Ultra Seal Corporation recalls MAGNAC: calcium carbonate tablets due to manufacturing quality control issues. Affected lots produced for Afassco Inc. in Minden, NV. No specific remedy stated in recall notice.
cGMP deviations
Ultra Seal Corporation is recalling MAGNACAL calcium carbonate tablets because of manufacturing quality control issues. This recall affects specific lots produced for Afassco Inc. in Minden, NV. The issue does not involve immediate safety risks but requires consumers to check their product details.
The recall is due to cGMP (current Good Manufacturing Practice) deviations, which means the tablets were made under quality control standards that did not meet regulatory requirements. This could affect the product's safety and effectiveness, but the recall does not indicate immediate health risks.
People who own or use MAGNACAL calcium carbonate tablets manufactured for Afassco Inc. in Minden, NV. Those with the specific lot number AK9768 (expiring 08/2022) are most at risk.
Check for the product name MAGNACAL (calcium carbonate 420 mg) in 2 tablet packets. Look for the lot number AK9768 with an expiration date of 08/2022 on the packaging.
Verify the product name, lot number, and expiration date on the packaging to confirm if it matches the recalled items.
The recall is due to manufacturing quality control issues, not immediate safety risks. The product is not considered dangerous for normal use.
The recall notice does not specify a remedy, so no action is required beyond checking the product details.
Check for the lot number AK9768 with an expiration date of 08/2022 on the MAGNACAL (calcium carbonate 420 mg) 2 tablet packets.
We’ve drafted a message you can send Ultra Seal to request your refund or repair — edit it as you like.
Subject: Recall D-0500-2022 — Ultra Seal Ultra Seal Hello, I own a Ultra Seal that is covered by recall D-0500-2022 from Ultra Seal. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
