Specialty Process Labs recalls thyroid medication for manufacturing use due to failed stability specifications. This product may not be safe for intended purpose.
Failed Stability Specifications
Specialty Process Labs is recalling thyroid medication intended for manufacturing and repackaging. The product failed stability tests, meaning it might not be safe for its intended use.
The medication failed stability specifications, meaning it may not maintain its intended properties over time. This could affect its safety and effectiveness for manufacturing and repackaging purposes.
Manufacturers and repackagers using this thyroid medication for processing. Those handling the product in manufacturing settings are most at risk.
Look for the product name 'S.P.Labs Thyroid, Full Strength' with NDC 81305-500-01. Check for lot number H22212-FSV and expiration date 11/21/2024.
Verify the product name, NDC number, lot number, and expiration date to confirm if it matches the recalled items.
No, this product is intended for manufacturing and repackaging use only, not for human consumption.
The recall does not specify a remedy, so check with the manufacturer for guidance.
The recall states failed stability specifications, which could affect safety for manufacturing use, but no specific injury risk is mentioned.
We’ve drafted a message you can send S.P.Labs to request your refund or repair — edit it as you like.
Subject: Recall D-0446-2024 — S.P.Labs S.P.Labs Hello, I own a S.P.Labs that is covered by recall D-0446-2024 from S.P.Labs. 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.
