Why it was recalled
Defective Container: products showed leakage (bubbles, foaming) of propellant and product from the container valve cup area.
Product description
Neutrogena Elevated 4-Holiday Trays (contains Neutrogena Deep Clean Purifying Whipped Foam Cleanser) Case Code: 00070501302866
Lot numbers, UPCs & expiration codes
Lot #: 2617RT1, 2617RT2, 2627RT2, 2637RT1, 2647RT1, 2657RT1, 2627RT2, EXP 05/2019
Where it was sold
Product was distributed nationwide
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-0245-2018
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Dec 7, 2017
- FDA report date
- Feb 7, 2018
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Johnson & Johnson
Original FDA data
Every field from FDA enforcement report D-0245-2018, exactly as published.
Show all FDA fields
- City
- Skillman
- State
- NJ
- Status
- Terminated
- Country
- United States
- Event ID
- 78610
- Address
- 199 Grandview Rd
- Code information
- Lot #: 2617RT1, 2617RT2, 2627RT2, 2637RT1, 2647RT1, 2657RT1, 2627RT2, EXP 05/2019
- Postal code
- 08558-1311
- Report date
- Feb 7, 2018
- Product type
- Drugs
- Recall number
- D-0245-2018
- Classification
- Class II
- Recalling firm
- Johnson & Johnson
- Termination date
- Sep 9, 2019
- Reason for recall
- Defective Container: products showed leakage (bubbles, foaming) of propellant and product from the container valve cup area.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Neutrogena Elevated 4-Holiday Trays (contains Neutrogena Deep Clean Purifying Whipped Foam Cleanser) Case Code: 00070501302866
- Distribution pattern
- Product was distributed nationwide
- Recall initiation date
- Dec 7, 2017
- Initial firm notification
- Letter
- Center classification date
- Jan 29, 2018