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Lower risk Drug recall · FDA · Published June 19, 2017

Fagron Sterile Services Recalls Succinylcholine Chloride Syringes Due to Sterility Risk

Fagron Sterile Services recalls specific Succinylcholine Chloride syringes (IV use only) due to lack of sterility assurance. This voluntary recall was initiated by the manufacturer to prevent potential infections.

🇺🇸 FDA recall #D-0946-2017DrugFagron Sterile Services ›
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Recalling firmFagron Compounding Services LLC dba Fagron Sterile Services8710 E 34th St N · Wichita, KS 67226-2636
✎ GovInfoNow plain-language explainer

What happened, in plain English

Fagron Sterile Services has recalled certain Succinylcholine Chloride syringes (100 mg per 5mL, 20 mg per mL) because they may not be sterile. This could lead to infections if used in medical procedures. The recall is voluntary and initiated by the manufacturer. Read more at govinfonow.com/recall/41552-fagron-sterile-services-recalls-succinylcholine-chloride-syringes-due-to-sterility.

Source Summary by GovInfoNow · govinfonow.com/recall/41552-fagron-sterile-services-recalls-succinylcholine-chloride-syringes-due-to-sterility · Updated October 8, 2026 · FDA enforcement record: FDA #D-0946-2017

Cite this page

“Fagron Sterile Services Recalls Succinylcholine Chloride Syringes Due to Sterility Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/41552-fagron-sterile-services-recalls-succinylcholine-chloride-syringes-due-to-sterility. Based on FDA recall #D-0946-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0946-2017%22&limit=1).

Why it’s dangerous

The syringes may not be sterile, which could lead to infections if used in medical procedures. This lack of sterility assurance is why the manufacturer initiated a voluntary recall.

Who’s affected

Healthcare professionals and patients receiving IV treatments with the recalled syringes. Those most at risk are individuals undergoing medical procedures requiring this medication.

How to tell if you have this one

Check for the UPC 7335968405, lot numbers C274-000000331, C274-000001274, or C274-000001326, and expiration dates up to August 30, 2017, September 7, 2017, or September 14, 2017.

  • Brand
    Fagron Sterile Services
  • Product
    Succinylcholine Chloride, 100 mg per 5mL, 20 mg per mL syringe. IV Use Only. JCB Laboratories, 8710 E 34th St., N
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the UPC 7335968405 or lot numbers C274-000000331, C274-000001274, or C274-000001326 on the syringe packaging.

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 terminated this recall 12 months after the firm started it.

1. Firm started the recall: Jun 19, 201712. FDA classified it Class II: Jul 6, 201723. Published in FDA’s Enforcement Report: Jul 12, 201734. FDA terminated the recall: Jun 12, 2018420172018
  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-0946-2017 (June 19, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0946-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 8, 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