Why it was recalled
cGMP deviations
Product description
DILOTAB II, SINUS AND COLD RELIEF NON DROWSY (acetaminophen 325 mg, Phenylephrine HCl 5 mg) 2 tablet packets, Dist. by ZEE Medical Distributors, LLC Mason, OH 45040, NDC 42961-052-03
Lot numbers, UPCs & expiration codes
Lot #: AK9548, (L) 106, Exp. Date 04/2022; AK9647, (L)103, Exp. Date 06/2022; AK9598, Exp. Date 05/2022
Where it was sold
Nationwide within the United States
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0490-2022
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Jan 24, 2022
- FDA report date
- Feb 9, 2022
- Quantity
- 2,685,700 packets
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Ultra Seal Corporation
Original FDA data
Every field from FDA enforcement report D-0490-2022, exactly as published.
Show all FDA fields
- City
- New Paltz
- State
- NY
- Status
- Terminated
- Country
- United States
- Event ID
- 89464
- Address
- 521 Main St
- Code information
- Lot #: AK9548, (L) 106, Exp. Date 04/2022; AK9647, (L)103, Exp. Date 06/2022; AK9598, Exp. Date 05/2022
- Postal code
- 12561-1609
- Report date
- Feb 9, 2022
- Product type
- Drugs
- Recall number
- D-0490-2022
- Classification
- Class II
- Recalling firm
- Ultra Seal Corporation
- Product quantity
- 2,685,700 packets
- Termination date
- Oct 16, 2023
- Reason for recall
- cGMP deviations
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- DILOTAB II, SINUS AND COLD RELIEF NON DROWSY (acetaminophen 325 mg, Phenylephrine HCl 5 mg) 2 tablet packets, Dist. by ZEE Medical Distributors, LLC Mason, OH 45040, NDC 42961-052-03
- Distribution pattern
- Nationwide within the United States
- Recall initiation date
- Jan 24, 2022
- Initial firm notification
- Letter
- Center classification date
- Jan 31, 2022