The Recall Desk
Agency classClass IIOur severity:ModerateFDA (Drugs)·D-1522-2016·Announced 2016-10-05

Pharmatech Recalls Ninjacof-A Liquid Due to Potential B. cepacia Contamination

Pharmatech LLC is recalling Ninjacof-A liquid due to a potential risk of contamination with B. cepacia bacteria. This is a precautionary measure.

The agency’s classification

FDA (Drugs): Class II

Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 2/5 (Moderate).

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II and is described as a precautionary measure due to a potential risk of contamination, with no reported illnesses or injuries.

Plain-English summary

Pharmatech LLC is recalling 1,332 bottles of Ninjacof-A (acetaminophen, chlophedianol HCl, pyrilamine maleate) Liquid. The product is a 16 fl oz (473 mL) bottle with NDC 23359-033-16, manufactured for Centurion Labs, LLC. The specific lot number is 25321601, with an expiration date of 04/18.

The recall was initiated as a precautionary measure due to a potential risk of product contamination with the bacteria B. cepacia. The agency classified this as a Class II recall. The product was distributed nationwide.

Consumers should stop using the recalled product and contact Pharmatech LLC or their healthcare provider for further instructions.

The recalled product

Product
Ninjacof-A (acetaminophen, chlophedianol HCl, pyrilamine maleate) Liquid, 160 mg/12.5 mg/12.5 mg in each 5 mL, 16 fl oz (473 mL) bottle, Manufactured for: Centurion Labs, LLC, Birmingham, AL 35243, NDC 23359-033-16.
Manufacturer
Pharmatech LLC
Affected units
1,332

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (2)

  • Lot #: 25321601
  • Exp 04/18

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 7 recalled by Pharmatech LLC under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 7 products in this recall →

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