HIGH

Dynarex Recalls Moisturizing Wound Hydrogel Over cGMP Violations

Dynarex Corporation recalled 8,184 bottles of Dynagel Moisturizing Wound Hydrogel on October 31, 2025. The recall follows deviations from current Good Manufacturing Practices (cGMP). Consumers should stop using the product immediately and consult healthcare providers for guidance.

Quick Facts at a Glance

Recall Date
October 31, 2025
Hazard Level
HIGH
Brand
Blossom Pharmaceuticals
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

cGMP deviations

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact Blossom Pharmaceuticals or your healthcare provider for guidance. Notification method: Letter

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Product Details

The recalled product is Dynagel Moisturizing Wound Hydrogel, net weight 3oz (84.7 g). It is identified by UPC 61784128016 and includes lot numbers A322301 with an expiration date of July 2026 and A322302 with an expiration date of August 2026. The product was distributed nationwide in the USA.

The Hazard

The recall stems from deviations from current Good Manufacturing Practices (cGMP). These violations can lead to potential safety risks, including contamination or ineffective treatment.

Reported Incidents

No specific incidents or injuries have been reported related to this recall as of the latest report date, December 10, 2025.

What to Do

Consumers and healthcare providers should stop using the product immediately. Contact Blossom Pharmaceuticals or consult with a healthcare provider for guidance on disposal and potential alternatives.

Contact Information

For further information, consumers can visit the FDA website at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=D-0204-2026.

Key Facts

  • Recall date: October 31, 2025
  • Reported date: December 10, 2025
  • Total quantity recalled: 8,184 bottles
  • Lot numbers: A322301, A322302
  • Exp. dates: July 2026, August 2026

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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 #: A322301
Exp. Date 7/26 & A322302
Exp. Date 8/26
Affected States
ALL
Report Date
December 10, 2025
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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