Precision Dose Acetaminophen Suspension Recall: Contaminated Raw Ingredient Risk

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Contact the company & request your remedy

Recalling firmPrecision Dose Inc.722 Progressive Ln, N/A · South Beloit, IL 61080-2616

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Precision Dose is recalling acetaminophen oral suspension products that were made with contaminated raw ingredients. This could pose a health risk if the product is used as intended.

Why it’s dangerous

The product was manufactured with contaminated raw ingredients, which could lead to health issues if consumed. The contamination occurred during the production process, potentially introducing harmful substances into the product.

Who’s affected

People who own or use the recalled acetaminophen oral suspension products. Hospital staff using the product are most at risk due to the hospital-only labeling.

How to tell if you have this one

Check for the product name 'Acetaminophen Oral Suspension, 325 mg/10.15 mL' with NDC numbers 68094-330-59 (individual cup), 68094-330-62 (30-count case), or 68094-330-61 (100-count case). The affected lots are 503679, 503693, and 503715.

Brand
Precision Dose
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Product Details
Look for the NDC numbers 68094-330-59, 68094-330-62, or 68094-330-61 on the packaging.
Contact Manufacturer
Reach out to Precision Dose Inc. for further instructions on handling the recalled product.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The recall states the product was manufactured with contaminated raw ingredients, so it is not safe to use as intended.

What lots are affected?

The affected lots are 503679, 503693, and 503715.

How do I know if I have the recalled product?

Check for the NDC numbers 68094-330-59 (individual cup), 68094-330-62 (30-count case), or 68094-330-61 (100-count case) on the packaging.

Take action

Contact Precision Dose

We’ve drafted a message you can send Precision Dose to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall D-0095-2022 — Precision Dose Precision Dose

Hello,

I own a Precision Dose that is covered by recall D-0095-2022 from Precision Dose.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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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-0095-2022 (November 1, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0095-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 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.

Precision Dose Inc. recalls Acetaminophen Oral Suspension, 325 mg/10.15 mL, packaged in 10.15 mL per cup (NDC Individual cup: 68094-330-59), in a)

Recall notice