Lupin Pharmaceuticals recalls GaviLyte -C oral solution with failed stability specification. This may affect safety and requires checking product details.
Failed Stability Specification
Lupin Pharmaceuticals is recalling GaviLyte -C oral solution due to a failed stability specification. This means the product may not be safe for use as intended.
The product failed stability specifications, which means it may not be safe for use. This could lead to potential safety issues if the solution is not properly stored or handled.
People who own or use GaviLyte -C oral solution with NDC# 43386-060-19 and lot number S001132, expiring July 2022 are affected. Those with the product are most at risk.
Check for NDC# 43386-060-19 and lot number S001132 on the product label. The expiration date is July 2022.
Look for NDC# 43386-060-19 and lot number S001132 on the product label.
The recall states the product failed stability specifications, but does not specify if it is safe to use. The official notice does not provide details on whether the product is safe.
The recall does not specify any action steps for affected products. The official notice does not provide a remedy.
Check for NDC# 43386-060-19 and lot number S001132 on the product label. The expiration date is July 2022.
We’ve drafted a message you can send Lupin Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0875-2022 — Lupin Pharmaceuticals Lupin Pharmaceuticals Hello, I own a Lupin Pharmaceuticals that is covered by recall D-0875-2022 from Lupin Pharmaceuticals. 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.
