CLASS III Drug recall · Reported 5 Feb 2025 · FDA Enforcement Report
Badger 50, Adventure Sport Mineral Sunscreen With Clear recalled
The W.S. Badger is recalling Badger 50, Adventure Sport Mineral Sunscreen With Clear Zinc, (uncoated 25% zinc oxide), distributed nationwide in the US. The recall was initiated on 17 Jan 2025 and the FDA has classified it as Class III.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0209-2025
- FDA event ID
- 96122
- Recalling firm
- The W.S. Badger, Gilsum, NH
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 17 Jan 2025
- FDA classified
- 29 Jan 2025
- Reported
- 5 Feb 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Labeling Errors
- Drug class
- Sunscreen & Personal Care
Timeline
| 17 Jan 2025 | Recall initiated by company | |
| 29 Jan 2025 | Classified by FDA | +12 days |
| 5 Feb 2025 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Labeling: Missing Label: The finished product potentially missing the labeling with the drug facts panel, bar code and directions for use.
Product as listed by the FDA
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
Where it was distributed
Distributed Nationwide in the USA
Questions about this recall
Why was it recalled?
Labeling: Missing Label: The finished product potentially missing the labeling with the drug facts panel, bar code and directions for use.
Which lots are affected?
LOT# 091923A, Exp. Date 09/19/26
Where was it sold?
Distributed Nationwide in the USA
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.