Qualitest recalls specific lots of Hydroxyzine Oral Solution due to high levels of a known impurity. Check your bottle's lot number and expiration date immediately.
Qualitest PharmaceuticalsJul 6, 2012
Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals recall questions
How many recalls has Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals had?
12 recalls from Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals are on record with U.S. safety agencies, from 2012–2017.
What is the most recent Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals recall?
Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals recalls HYDROCORTISONE LOTION, USP, 2.5%, 2 FL OZ (59 mL) bottle, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS,, dated May 8, 2017. Every Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals recall is listed on this page, newest first.
What should I do if I have a recalled Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals product?
Match the NDC and lot number on your bottle or box to the recall. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first. Report side effects to FDA MedWatch.
How do I get alerts for new Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.