CLASS II Drug recall · Reported 12 Jun 2013 · FDA Enforcement Report
Dallergy Chewable Tablets, Antihistamine, Nasal Decongestant recalled
TG United is recalling Dallergy Chewable Tablets, Antihistamine, Nasal Decongestant, 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-518-2013
- 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
Dallergy CHEWABLE TABLETS, Antihistamine, Nasal Decongestant, 100 count bottle, OTC, Manufactured for: Laser Pharmaceuticals, LLC, Greenville, SC 29615, NDC 16477-152-01
Where it was distributed
FL, MS, SC, LA and TX
Questions about this recall
Is Dallergy Chewable Tablets, Antihistamine, Nasal Decongestant recalled?
Yes. TG United recalled Dallergy Chewable Tablets, Antihistamine, Nasal Decongestant on 30 Jan 2013. The recall is Class II and its status is Terminated. Recall number D-518-2013.
Why was it recalled?
CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Which lots are affected?
Lot# 12B001 Exp. 01/14; Lot# 12B001 Exp. 01/14; Lot# 12B002 Exp 01/14; Lot# 12F013 Exp. 05/2014; Lot# 12F013 Exp. 05/2014.
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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