Reported Nov 17, 2021 · Terminated

Acetaminophen Oral Suspension, 325 mg/10.15 mL, packaged in 10.15 mL per cup (NDC Individual cup

Precision Dose Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Precision Dose Inc. · 722 Progressive Ln · South Beloit, IL · 61080-2616

Is this the product you have?

Acetaminophen Oral Suspension, 325 mg/10.15 mL, packaged in 10.15 mL per cup (NDC Individual cup

3 of 3 products

Products covered by this recall
#Product as published
130-count case (NDC 30-count case: 68094-330-62), and
2100-count case (NDC 100-count case: 68094-330-61), Hospital Use Only, Pkg. Precision Dose, Inc.
3Beloit, IL 61080.
Lot codes and dates
    • Lot#: 503679
    • 503693
    • 503715
Amount recalled
151,100 unit dose cups

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide

Why it was recalled

cGMP Deviations: Product manufactured with contaminated raw ingredient.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Jul 14, 2024 · Data as of Sep 19, 8:02 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.