CLASS II Drug recall · Reported 31 Oct 2012 · FDA Enforcement Report
Perphenazine Tablets recalled by Vintage Pharmaceuticals
Vintage Pharmaceuticals is recalling Perphenazine Tablets, USP per, distributed nationwide in the US. The recall was initiated on 11 Oct 2012 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-010-2013
- FDA event ID
- 63502
- Recalling firm
- Vintage Pharmaceuticals, Huntsville, AL
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 11 Oct 2012
- FDA classified
- 22 Oct 2012
- Reported
- 31 Oct 2012
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
Timeline
| 11 Oct 2012 | Recall initiated by company | |
| 22 Oct 2012 | Classified by FDA | +11 days |
| 31 Oct 2012 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Tablet Separation: Possibility of cracked or split coating on the tablets.
Product as listed by the FDA
Perphenazine Tablets, USP, 8 mg, 100-count tablets per bottle, Manufactured for: Qualitest Pharmaceuticals, Huntsville, AL 35811, NDC 0603-5092-21.
Where it was distributed
Nationwide and Puerto Rico
Questions about this recall
Why was it recalled?
Tablet Separation: Possibility of cracked or split coating on the tablets.
Which lots are affected?
Lot C1130511A, Exp 5/13
Where was it sold?
Nationwide and Puerto Rico
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Vintage Pharmaceuticals
All 7| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Dexamethasone Elixir, USP, 0.5 mg recalled by Vintage Pharmaceuticals | Vintage Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Lisinopril Tablets, USP, 40 mg, a) bottle recalled | Vintage Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS I | Hydrocodone bitartrate and acetaminophen Tablets, USP, 10 mg/500 mg recalled | Vintage Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS I | Hydrocodone Bitartrate and Acetaminophen Tablets, USP, 10 mg/500 mg recalled | Vintage Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS III | Hydroxyzine Hydrochloride Oral Solution, USP, 10 mg/, 1 Pint recalled | Vintage Pharmaceuticals | Potency & Assay | Nationwide |
Other Perphenazine recalls
All 4| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Perphenazine, Tablet, 16 mg recalled by Aidapak Services | Aidapak Services | Labeling Errors | 4 states |
| Drug | CLASS II | Perphenazine, Tablet, 16 mg recalled by Aidapak Services | Aidapak Services | Labeling Errors | 4 states |
| Drug | CLASS II | Perphenazine, Tablet, 8 mg recalled by Aidapak Services | Aidapak Services | Labeling Errors | 4 states |