GM Manufacturing recalls Calcium Formula 250 cc HDPE bottles due to cGMP regulatory violations in dietary supplements. Affected products were sold with expiration date 08.2016.
GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
GM Manufacturing is recalling Calcium Formula dietary supplements in 250 cc HDPE bottles because they violated food safety regulations. This recall affects products sold with an expiration date of August 2016.
The recall is due to significant violations of current Good Manufacturing Practices (cGMP) regulations for dietary supplements. These violations could lead to unsafe product quality, but the specific hazard mechanism isn't clearly described in the notice.
People who purchased Calcium Formula dietary supplements in 250 cc HDPE bottles with an expiration date of August 2016 are affected. Those using these supplements for medical purposes may be at higher risk due to potential contamination.
Check for Calcium Formula dietary supplements in 250 cc HDPE bottles with an expiration date of August 2016. The product name and expiration date are listed on the bottle.
Look for the product name 'Calcium Formula', 250 cc HDPE bottles, and expiration date 08.2016 on the bottle.
The recall is due to significant violations of current Good Manufacturing Practices (cGMP) regulations for dietary supplements.
The recall notice does not specify a remedy or action to take for affected products.
The recall notice does not describe a specific hazard mechanism that could cause injury.
We’ve drafted a message you can send GM Manufacturing to request your refund or repair — edit it as you like.
Subject: Recall F-2256-2014 — GM Manufacturing GM Manufacturing Hello, I own a GM Manufacturing that is covered by recall F-2256-2014 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.
