Safecor Health recalls vitamin D oral syringes that may leak after repackaging. Stop using if you have the specific lot numbers listed. No immediate injury risk but leakage could cause contamination.
Defective Delivery System: Leakage observed after oral solution was repackaged into unit-dose syringes.
Safecor Health is recalling vitamin D supplements in 0.05 mL oral syringes due to leakage after repackaging. This could lead to contamination of the solution if the syringe leaks. The recall does not involve immediate injury risks but requires stopping use to prevent potential contamination.
The syringes may leak after being repackaged, which could cause the vitamin D solution to contaminate other surfaces or materials. This leakage risk is not immediate but could lead to unintended exposure if the syringe is not properly sealed.
People who own the specific vitamin D syringes with lot numbers 24300812 (expires Jan 2025) or 24530836 (expires July 2025) are affected. Those using the product for medical purposes are most at risk due to potential contamination.
Check for lot numbers 24300812 (expires Jan 2025) or 24530836 (expires July 2025) on the packaging. The product is a vitamin D supplement in 0.05 mL oral syringes.
Discard the syringe if you have the affected lot numbers to prevent potential contamination.
Yes, if you have the specific lot numbers listed in the recall, you should stop using and discard the syringe to prevent potential contamination.
The recall states that leakage may occur after repackaging, which could lead to contamination of surfaces or materials. However, no injuries have been reported.
Check the lot number on the packaging; affected units have lot numbers 24300812 (expires Jan 2025) or 24530836 (expires July 2025).
We’ve drafted a message you can send Safecor Health to request your refund or repair — edit it as you like.
Subject: Recall D-0250-2025 — Safecor Health Safecor Health Hello, I own a Safecor Health that is covered by recall D-0250-2025 from Safecor Health. 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.
