Encon Safety Products recalls AQ 120 GFEW Aquarion Preserved Cartridges sold nationwide through multiple retailers. The recall cites cGMP deviations in manufacturing. Stop using the product immediately and follow recall guidance from Encon Safety or your healthcare provider.
cGMP deviations.
Consumers and healthcare providers should stop using this product immediately. Contact Encon Safety Products Co or your healthcare provider for guidance. Notification method: Letter
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AQ 120 GFEW Aquarion Preserved Cartridges are distributed nationwide and tied to healthcare or related settings. The recall covers 7677 bags and multiple model lots with varying expiration dates.
cGMP deviations refer to manufacturing practices not meeting current GMP standards. This raises questions about product quality and consistency, which could affect safety and efficacy.
This recall is not described as part of a broader industry pattern.
Consumers and facilities should halt use immediately. The impact is primarily potential quality concerns rather than documented harm at this time; active recall suggests a precautionary approach and potential disruption to workflows.
FDA recall page and enforcement report D-0260-2026 linked in the notice.
Remedy processing guidance is not specified; refunds or replacements, if provided, typically take 4-8 weeks after submission.
Keep packaging, recall notices, and correspondence. Photograph the lot number and expiration date for records.
Model numbers and lot information are listed below. Distribution was nationwide within the United States.
Not sure what to do next? Our guide walks you through the process step by step.
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