CLASS II Drug recall · Reported 12 Jun 2013 · FDA Enforcement Report
Poly-Vent DM Tablets, Cough Suppressant, Expectorant, Nasal recalled
TG United is recalling Poly-Vent DM Tablets, Cough Suppressant, Expectorant, Nasal, distributed in Florida, Louisiana, Mississippi, South Carolina, Texas. The recall was initiated on 30 Jan 2013 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-530-2013
- FDA event ID
- 64188
- Recalling firm
- TG United, Brooksville, FL
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 30 Jan 2013
- FDA classified
- 4 Jun 2013
- Reported
- 12 Jun 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Manufacturing (CGMP) Deviations
- Drug class
- Nasal Sprays
Timeline
| 30 Jan 2013 | Recall initiated by company | |
| 4 Jun 2013 | Classified by FDA | +125 days |
| 12 Jun 2013 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Product as listed by the FDA
Poly-Vent DM Tablets, Cough Suppressant, Expectorant, Nasal Decongestant, 60 count bottle, OTC, Distributed by: Poly Pharmaceuticals, Quitman, MS 39355 NDC 50991-309-60
Where it was distributed
FL, MS, SC, LA and TX
Questions about this recall
Is Poly-Vent DM Tablets, Cough Suppressant, Expectorant, Nasal recalled?
Yes. TG United recalled Poly-Vent DM Tablets, Cough Suppressant, Expectorant, Nasal on 30 Jan 2013. The recall is Class II and its status is Terminated. Recall number D-530-2013.
Why was it recalled?
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Which lots are affected?
Lot# 11F005 Exp 05/13; Lot# 11M008 Exp 11/13; Lot# 12J003 Exp 08/12.
Where was it sold?
FL, MS, SC, LA and TX
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 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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