HIGHFDA DRUG

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.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
October 31, 2025
Status
ACTIVE
Severity
7/10

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

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
DYNASHIELD, Dynarex Corporation
Product type
Cream
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, 67777-407-03, 67777-407-10, 67777-407-04, 67777-407-11
Sold at
Multiple Retailers
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    October 31, 2025

  2. Reported by FDA DRUG

    December 10, 2025

  3. RecallRadar source check

    December 17, 2025

  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 Blossom Pharmaceuticals or your healthcare provider for guidance. Notification method: Letter

About This Product

Dynashield cream is a topical product primarily used as a skin protectant containing zinc oxide. Consumers typically buy it for wound care, diaper rash prevention, and to soothe irritated skin.

Why This Is Dangerous

cGMP deviations indicate that the manufacturing process may have failed to meet necessary quality standards, potentially leading to contamination or ineffective products.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers may face inconvenience due to the need to stop using the product and seek alternatives, but there are no immediate health risks reported.

Practical Guidance

How to identify if yours is affected

  1. Check the product packaging for lot numbers A092421, A092340, or A092346.
  2. Verify the expiration date against the recall information.
  3. Determine where the product was purchased to contact the retailer if needed.

Where to find product info

Lot numbers and expiration dates can usually be found on the back or bottom of the product container.

What timeline to expect

Refund processing may take 4-6 weeks depending on the company's procedures.

If the manufacturer is unresponsive

  • Contact the retailer where the product was purchased.
  • Reach out to Blossom Pharmaceuticals directly for further assistance.

How to prevent similar issues

  • Look for products with clear cGMP certifications in the future.
  • Research brand reputation before purchasing personal care products.
  • Read customer reviews for safety concerns.

Documentation advice

Keep all correspondence, receipts, and any related documentation until the refund process is complete.

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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.

Key Facts

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

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
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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