Aveeno Daily Moisturizing lotion Fragrance Free with Soothing Oat & Rich Emollients, Net Wt. 5 oz (141 g), Distributed b
Summary
The FDA issued a Class II for Aveeno Daily Moisturizing lotion Fragrance Free with Soothing Oat & Rich Emollie by Family Dollar Stores, Llc.. Reason: cGMP deviations: product stored outside of labeled temperature requirements..
Details
Source
Drug Recall
External ID
D-0981-2022
Action Date
2022-06-08
Status
Ongoing
Category
drug
Product Description
Aveeno Daily Moisturizing lotion Fragrance Free with Soothing Oat & Rich Emollients, Net Wt. 5 oz (141 g), Distributed by Johnson & Johnson Consumer, Inc. Skillman, NJ 08558, UPC 3 81137-001530 7
Lot/Code Info: SKUs 2005444
Quantity Affected: Unknown
Reason for Recall
cGMP deviations: product stored outside of labeled temperature requirements.
Distribution
USA Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2022-05-17
Company
Chesapeake, VA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 105 drug recalls issued in the same week, part of 272 drug-related FDA actions this month.
Family Dollar Stores, Llc. has 149 FDA actions in our database, including 149 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Family Dollar Stores, Llc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Family Dollar Stores, Llc. have FDA actions?
Family Dollar Stores, Llc. has 149 FDA actions in our database, including 149 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0981-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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