Novacare is recalling 120-count glucosamine capsules due to inadequate allergen labeling. Consumers should check lot numbers 4102801, 2071918.2, 2061401, and 2032006 for affected products.
TSN Labs is conducting a field action on Glucosamine 750 mg 120 ct due to inadequate allergen labeling.
Novacare is recalling 120-count glucosamine capsules because they lack proper allergen labeling. This could pose a risk for people with allergies to ingredients like shellfish, as the labeling doesn't clearly identify potential allergens.
The capsules lack clear allergen labeling, which means consumers might not know if they have an allergy to ingredients like shellfish. This could lead to allergic reactions if someone takes the product without knowing the allergen content.
People who own or use Novacare's 120-count glucosamine capsules with lot numbers 4102801, 2071918.2, 2061401, or 2032006 are affected. Those with shellfish allergies or other allergens listed on the product may be at higher risk.
Check the lot number on the product packaging. Affected lots are 4102801, 2071918.2, 2061401, and 2032006. The product is a 120-count glucosamine capsule with a dosage of 1.5 capsules three times daily.
Look for the lot numbers 4102801, 2071918.2, 2061401, or 2032006 on the packaging.
The product lacks adequate allergen labeling, which could pose a risk for people with allergies to ingredients like shellfish.
Lot numbers 4102801, 2071918.2, 2061401, and 2032006 are affected.
No, but you should check the lot number to ensure you have an affected product. If you do, contact Novacare for further instructions.
We’ve drafted a message you can send Novacare to request your refund or repair — edit it as you like.
Subject: Recall F-2946-2015 — Novacare Novacare Hello, I own a Novacare that is covered by recall F-2946-2015 from Novacare. 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.
