ULTRAtab Laboratories recalls Zee Cold Tabs due to CGMP deviations. This may affect safety but no specific harm is confirmed. Check NDC 62959-111-xx for affected units.
CGMP Deviations
ULTRAtab Laboratories is recalling Zee Cold Tabs (Acetaminophen 325 mg, Guaifenesin 100 mg, Phenylephrine HCl 5 mg) because of CGMP deviations. This recall does not indicate a specific safety risk or harm to consumers.
CGMP deviations refer to failures in manufacturing quality control. This could mean the product does not meet safety standards, but the recall does not specify how this affects the product's safety or health.
Anyone who owns or uses Zee Cold Tabs with NDC 62959-111-xx. People taking cold medications are most at risk if they have the recalled product.
Check for NDC code 62959-111-xx on the product label. The product is a bulk container from ULTRAtab Laboratories, Inc. in Highland, NY.
Look for NDC code 62959-111-xx on the Zee Cold Tabs container.
The recall mentions CGMP deviations but does not specify any risk of serious injury or harm.
Check for NDC code 62959-111-xx on the product label. The product is a bulk container from ULTRAtab Laboratories, Inc. in Highland, NY.
The recall does not provide specific action steps for consumers beyond checking the product label.
We’ve drafted a message you can send ULTRAtab Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-0525-2022 — ULTRAtab Laboratories ULTRAtab Laboratories Hello, I own a ULTRAtab Laboratories that is covered by recall D-0525-2022 from ULTRAtab Laboratories. 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.
