Why it was recalled
Incorrect Product Formulation: product contains dexamethasone instead of hydrocortisone.
Product description
PIYANPING Anti-Itch (hydrocortisone) Lotion, 1%, Net Wt. 0.67 oz (20g) tube, Manufactured By: Jimin Pharmaceutial Co., LTD., Distributor: Lucky Mart, El Monte, CA 91733, NDC 68085-8012-4.
Lot numbers, UPCs & expiration codes
Lot #: C16001, C16002, Exp 12/18
Where it was sold
Nationwide in the USA
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-0031-2018
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- Aug 29, 2017
- FDA report date
- Nov 1, 2017
- Quantity
- 13,800 tubes
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Lucky Mart Inc.
Original FDA data
Every field from FDA enforcement report D-0031-2018, exactly as published.
Show all FDA fields
- City
- South El Monte
- State
- CA
- Status
- Terminated
- Country
- United States
- Event ID
- 78051
- Address
- 2210 N Seaman Ave
- Code information
- Lot #: C16001, C16002, Exp 12/18
- Postal code
- 91733-1926
- Report date
- Nov 1, 2017
- Product type
- Drugs
- Recall number
- D-0031-2018
- Classification
- Class I
- Recalling firm
- Lucky Mart Inc.
- Product quantity
- 13,800 tubes
- Termination date
- Oct 30, 2018
- Reason for recall
- Incorrect Product Formulation: product contains dexamethasone instead of hydrocortisone.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- PIYANPING Anti-Itch (hydrocortisone) Lotion, 1%, Net Wt. 0.67 oz (20g) tube, Manufactured By: Jimin Pharmaceutial Co., LTD., Distributor: Lucky Mart, El Monte, CA 91733, NDC 68085-8012-4.
- Distribution pattern
- Nationwide in the USA
- Recall initiation date
- Aug 29, 2017
- Initial firm notification
- Letter
- Center classification date
- Oct 24, 2017