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Lower risk Drug recall · FDA · Published February 17, 2025

Safecor Health Vitamin D Syringe Recall: Leakage Risk After Repackaging

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.

🇺🇸 FDA recall #D-0250-2025DrugSafecor Health ›
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Recalling firmSafecor Health, LLC4060 Business Park Dr Ste B · Columbus, OH 43204-5047
✎ GovInfoNow plain-language explainer

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. Read more at govinfonow.com/recall/32272-safecor-health-vitamin-d-syringe-recall-leakage-risk-after-repackaging.

Source Summary by GovInfoNow · govinfonow.com/recall/32272-safecor-health-vitamin-d-syringe-recall-leakage-risk-after-repackaging · Updated August 18, 2026 · FDA enforcement record: FDA #D-0250-2025

Cite this page

“Safecor Health Vitamin D Syringe Recall: Leakage Risk After Repackaging.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/32272-safecor-health-vitamin-d-syringe-recall-leakage-risk-after-repackaging. Based on FDA recall #D-0250-2025 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0250-2025%22&limit=1).

The FDA announced on Feb. 17, 2025, that Safecor Health, LLC is recalling Ergocalciferol Vitamin D Supplement oral syringes due to a defective delivery system causing leakage. The agency issued recall number D-0250-2025 for the voluntary Class II action.

How to tell if you have it

  • Brand: Safecor Health
  • Product: Ergocalciferol - Vitamin D Supplement - 10 mcg (400 Units) per 0.05 mL Oral Syringe, Delivers: 0.05 mL Oral Solution
  • Manufacturer: Westminster
  • Packer: Safecor Health, LLC, Columbus, OH 43204
  • NDC: 69367028302
  • Lot #: 24300812, Exp 01/31/2025; 24530836, Exp 07/19/2025
  • Quantity: 3069 Oral Syringes
  • Distribution: Nationwide in the USA

The hazard

The recall cites a defective delivery system where leakage was observed after the oral solution was repackaged into unit-dose syringes, according to the FDA.

Context

GovInfoNow's records show Safecor Health, LLC has 11 other recalls on record since 2015-03-02. Other recent recalls of similar products include Novocol OraVerse Injection Recall (2025-10-31), Somerset Therapeutics Dexamethasone Injection Recall (2026-02-04), and BD PurPrep Sterile Solution Recall (2026-04-22).

How to tell if you have this one

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.

  • Brand
    Safecor Health
  • Category
    Drug
FDA recall event · 5 products

All 5 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Ongoing
  • Distribution
    Nationwide in the USA
Recall numberProduct, codes & lotsQuantity
D-0250-2025Ergocalciferol - Vitamin D Supplement - 10 mcg (400 Units) per 0.05 mL Oral Syringe, Delivers: 0.05 mL Oral Solution, Mfg by: Westminster, Pkg by: Safecor Health, LLC, Columbus, OH 43204, NDC: 69367028302.; Lot #: 24300812, Exp 01/31/2025; 24530836, Exp 07/19/20253069 Oral Syringes
D-0251-2025Simethicone 20 mg per 0.3 mL Oral Syringe, Delivers: 0.3 mL, Oral Drops, Mfg By: Rugby, Pkg by: Safecor Health, LLC, Columbus, OH 43204, NDC: 00536130375.; Lot #s: 24201295, Exp 02/05/2025; 24210364, Exp 02/20/2025; 24231720, Exp 02/27/2025; 24500770, Exp 06/26/2025; 24471182, Exp 06/20/2025; 25031031, Exp 07/22/2025.10992 Oral Syringes
D-0252-2025Ferrous Sulfate 7.5 mg Iron/0.5 mL Oral Syringe, Delivers: 0.5 mL, Iron Supplement Drops, Mfg by: Akron Pharma, Pkg by: Safecor, Columbus, OH 43204. NDC: a) 71399748005, b) 39328055750, c) 69618007059.; Lot #s: a) 24250093, Exp 03/07/2025; 24321592, Exp 04/04/2025; 24280320, Exp 03/27/2025; b) 24371268, Exp 04/19/2025; c) 24400519, Exp 04/07/2025; 24500768, Exp 06/24/2025; 25040972, Exp 07/25/2025.1535 Oral Syringes
D-0253-2025Lorazepam 0.5 mg per 0.25 mL Oral Syringe, Delivers: 0.25 mL, Oral Concentrate, Rx Only, Refrigerate, Mfg by: PAI, Pkg by: Safecor Health, LLC, Columbus, OH 43204, NDC: a) 00054353244, b) 00121077001, c) 65162068784.; Lot #s: a) 24210274, Exp 01/31/2025; 24401700, Exp 04/25/2025; b) 24251067, Exp 03/25/2025; 24421733, Exp 06/03/2025; c) 24261384, Exp 03/24/2025; 24370127, Exp 04/28/2025.3465 Oral Syringes
D-0254-2025Morphine Sulfate 5 mg per 0.25 mL Oral Syringe, Delivers: 0.25 mL, Oral Solution, Rx Only, Mfg by: Hikma, Pkg by: Safecor Health, LLC, Columbus, OH 43204, NDC: a) 00406800312, b) 00406800330, c) 00054051750.; Lot #s: a) 24220672, Exp 02/19/2025; 24280145, Exp 03/18/2025; 24240711, Exp 03/19/2025; b) 24180729, Exp 01/23/2025; 25030427, Exp 07/17/2025; c) 24360865, 24360864, Exp 03/31/2025; 24480235, Exp 06/21/2025.12390 Oral Syringes
Based on the official FDA remedy

What to do — step by step

  1. Stop Using It Now

    Discard the syringe if you have the affected lot numbers to prevent potential contamination.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide in the USA” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 23 days after the firm started it.

1. Firm started the recall: Feb 17, 202512. FDA classified it Class II: Mar 5, 202523. Published in FDA’s Enforcement Report: Mar 12, 202532025
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

What happens if the syringe leaks?

The recall states that leakage may occur after repackaging, which could lead to contamination of surfaces or materials. However, no injuries have been reported.

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Where this comes from

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.

  • Official source: FDA Recall #D-0250-2025 (February 17, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0250-2025 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA