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Unrated Drug recall · FDA · Published August 22, 2017

Centurion Labs Ninjacof-A Oral Solution Recall: Microbial Contamination Risk

Centurion Labs recalls Ninjacof-A oral solution due to potential B. cepacia contamination. Consumers should check product details and contact the company for guidance.

🇺🇸 FDA recall #D-1141-2017DrugCenturion Labs ›
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Contact the company

Recalling firmCenturion Labs, LLC3100 Bowling Dr, Suite 1 · Birmingham, AL 35242-6588
✎ GovInfoNow plain-language explainer

What happened, in plain English

Centurion Labs is recalling Ninjacof-A oral solution because it may contain harmful bacteria. This could cause illness if taken, so affected users should stop using it and contact the company. Read more at govinfonow.com/recall/41330-centurion-labs-ninjacof-a-oral-solution-recall-microbial-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/41330-centurion-labs-ninjacof-a-oral-solution-recall-microbial-contamination-risk · Updated October 7, 2026 · FDA enforcement record: FDA #D-1141-2017

Cite this page

“Centurion Labs Ninjacof-A Oral Solution Recall: Microbial Contamination Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/41330-centurion-labs-ninjacof-a-oral-solution-recall-microbial-contamination-risk. Based on FDA recall #D-1141-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1141-2017%22&limit=1).

Why it’s dangerous

The product may be contaminated with B. cepacia bacteria, which can cause infections. This contamination could lead to illness if the solution is consumed, especially in vulnerable individuals.

Who’s affected

People who own or use Ninjacof-A oral solution with the specific lot number and expiration date listed in the recall. Children and those with weakened immune systems may be at higher risk.

How to tell if you have this one

Check for the product name 'Ninjacof-A (Acetaminophen 160 mg, Chlophedianol HCL 12.5 mg and Pyrilamine Maleate 12.5 mg) Oral Solution, 16 fl. oz.' with the lot number 201NA1601 and expiration date 11/2018.

  • Brand
    Centurion Labs
  • 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
    Nationwide.
Recall numberProduct, codes & lotsQuantityNDC
D-1140-2017Ninjacof (Chlophedianol HCL 12.5 mg and Pyrilamine Maleate 12.5 mg) Oral Solution, 16 fl. oz. (473 mL), Cotton Candy Flavor, Manufactured for: Centurion Labs, LLC Birmingham, AL 35243 --- NDC 23359-032-16; Lot: 200N1601 Exp. 11/20184149 bottles23359-032-16, 23359-032-10, 23359-032-04
D-1141-2017Ninjacof-A (Acetaminophen 160 mg, Chlophedianol HCL 12.5 mg and Pyrilamine Maleate 12.5 mg) Oral Solution, 16 fl. oz. (473 mL), Cotton Candy Flavor, Manufactured for: Centurion Labs, LLC Birmingham, AL 35243 --- NDC 23359-033-16; Lot: 201NA1601 Exp. 11/2018621 bottles—
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the lot number 201NA1601 and expiration date 11/2018 on the product label.

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

Distributed nationwide.

Recall timeline

FDA terminated this recall 3.1 years after the firm started it.

1. Firm started the recall: Aug 22, 201712. FDA classified it Class II: Sep 12, 201723. Published in FDA’s Enforcement Report: Sep 20, 201734. FDA terminated the recall: Sep 14, 2020420172020
  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-1141-2017 (August 22, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1141-2017 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