Spectrum Laboratory Products recalls Fentanyl Citrate USP, Active Pharmaceutical Ingredient, Spectrum Chemical MFG. CORP., Gardena, CA 90248 NDC
Spectrum Laboratory Products recalls Fentanyl Citrate USP active pharmaceutical ingredient due to potential glass contamination from supplier. This may pose a risk of injury if ingested. Check your NDC 49452-0032-06, lots 1HE0899 or 1IB0005.
Recall notice
CGMP Deviations: Received notice from supplier that there is potential glass contamination.
Contact the company & request your remedy
What happened, in plain English
Spectrum Laboratory Products is recalling Fentanyl Citrate USP active pharmaceutical ingredients because they may contain glass particles from a supplier. This could cause injury if the product is used improperly. Read more at govinfonow.com/recall/37999-spectrum-fentanyl-citrate-usp-recall-potential-glass-contamination-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/37999-spectrum-fentanyl-citrate-usp-recall-potential-glass-contamination-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-0141-2020
Cite this page
“Spectrum Fentanyl Citrate USP Recall: Potential Glass Contamination Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37999-spectrum-fentanyl-citrate-usp-recall-potential-glass-contamination-risk. Based on FDA recall #D-0141-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0141-2020%22&limit=1).
Why it’s dangerous
Glass contamination in the product could cause injury if the substance is ingested or injected. The supplier's notice indicates potential glass particles in the active pharmaceutical ingredient.
Who’s affected
People who have the specific Fentanyl Citrate USP active pharmaceutical ingredient with NDC 49452-0032-06, lots 1HE0899 or 1IB0005 are affected. Healthcare professionals using this product for medical purposes are at highest risk.
How to tell if you have this one
Check for NDC 49452-0032-06 with lots 1HE0899 or 1IB0005. The product was manufactured in Gardena, CA and expired February 28, 2023.
- Brand
Spectrum Laboratory Products- Category
Drug
What to do — step by step
Check Product Details
Identify if your Fentanyl Citrate USP active pharmaceutical ingredient has NDC 49452-0032-06 and lots 1HE0899 or 1IB0005.
Questions people ask
Is this product safe to use?
The recall states there is potential glass contamination, which could cause injury if used. The official notice does not specify if the product is safe to use.
What should I do if I have this product?
The recall does not provide a remedy or action steps for affected products.
How can I check if my product is recalled?
Check for NDC 49452-0032-06 with lots 1HE0899 or 1IB0005. The product was manufactured in Gardena, CA and expired February 28, 2023.
Contact Spectrum Laboratory Products
We’ve drafted a message you can send Spectrum Laboratory Products to request your refund or repair — edit it as you like.
Subject: Recall D-0141-2020 — Spectrum Laboratory Products Spectrum Laboratory Products Hello, I own a Spectrum Laboratory Products that is covered by recall D-0141-2020 from Spectrum Laboratory Products. 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-0141-2020 (September 12, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0141-2020 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 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.