Hi-Tech Pharmacal recalls Rx CHOICE Liquid Vitamin C (16 fl oz) due to out-of-specification pH levels. Consumers should check product lot numbers and contact the company for details.
Out-of-specification results for pH.
Hi-Tech Pharmacal is recalling Rx CHOICE Liquid Vitamin C (16 fl oz) because the product's pH levels are outside acceptable specifications. This could affect the product's safety and effectiveness, though the recall does not indicate immediate health risks.
The product's pH levels are outside the specified range, which could impact the product's stability and effectiveness. However, the recall does not indicate that the product poses an immediate health risk or safety hazard.
Owners of Rx CHOICE Liquid Vitamin C (16 fl oz) with lot numbers 618283 through 627676 are affected. People using this product for general health purposes may be at risk if the pH levels are not within safe limits.
Check the product label for the lot number: 618283 (expires 01/2015), 620151 (expires 03/2015), 623407 (expires 09/2015), or extension lots 620915 through 627676 (with corresponding expiration dates).
Look for the lot number on the label: 618283, 620151, 623407, or extension lots 620915 through 627676.
The recall indicates the product's pH levels are out of specification, but the official notice does not state that it poses an immediate health risk or safety hazard.
Check the product lot number. If it matches the recalled lots, contact Hi-Tech Pharmacal for further instructions.
Check the product label for the lot number: 618283 (expires 01/2015), 620151 (expires 03/2015), 623407 (expires 09/2015), or extension lots 620915 through 627676 (with corresponding expiration dates).
We’ve drafted a message you can send Hi-Tech Pharmacal to request your refund or repair — edit it as you like.
Subject: Recall F-0817-2017 — Hi-Tech Pharmacal Hi-Tech Pharmacal Hello, I own a Hi-Tech Pharmacal that is covered by recall F-0817-2017 from Hi-Tech Pharmacal. 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.
