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Ninjacof Recalled for B. Cepacia Infection Risk

Ninjacof Recalled for B. Cepacia Infection Risk

August 31, 2017 — Centurion Labs recalled Ninjacof and Ninjacof A Cold Medicine due to a risk of life-threatening bacterial infections.

Centurion Labs issued the recall after being notified by the FDA that Ninjacof was made in a facility that is contaminated with an antibiotic-resistant bacteria called Burkholderia cepacia (“B. cepacia”).

The FDA did not report any infections, but warned that B. cepacia infections can be severe or life-threatening in at-risk patients:

“Use of a product that may contain B. cepacia, could result in infections in patients with compromised immune systems and in patients with chronic lung conditions such as cystic fibrosis.”

The recall involves 2 lots of Ninjacof (473 mL bottles) with Expiration Dates of 11/2018, including:

  • Ninjacof Lot# 200N1601 (NDC 23359-032-16)
  • Ninjacof A with Lot# 201NA1601 (NDC 23359-033-16)

The recalled Ninjacof products were distributed in Alabama, Arkansas, Florida, Georgia, Louisiana, Missouri, Mississippi, New Jersey, North Carolina, Ohio, Oklahoma, South Carolina, Tennessee, and Texas.

Do I have a Ninjacof Lawsuit?

The Schmidt Firm, PLLC is currently accepting Ninjacof induced injury cases in all 50 states. If you or somebody you know has been infected with B. cepacia, you should contact our lawyers immediately for a free case consultation. Please use the form below to contact our Product Liability Litigation Group or call toll free 24 hours a day at (866) 920-0753.

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