BADGER 50, ADVENTURE SPORT MINERAL SUNSCREEN WITH CLEAR ZINC, (uncoated 25% zinc oxide), 2.4 oz., Tin, W.S. Badger Compa
Summary
The FDA issued a Class III for BADGER 50, ADVENTURE SPORT MINERAL SUNSCREEN WITH CLEAR ZINC, (uncoated 25% zinc by The W.S. Badger Company, Inc.. Reason: Labeling: Missing Label: The finished product potentially missing the labeling with the drug facts panel, bar code and directions for use..
Details
Source
Drug Recall
External ID
D-0209-2025
Action Date
2025-02-05
Status
Terminated
Category
drug
Product Description
BADGER 50, ADVENTURE SPORT MINERAL SUNSCREEN WITH CLEAR ZINC, (uncoated 25% zinc oxide), 2.4 oz., Tin, W.S. Badger Company, Inc, 768 Route 10, Gilsum NH, 03448 UPC 6 34084 47150 2
Lot/Code Info: LOT# 091923A, Exp. Date 09/19/26
Quantity Affected: 4,834 tins
Reason for Recall
Labeling: Missing Label: The finished product potentially missing the labeling with the drug facts panel, bar code and directions for use.
Distribution
Distributed Nationwide in the USA
Type: Voluntary: Firm initiated
Recall Initiated: 2025-01-17
Company
Gilsum, NH
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 45 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
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 (The W.S. Badger Company, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does The W.S. Badger Company, Inc. have FDA actions?
This is the only FDA action we have on record for The W.S. Badger Company, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0209-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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