GM Manufacturing recalls Therapeutic Care A, B, C dietary supplements for cGMP regulatory violations. Products sold with specific lot numbers from November 2016.
GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
GM Manufacturing is recalling Therapeutic Care A, B, and C dietary supplements because they violated food safety regulations. This recall affects products with specific lot numbers from November 2016.
The products were found to have significant violations of current Good Manufacturing Practices (cGMP) regulations for dietary supplements. This means the supplements may not be safe or effective as intended, potentially causing health risks.
Dietary supplement users who purchased Therapeutic Care A, B, or C products with the listed lot numbers from November 2016 are affected. People using these supplements for medical purposes may be at higher risk due to regulatory violations.
Check the product label for lot numbers KZ1350, KZ1351, or KZ1352 with expiration dates of November 2016. These products were sold as Therapeutic Care A, B, or C dietary supplements.
Look for lot numbers KZ1350, KZ1351, or KZ1352 with expiration dates of November 2016 on the product label.
GM Manufacturing is recalling these products due to significant violations of cGMP regulations for dietary supplements.
Therapeutic Care A, B, and C dietary supplements with lot numbers KZ1350, KZ1351, or KZ1352 that expired in November 2016.
Check the product label for lot numbers KZ1350, KZ1351, or KZ1352 with an expiration date of November 2016.
We’ve drafted a message you can send GM Manufacturing to request your refund or repair — edit it as you like.
Subject: Recall F-2268-2014 — GM Manufacturing GM Manufacturing Hello, I own a GM Manufacturing that is covered by recall F-2268-2014 from GM Manufacturing. 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.
