Ninjacof Recalled for B. Cepacia Infection RiskAugust 31, 2017 — Centurion Labs has recalled certain bottles of Ninjacof and Ninjacof A cold medicine due to possible contamination with the bacteria B. cepacia.

The recall was issued after the FDA notified Centurion Labs that Ninjacof products were manufactured in a facility that is contaminated with Burkholderia cepacia.

No infections have been reported, but the FDA warns that B. cepacia infections may be 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 recalled products were sold in 473 mL bottles with the expiration date 11/2018, and include:

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

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

Ninjacof and Ninjacof A are medications that are used to treat the symptoms of the common cold, allergies, and other respiratory problems. Patients who use these products can potentially develop a deadly antibiotic-resistant infection with B. cepacia.

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