HIGH

Doctor D. Schwab Sunscreen Recalled Due to CGMP Deviations

Doctor D. Schwab recalled 805 tubes of Shimmery Sun Lotion Sunscreen SPF 30 on October 10, 2025. The recall follows significant deviations from current good manufacturing practices (CGMP). Consumers should stop using the product immediately and contact CA BOTANA for guidance.

Quick Facts at a Glance

Recall Date
October 10, 2025
Hazard Level
HIGH
Brands
SHIMMERY SUN, CA-BOTANA INTERNATIONAL
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
5 states
At-Risk Groups
GENERAL

Hazard Information

CGMP Deviations

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact CA BOTANA International, Inc. or your healthcare provider for guidance. Notification method: Letter

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Product Details

The sunscreen is sold in 4 oz. (113.4 g) tubes. The affected model is Lot D54597, which expires on January 31, 2028. The product is distributed in California, Colorado, Florida, Puerto Rico, and Washington.

The Hazard

This product has been recalled due to CGMP deviations, which can lead to potential safety issues. CGMP deviations can affect the quality and safety of the product, posing a risk to consumers.

Reported Incidents

No specific incidents or injuries have been reported associated with this recall. Consumers are advised to take the recall seriously due to the high hazard level.

What to Do

Stop using the product immediately. Contact CA BOTANA International, Inc. or your healthcare provider for further guidance. Notification has been sent via letter.

Contact Information

For more information, call CA BOTANA International, Inc. or visit their website at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=D-0189-2026.

Key Facts

  • 805 tubes recalled
  • SPF 30 with Titanium Dioxide and Octinoxate
  • Stop using immediately
  • High hazard level

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
Lot D54597
exp 1/31/2028
UPC Codes
35192-012
35192-012-02
Affected States
CA, CO, FL, PR, WA
Report Date
December 3, 2025
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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