Skip to content
Lower risk Drug recall · FDA · Published February 15, 2018

Apollo Care Vancomycin IV Bags: Stability Issue May Reduce Effectiveness

Apollo Care recalls Vancomycin 1g IV bags due to stability concerns beyond 90 days from use date. This affects prescription-only products sold in Columbia, MO. Contact for details.

🇺🇸 FDA recall #D-0579-2018DrugApollo Care ›
Take action

Contact the company

Recalling firmApollo Care3801 Mojave Ct Ste 101 · Columbia, MO 65202-4042
✎ GovInfoNow plain-language explainer

What happened, in plain English

Apollo Care is recalling Vancomycin 1g IV bags mixed with 0.9% Sodium Chloride. The recall happens because the product's stability doesn't support using it beyond 90 days past the expiration date, which could lead to reduced effectiveness. Read more at govinfonow.com/recall/40809-apollo-care-vancomycin-iv-bags-stability-issue-may-reduce-effectiveness.

Source Summary by GovInfoNow · govinfonow.com/recall/40809-apollo-care-vancomycin-iv-bags-stability-issue-may-reduce-effectiveness · Updated October 7, 2026 · FDA enforcement record: FDA #D-0579-2018

Cite this page

“Apollo Care Vancomycin IV Bags: Stability Issue May Reduce Effectiveness.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/40809-apollo-care-vancomycin-iv-bags-stability-issue-may-reduce-effectiveness. Based on FDA recall #D-0579-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0579-2018%22&limit=1).

Why it’s dangerous

The product's stability data doesn't support keeping it beyond 90 days after the use date. This means the medication might not work as intended after that period, potentially reducing its effectiveness.

Who’s affected

Healthcare professionals who use prescription Vancomycin IV bags from Apollo Care. Patients receiving this medication are at low risk since it's a controlled medical product.

How to tell if you have this one

Check for the Apollo Care brand, 1g Vancomycin in 250mL of 0.9% Sodium Chloride IV bags with NDC 71170-254-25. The lot number AC-015558 was produced for expiration 03/07/2018.

  • Brand
    Apollo Care
  • Category
    Drug
FDA recall event · 2 products

All 2 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
    Terminated
  • Distribution
    Medical Facility in MO
Recall numberProduct, codes & lotsQuantity
D-0579-2018Vancomycin 1g added to 250mL of 0.9% Sodium Chloride IV bag, Rx only, APOLLOcare, 3801 Mojave Ct., Suite 101, Columbia, MO 65202, NDC 71170-254-25.; Lot: AC-015558, Exp 03/07/2018360 bags
D-0580-2018Vancomycin 1.25g added to 250mL of 0.9% Sodium Chloride IV bag, Rx only, APOLLOcare, 3801 Mojave Ct., Suite 101, Columbia, MO 65202, NDC 71170-264-25.; Lot: AC-015560, Exp 03/14/2018312 bags
Based on the official FDA remedy

What to do — step by step

  1. Check Expiration Date

    Verify the product's expiration date is within 90 days of the use date to ensure stability.

Where it went and when

Where it was distributed

Distributed in Missouri.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: yesMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

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

States: Missouri.

Recall timeline

FDA terminated this recall 3 months after the firm started it.

1. Firm started the recall: Feb 15, 201812. FDA classified it Class II: Mar 6, 201823. Published in FDA’s Enforcement Report: Mar 14, 201834. FDA terminated the recall: May 31, 201842018
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

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

Similar recalls

Latest drug recalls

Keep exploring

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-0579-2018 (February 15, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0579-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 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