HIGH

Karina Daily Moisturizer Recalled Over CGMP Deviations

Beauty4Pros LLC recalled 1,492 tubes of Karina Daily Moisturizer SPF 25 on October 10, 2025. The recall follows concerns regarding current good manufacturing practice (CGMP) deviations. Affected products were distributed in California, Colorado, Florida, Puerto Rico, and Washington.

Quick Facts at a Glance

Recall Date
October 10, 2025
Hazard Level
HIGH
Brands
SUNSCREEN KARINA SKIN CARE MOIST, 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 recalled product is Karina Daily Moisturizer SPF 25, containing Octinoxate 7.5% and Zinc Oxide 7.0%. It has a net weight of 5 oz (141.7 g) per tube. The recall affects lot number D54098, set to expire on March 31, 2027.

The Hazard

The recall stems from deviations related to current good manufacturing practices (CGMP). These issues can potentially compromise the product's safety and efficacy.

Reported Incidents

No specific incidents of injury or illness have been reported in connection with this recall. The absence of reported injuries does not negate the potential risks associated with CGMP deviations.

What to Do

Consumers should stop using the product immediately. Contact CA BOTANA International, Inc. or your healthcare provider for further guidance.

Contact Information

For more information, visit the FDA recall page at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=D-0191-2026.

Key Facts

  • Recall Date: October 10, 2025
  • Quantity Recalled: 1,492 tubes
  • Affected States: CA, CO, FL, PR, WA
  • NDC: 35192-033-16
  • UPC: 8 18204 02572 5

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Safety Assessment

Risk LevelHIGH
Severity Score
7/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
Lot D54098
exp 3/31/2027
UPC Codes
35192-033
35192-033-16
Affected States
CA, CO, FL, PR, WA
Report Date
December 3, 2025
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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