AirWick Fresh New Day® aerosol air fresheners - "Fresh Linen" and "Fresh Waters" scents
Summary
CPSC recalled AirWick Fresh New Day® aerosol air fresheners - "Fresh Linen" and "Fresh Waters" scents by RB Manufacturing LLC "Reckitt", of Parsippany, New Jersey. Hazard: A single batch of the aerosol air fresheners is missing a corrosion inhibitor, which can lead to corrosion and rupture of the metal can and expulsion of the contents, posing injury and laceration hazards. In addition, corrosion of the container can result in leakage, posing a risk of skin and eye irritation upon contact.. Remedy: Consumers should immediately stop using the recalled air fresheners, wrap the product in several layers of paper, and dispose in accordance with state and local requirements. Use caution to avoid skin and eye contact if the can appears to be leaking. Reckitt is offering consumers a voucher for a free replacement Fresh New Day aerosol air freshener. Consumers should contact Reckitt to submit a photo of the recalled can, along with their contact information and written confirmation that they will dispose of the can to receive a voucher for a free replacement..
Details
Source
cpsc
External ID
23035
Action Date
2022-11-03
Status
Ongoing
Category
product
Product Description
This recall involves AirWick Fresh New Day aerosol air fresheners in 8-ounce aerosol cans in "Fresh Linen" scent (blue and white can, white cap, green Airwick logo, UPC 0-62338-74734-7) and "Fresh Waters" scent (green and white can, white cap, green Airwick logo, UPC 0-62338-77002-4) with batch code B22077-NJ and date code 18/03/22. The batch and date codes are printed on the bottom of the can, and the UPC is printed on the rear label, adjacent to the barcode.
Context & Analysis
RB Manufacturing LLC "Reckitt", of Parsippany, New Jersey has 2 FDA actions in our database, including 1 recall.
Frequently Asked Questions
How often does RB Manufacturing LLC "Reckitt", of Parsippany, New Jersey have FDA actions?
RB Manufacturing LLC "Reckitt", of Parsippany, New Jersey has 2 FDA actions in our database, including 1 recall and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Use the link above to view the complete official filing. You can also use the openFDA API to query this record programmatically.
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