Safecor Health recalls iron supplement syringes that may leak after repackaging, causing potential contamination. Affected products include specific NDC numbers and expiration dates.
Defective Delivery System: Leakage observed after oral solution was repackaged into unit-dose syringes.
Safecor Health is recalling iron supplement syringes that may leak after being repackaged into unit-dose syringes. This leakage could lead to contamination of the iron supplement solution, posing a risk of improper dosing or exposure to harmful substances.
The syringes may leak after the oral solution is repackaged into unit-dose syringes. This leakage could cause the iron supplement to mix with other substances, potentially leading to improper dosing or contamination.
People who purchased the affected iron supplement syringes from Safecor Health in Columbus, Ohio. Those most at risk are individuals using the product for iron supplementation who may have experienced leakage.
Check for the product names: Ferrous Sulfate 7.5 mg Iron/0.5 mL Oral Syringe, Delivers: 0.5 mL, Iron Supplement Drops. The NDC numbers are 71399748005, 39328055750, or 69618007059. The expiration dates range from March 27, 2025, to July 25, 2025.
Verify the NDC numbers and expiration dates listed in the recall notice to confirm if your product is affected.
The recall indicates a potential leakage risk after repackaging, but the product is not unsafe for normal use. Affected units should be checked for leakage.
Check for the NDC numbers 71399748005, 39328055750, or 69618007059 and expiration dates from March 27, 2025, to July 25, 2025.
The recall does not specify a remedy, so contact Safecor Health for further instructions.
We’ve drafted a message you can send Safecor to request your refund or repair — edit it as you like.
Subject: Recall D-0252-2025 — Safecor Safecor Hello, I own a Safecor that is covered by recall D-0252-2025 from Safecor. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
