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Unrated Drug recall · FDA · Published July 25, 2016

US Compounding Inc recalls Docusate Oral 10 mg/mL syringes due to microbial contamination

US Compounding Inc recalls Docusate Oral 10 mg/mL syringes (1mL, 2mL, 5mL) because of microbial contamination with B. cepacia. Affected products were sold nationwide with all lots.

🇺🇸 FDA recall #D-0219-2017DrugUS Compounding Inc ›
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Recalling firmUS Compounding Inc1270 Don's Lane · Conway, AR 72032
✎ GovInfoNow plain-language explainer

What happened, in plain English

US Compounding Inc is recalling Docusate Oral 10 mg/mL syringes (1mL, 2mL, and 5mL) due to microbial contamination with B. cepacia. This contamination could cause serious health risks if the product is used. Read more at govinfonow.com/recall/42538-us-compounding-inc-recalls-docusate-oral-10-mg-ml-syringes.

Source Summary by GovInfoNow · govinfonow.com/recall/42538-us-compounding-inc-recalls-docusate-oral-10-mg-ml-syringes · Updated October 9, 2026 · FDA enforcement record: FDA #D-0219-2017

Cite this page

“US Compounding Inc recalls Docusate Oral 10 mg/mL syringes due to microbial contamination.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/42538-us-compounding-inc-recalls-docusate-oral-10-mg-ml-syringes. Based on FDA recall #D-0219-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0219-2017%22&limit=1).

Why it’s dangerous

The syringes were contaminated with B. cepacia, a type of bacteria that can cause infections. Using contaminated medication may lead to serious health issues, especially for individuals with weakened immune systems.

Who’s affected

People who have purchased or use Docusate Oral 10 mg/mL syringes from US Compounding Inc. Those with medical conditions requiring frequent use of this medication are at higher risk.

How to tell if you have this one

Check for syringes labeled as Docusate Oral 10 mg/mL with lot numbers 62295-0601-01 (1mL), 62295-0601-02 (2mL), or 62295-0601-05 (5mL). These products were sold nationwide with all lots.

  • Brand
    US Compounding Inc
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for syringes labeled Docusate Oral 10 mg/mL with lot numbers 62295-0601-01, 62295-0601-02, or 62295-0601-05.

Where it went and when

Where it was distributed

Distributed in Texas.

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: not listedMOKentucky: 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: yesTXFlorida: not listedFL

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

States: Texas.

Recall timeline

FDA terminated this recall 8 months after the firm started it.

1. Firm started the recall: Jul 25, 201612. FDA classified it Class I: Dec 22, 201623. Published in FDA’s Enforcement Report: Dec 28, 201634. FDA terminated the recall: Apr 6, 2017420162017
  1. Firm started the recall
  2. FDA classified it Class I
  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-0219-2017 (July 25, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0219-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 9, 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