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Lower risk Drug recall · FDA · Published March 7, 2018

Apollo Care Vancomycin IV Bag: Stability Issue May Reduce Effectiveness

Apollo Care recalls Vancomycin 1.25g IV bags due to stability concerns beyond 90 days from use date. This affects certain lots manufactured in 2018. No immediate action needed but check expiration dates.

🇺🇸 FDA recall #D-0615-2018DrugApollo Care ›
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Recalling firmApollo Care3801 Mojave Ct Ste 101 · Columbia, MO 65202-4042
✎ GovInfoNow plain-language explainer

What happened, in plain English

Apollo Care is recalling specific Vancomycin 1.25g IV bags that may lose effectiveness after the use date. This is a stability issue that could reduce the medication's effectiveness if used beyond the recommended timeframe. Read more at govinfonow.com/recall/40785-apollo-care-vancomycin-iv-bag-stability-issue-may-reduce-effectiveness.

Source Summary by GovInfoNow · govinfonow.com/recall/40785-apollo-care-vancomycin-iv-bag-stability-issue-may-reduce-effectiveness · Updated October 7, 2026 · FDA enforcement record: FDA #D-0615-2018

Cite this page

“Apollo Care Vancomycin IV Bag: Stability Issue May Reduce Effectiveness.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/40785-apollo-care-vancomycin-iv-bag-stability-issue-may-reduce-effectiveness. Based on FDA recall #D-0615-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0615-2018%22&limit=1).

Why it’s dangerous

The stability data for these IV bags does not support using them beyond 90 days from the use date. This means the medication may become less effective over time, potentially requiring re-dosing or alternative treatments.

Who’s affected

Healthcare professionals using the recalled Vancomycin IV bags for patient treatment. Patients receiving this medication are at low risk since the issue relates to medication stability rather than immediate safety.

How to tell if you have this one

Check for the lot number AC-015569 on the IV bag. The product was manufactured with an expiration date of March 26, 2018. This specific lot was distributed by Apollo Care in Columbia, MO.

  • 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-0614-2018Vancomycin 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-015565, Exp. 03/26/2018144 bags
D-0615-2018Vancomycin 1.25g added to 250 mL of 0.9% Sodium Chloride IV bag, Rx only, APOLLOcare, 3801 Mojave Ct., Suite 101, Columbia, MO 65202, NDC 71170-254-25.; Lot#: AC-015569, Exp. 03/26/201896 bags
Based on the official FDA remedy

What to do — step by step

  1. Check Expiration Date

    Verify the expiration date on the IV bag to ensure it is within the 90-day timeframe from the use date.

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: Mar 7, 201812. FDA classified it Class II: Mar 29, 201823. Published in FDA’s Enforcement Report: Apr 4, 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.

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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-0615-2018 (March 7, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0615-2018 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