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Health Alerts

Your unified view of current, active outbreak investigations, elevated disease activity, and food and drug recalls -- reported directly by CDC, FDA, and USDA. Not CDC NORS, which is a historical archive compiled well after an investigation closes (see Data Explorer for the full historical record).

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Showing 201–220 of 224 alerts

Food Recall 2026 record Source: FDA

D'Dioses Fruit Pops, Inc.

Recall initiated
May 4, 2026
Reported by FDA
July 22, 2026

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Food Recall 2026 record Source: FDA

D'Dioses Fruit Pops, Inc.

Recall initiated
May 4, 2026
Reported by FDA
July 22, 2026

View Details

Food Recall 2026 record Source: FDA

D'Dioses Fruit Pops, Inc.

Recall initiated
May 4, 2026
Reported by FDA
July 22, 2026

View Details

Food Recall 2026 record Source: FDA

D'Dioses Fruit Pops, Inc.

Recall initiated
May 4, 2026
Reported by FDA
July 22, 2026

View Details

Food Recall 2026 record Source: FDA

D'Dioses Fruit Pops, Inc.

Recall initiated
May 4, 2026
Reported by FDA
July 22, 2026

View Details

Food Recall 2026 record Source: FDA

D'Dioses Fruit Pops, Inc.

Recall initiated
May 4, 2026
Reported by FDA
July 22, 2026

View Details

Food Recall 2026 record Source: FDA

D'Dioses Fruit Pops, Inc.

Recall initiated
May 4, 2026
Reported by FDA
July 22, 2026

View Details

Food Recall 2026 record Source: FDA

D'Dioses Fruit Pops, Inc.

Recall initiated
May 4, 2026
Reported by FDA
July 22, 2026

View Details

Food Recall 2026 record Source: FDA

D'Dioses Fruit Pops, Inc.

Recall initiated
May 4, 2026
Reported by FDA
July 22, 2026

View Details

Food Recall 2026 record Source: FDA

D'Dioses Fruit Pops, Inc.

Recall initiated
May 4, 2026
Reported by FDA
July 22, 2026

View Details

Food Recall 2026 record Source: FDA

D'Dioses Fruit Pops, Inc.

Recall initiated
May 4, 2026
Reported by FDA
July 22, 2026

View Details

Food Recall 2026 record Source: FDA

D'Dioses Fruit Pops, Inc.

Recall initiated
May 4, 2026
Reported by FDA
July 22, 2026

View Details

Food Recall 2026 record Source: FDA

D'Dioses Fruit Pops, Inc.

Recall initiated
May 4, 2026
Reported by FDA
July 22, 2026

View Details

Drug Recall 2026 record Source: FDA

Revitaderm Wound Care, First Aid Antiseptic Gel, Benzalkonium Chloride 0.1%) packaged as (a) 1.0 Fl OZ (16 mL) bottle, long pointy cap, NDC 63347-120-02; (b) 3.0 Fl OZ (85 g) tube, with short twist cap, NDC 63347-120-01; Manufactured By: Blaine Labs, Inc. 11037 Lockport Place, Santa Fe Springs, CA 90670,

Recall initiated
April 8, 2026
Reported by FDA
July 8, 2026

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Drug Recall 2026 record Source: FDA

Fungal Fusion ERADICATION Solution, Antifungal & Antimicrobial Kit. Contains, 1x2 oz bottle Fungal Fusion Antifungal (Miconazole Nitrate) Cream, 1x2oz bottle Fungal Fusion Antifungal Solution (25% Undecylenic Acid) and 1x1oz bottle of Fungal Fusion Eradication Antimicrobial Show Spray (isopropyl Alcohol, D-Limonene, Undecylenic Acid). Manufactured By: Blaine Labs, Inc., 11037 Lockport Place, Santa Fe Springs, CA 90670, Manufactured for Doctor's Inc

Recall initiated
April 8, 2026
Reported by FDA
July 8, 2026

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Drug Recall 2026 record Source: FDA

TERPENICOL Antifungal Solution, (Undecylenic (10-Undecenoic) acid 25%), 1.0 Fl Oz (29.6 mL), Manufactured By: Blaine Labs, Inc., 11037 Lockport Place, Santa Fe Springs, CA 90670. NDC 63347-600-01

Recall initiated
April 8, 2026
Reported by FDA
July 8, 2026

View Details

Drug Recall 2026 record Source: FDA

vite20 Antifungal Cream, (10% Undecylenic Acid), 0.54 OZ (15 g) bottle, Manufactured By: Blaine Labs, Inc., 11037 Lockport Place, Sante Fe Springs, CA 90670, UPC 6 16728 00039 2.

Recall initiated
April 8, 2026
Reported by FDA
July 8, 2026

View Details

Drug Recall 2026 record Source: FDA

TERPENICOL Antifungal Cream (Undecylenic Acid 13%), 1.0 oz (28 g) bottles, Manufactured By: Blaine Labs, Inc., 11037 Lockport Place, Sante Fe Springs, CA 90670, NDC 63347-601-01.

Recall initiated
April 8, 2026
Reported by FDA
July 8, 2026

View Details

Drug Recall 2026 record Source: FDA

TRIPENICOL S Antifungal Solution (Undecylenic Acid 25%), 1.25 FL OZ (37.5 mL) bottle, Manufactured For: Trifluent Pharma, LLC, San Antonio, TX 78213, NDC 73352-550-01.

Recall initiated
April 8, 2026
Reported by FDA
July 8, 2026

View Details

Drug Recall 2026 record Source: FDA

TRIFLUENT PHARMA TRIDERGEL Wound Care Gel, (Benzalkonium Chloride 0.1%), 1.0 fl oz, (29.6 mL) bottle with long pointy cap, Manufactured for: Trifluent Pharma, LLC. San Antonio, TX 78213. NDC 73352-520-01.

Recall initiated
April 8, 2026
Reported by FDA
July 8, 2026

View Details

Data last updated:

Investigations and recalls may be ongoing; status, case counts, and guidance are updated by the source agency as events continue. Read the full medical disclaimer.

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