HIGHFDA DRUG

CA Botana Doctor D. Schwab Shimmery Sun Lotion Sunscreen Recall for CGMP Deviations (2025)

CA Botana International recalled 805 tubes of Doctor D. Schwab Shimmery Sun Lotion Sunscreen SPF 30 after CGMP deviations were identified. The recall covers tubes sold in California, Colorado, Florida, Puerto Rico, and Washington. Consumers should stop using the product immediately and contact the company for guidance.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
October 10, 2025
Status
ACTIVE
Severity
8/10

Quick Facts at a Glance

Recall Date
October 10, 2025
Hazard Level
HIGH
Brands
Doctor D. Schwab, CA-BOTANA INTERNATIONAL
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
5 states
At-Risk Groups
GENERAL, PREGNANT, PETS

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Doctor D. Schwab, CA-BOTANA INTERNATIONAL
Product type
Sunscreen Lotion
Model numbers
Lot D54597, exp 1/31/2028
UPC codes
35192-012, 35192-012-02
Sold at
Multiple Retailers
Where affected
CA, CO, FL, PR, WA

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    October 10, 2025

  2. Reported by FDA DRUG

    December 3, 2025

  3. RecallRadar source check

    April 18, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

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

About This Product

Shimmery Sun Lotion Sunscreen SPF 30 is a cosmetic sunscreen product sold in tubes. Consumers use it to protect skin from sun exposure.

Why This Is Dangerous

CGMP deviations indicate manufacturing quality concerns. No direct chemical hazard is listed in the notice, but quality deviations can affect product safety.

Industry Context

This recall is not identified as part of a broader pattern in this document.

Real-World Impact

Immediate stop-use is advised. No injuries reported yet. Consumers should await guidance from CA BOTANA for refunds or replacements.

Practical Guidance

How to identify if yours is affected

  1. Check tube for Lot D54597
  2. Check expiry date 01/31/2028
  3. Verify NDC 35192-012-02 on packaging

Where to find product info

FDA enforcement page and CA BOTANA recall notice for specifics

What timeline to expect

Refunds or replacements are communicated by mailed notification; processing times not specified

If the manufacturer is unresponsive

  • Document all correspondence
  • File a complaint with FDA/FTC if company delays
  • Consider legal counsel for unresponsive manufacturers

How to prevent similar issues

  • Purchase from reputable retailers
  • Verify CGMP compliance during production
  • Keep receipts and packaging for recalls
  • Monitor FDA recall notices for cosmetic products

Documentation advice

Keep product, photos of label and lot code, and all correspondence

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Product Details

Brand: Doctor D. Schwab. Product: Shimmery Sun Lotion Sunscreen SPF 30. Net weight: 4 oz. per tube. Lot: D54597. Expiration: 01/31/2028. NDC: 35192-012-02. Quantity: 805 tubes. Distribution: CA, CO, FL, PR, WA. Sold by: CA BOTANA International, Inc. (A division of CA BOTANA). Recall date: 2025-10-10. Status: ACTIVE.

Reported Incidents

No injuries or incidents have been reported in the provided document.

Key Facts

  • Sold in CA, CO, FL, PR, WA

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERALPREGNANTPETS
Injury Types
POISONINGBURNOTHER

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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