HIGH

Dynashield Cream Recalled Due to cGMP Deviations

Dynashield, a 4 oz cream, is recalled after cGMP deviations were identified. The recall affects 7,944 units distributed nationwide. Consumers should stop using the product immediately and contact their healthcare provider for guidance.

Quick Facts at a Glance

Recall Date
October 31, 2025
Hazard Level
HIGH
Brands
DYNASHIELD, Dynarex Corporation
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

Dynashield cream, 4 oz (113 g), manufactured for Dynarex Corporation. Lot numbers include A092421, A092340, A092346. Distributed nationwide in the USA.

The Hazard

The cream has been found to have deviations from current Good Manufacturing Practices (cGMP). Such issues may affect the product's safety and efficacy.

Reported Incidents

No specific injuries or incidents have been reported at this time. The recall is precautionary due to manufacturing deviations.

What to Do

Stop using Dynashield cream immediately. Contact Blossom Pharmaceuticals or your healthcare provider for further guidance. Notification will be sent via letter.

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-0207-2026.

Key Facts

  • Recalled product: Dynashield cream, 4 oz
  • Recall date: October 31, 2025
  • Quantity recalled: 7,944 containers
  • Reason: cGMP deviations
  • Manufactured in India

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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 #: A092421
Exp. Date 7/27
A092340
Exp. Date 10/26 & A092346
Exp. Date 11/26.
UPC Codes
67777-407
67777-407-01
67777-407-02
+4 more
Affected States
ALL
Report Date
December 10, 2025
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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