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Drug recall · FDA · Published February 14, 2024

Golden State Medical Supply Inc. recalls Fluticasone Propionate Nasal Spray USP, 50 mcg per spray, 120 metered sprays, 16 g net fill, Rx only, Manufactured by:

Golden State Medical Supply recalls Fluticasone Propionate Nasal Spray (50 mcg/spray) due to suspected Burkholderia cepacia complex contamination. This may pose health risks to users. Contact for return instructions.

🇺🇸 FDA recall #D-0349-2024DrugGolden State Medical Supply ›
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Contact the company & request your remedy

Recalling firmGolden State Medical Supply Inc.5187 Camino Ruiz · Camarillo, CA 93012-8601
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
✎ GovInfoNow plain-language explainer

What happened, in plain English

Golden State Medical Supply is recalling Fluticasone Propionate Nasal Spray (50 mcg per spray) because it may contain Burkholderia cepacia complex, a potential contaminant that could cause health issues. This recall affects prescription nasal sprays sold with specific lot numbers and expiration dates. Read more at govinfonow.com/recall/32818-golden-state-medical-supply-fluticasone-nasal-spray-recall-potential-burkholderia.

Source Summary by GovInfoNow · govinfonow.com/recall/32818-golden-state-medical-supply-fluticasone-nasal-spray-recall-potential-burkholderia · Updated September 23, 2026 · FDA enforcement record: FDA #D-0349-2024

Cite this page

“Golden State Medical Supply Fluticasone Nasal Spray Recall: Potential Burkholderia cepacia Contamination.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/32818-golden-state-medical-supply-fluticasone-nasal-spray-recall-potential-burkholderia. Based on FDA recall #D-0349-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0349-2024%22&limit=1).

Why it’s dangerous

Burkholderia cepacia complex is a type of bacteria that can cause serious infections, particularly in people with weakened immune systems. The suspected presence of this bacteria in the nasal spray could lead to health complications if the product is used.

Who’s affected

Prescription users of Fluticasone Propionate Nasal Spray (50 mcg per spray) with lot number TX5275 and expiration date 10/31/2026 are affected. Individuals with compromised immune systems may be at higher risk.

How to tell if you have this one

Check for the lot number TX5275 on the product label. The product was manufactured by Apotek Inc. in Toronto, Ontario, Canada and marketed by Golden State Medical Supply in Camarillo, California. The expiration date is 10/31/2026.

  • Brand
    Golden State Medical Supply
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the lot number TX5275 and expiration date 10/31/2026 on the nasal spray label.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The recall states there is a suspected potential presence of Burkholderia cepacia complex, which could pose health risks. The product may not be safe to use as it has been recalled.

How do I know if I have the recalled product?

Check for the lot number TX5275 and expiration date 10/31/2026 on the product label. The product was manufactured by Apotek Inc. in Toronto, Ontario, Canada and marketed by Golden State Medical Supply in Camarillo, California.

What should I do if I have the recalled product?

The recall does not specify a remedy, so contact Golden State Medical Supply for further instructions.

Take action

Contact Golden State Medical Supply

We’ve drafted a message you can send Golden State Medical Supply to request your refund or repair — edit it as you like.

Subject: Recall D-0349-2024 — Golden State Medical Supply Golden State Medical Supply

Hello,

I own a Golden State Medical Supply that is covered by recall D-0349-2024 from Golden State Medical Supply.

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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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-0349-2024 (February 14, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0349-2024 to see it in context.
  • Plain-language summary written by qwen3:4b on September 23, 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