HIGHFDA DRUG

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.

Official notice
Blossom PharmaceuticalsHealth & Personal CareDrugs & MedicationsLot #: A322301Exp. Date 7/26 & A322302Exp. Date 8/26

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
8/10

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

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
Blossom Pharmaceuticals
Product type
Moisturizing Wound Hydrogel
Model numbers
Lot #: A322301, Exp. Date 7/26 & A322302, Exp. Date 8/26
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

Dynagel Moisturizing Wound Hydrogel is designed to provide hydration to wounds and promote healing. Consumers typically use it for minor cuts, abrasions, and skin irritations.

Why This Is Dangerous

The product's cGMP deviations can lead to contamination or reduced effectiveness, compromising consumer safety during use.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

The recall affects consumers by necessitating immediate discontinuation of use, with potential safety concerns until the issue is resolved.

Practical Guidance

How to identify if yours is affected

  1. Check the product label for lot numbers A322301 and A322302.
  2. Verify the expiration dates: July 2026 and August 2026.
  3. If your product matches the recalled lot numbers, cease use immediately.

Where to find product info

The lot numbers and expiration dates can be found on the product packaging.

What timeline to expect

Expect a processing timeline of approximately 4-6 weeks for refunds or replacements.

If the manufacturer is unresponsive

  • Document your communication attempts with the company.
  • Consider following up with your healthcare provider for advice on alternatives.

How to prevent similar issues

  • Look for products with a clear cGMP certification.
  • Check for recent recalls on similar products from reputable sources.
  • Consult healthcare providers for recommended wound care products.

Documentation advice

Keep records of your purchase, any correspondence related to the recall, and photos of the product.

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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.

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

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
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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