Dynarex Corporation Recalls

6 recalls found for Dynarex Corporation. Check if any of your products are affected.

HIGHFDA DRUG

Dynarex Obstetrical Towelettes Cleanser Recall 2026 for CGMP Deviations

Dynarex Obstetrical Towelettes Cleanser is under an active FDA recall as of Jan. 20, 2026. The recall cites CGMP Deviations that could affect product quality. Consumers and healthcare providers should stop using the product immediately and contact ACME United Corporation or a healthcare provider for guidance.

BZK PADS
CGMP Deviations
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HIGHFDA DRUG

Dynarex Recalls Wecare Enema Due to Safety Violations

Dynarex Corporation recalled 18,912 containers of Wecare Enema on October 31, 2025, due to cGMP deviations. Consumers should stop using the product immediately. The recall affects products distributed nationwide in the USA.

SALINE ENEMA
cGMP deviations
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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.

DYNASHIELD
cGMP deviations
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HIGHFDA DRUG

Dynashield Skin Protectant Recalled for cGMP Violations

Dyrnarex Corporation recalled 1,560 containers of Dynashield Skin Protectant on October 31, 2025. The product may not meet current Good Manufacturing Practice standards. Consumers should stop using the product immediately and seek guidance from healthcare providers.

DYNASHIELD
cGMP deviations
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HIGHFDA DRUG

Dynarex Recalls Wecare Calasoothe Ointment Over cGMP Violations

Dynarex Corporation recalled 2,400 containers of Wecare Calasoothe on October 31, 2025, due to cGMP deviations. The recall affects the 4 oz ointment, as it may not meet safety standards. Consumers should stop using the product immediately and consult their healthcare providers.

MENTHOL AND ZINC OXIDE
cGMP deviations
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HIGHFDA DRUG

Dynarex Recalls Zinc Oxide Ointment Over cGMP Deviations

Dynarex Corporation recalled 2,592 bottles of WeCare Zinc Oxide Ointment on October 31, 2025, due to cGMP deviations. The recall affects products distributed nationwide in the USA. Consumers and healthcare providers must stop using the ointment immediately and seek guidance.

ZINC OXIDE
cGMP deviations
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Brand Statistics

Total Recalls
6
Pages
1