Precision Dose Inc. recalls
Every recall we track for Precision Dose Inc. — 8 in all, from 2013–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Precision Dose Inc. peaked in 2021 (3); 7 since 2017.
All FDA recall records for Precision Dose Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 2 | 0 | 2 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 1 | 1 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 3 | 3 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 1 | 1 |
Precision Dose Inc. recalls before 2017
Recalls on record by year.
Most common reasons for Precision Dose Inc. recalls
What to do if you have a recalled Precision Dose Inc. product
- Match the NDC and lot number on your bottle or box to the recall.
- Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first.
- Report side effects to FDA MedWatch.
All Precision Dose Inc. recalls
7 shown- UnratedDrug
Precision Dose Inc. recalls Glycopyrrolate Oral Solution, 1 mg/5 mL, delivers 5 mL, Rx only, Pkg: Precision Dose, Inc, S. Beloil, IL 61080,
Precision Dose recalls Glycopyrrolate Oral Solution (1 mg/5 mL) due to failed impurities and degradation specifications. This prescription medication may pose risks if used as intended.
Precision DoseJul 14, 2026 - UnratedDrug
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)
Precision Dose recalls acetaminophen oral suspension due to contaminated raw ingredients. Affected lots include 503679, 503693, 503715. Stop using and contact for details.
Precision DoseNov 1, 2021 - UnratedDrug
Precision Dose Inc. recalls Chlorhexidine Gluconate Oral Rinse USP 0.12%, packaged in a) 15 mL x 30 Unit Dose Cups (30-pack case) NDC 68094-028-61,
Precision Dose Inc. recalls 0.12% Chlorhexidine Gluconate Oral Rinse due to cGMP deviations. Products sold in 30-pack and 100-pack cases with specific lot numbers from 2021-2022.
Precision DoseJan 1, 2021 - UnratedDrug
Precision Dose Inc. recalls Ranitidine Oral Solution, USP, 150 mg/10 mL, [10 mL x 30 Unit Dose Cups per case, NDC: 68094-204-62; 10 mL x 100 Unit
Precision Dose recalls ranitidine oral solution due to impurity N-nitrosodimethylamine (NDMA) found in the active pharmaceutical ingredient. This product is prescription-only and may pose health risks.
Precision DoseNov 13, 2019 - Lower riskDrug
Precision Dose Inc. recalls Carbamazepine Oral Suspension USP, 100 mg/5 mL, 5 mL Unit Dose Cups (NDC 68094-301-59), packaged in 10-count cups per
Precision Dose recalls 10-count carbamazepine oral suspension cups due to low drug potency. This may result in ineffective treatment. Check your product details and contact the manufacturer for guidance.
Precision DoseSep 25, 2017 - Lower riskDrug
Precision Dose Inc. recalls Carbamazepine Oral Suspension, USP. 100 mg/5 mL, 5 mL Unit Dose Cups, Rx Only, Pkg: Precision Dose, Inc., S. Beloit, IL
Precision Dose recalls Carbamazepine Oral Suspension due to labeling error in product carton. The carton lists incorrect volume and NDC number, but unit dose cups are correctly labeled.
Precision DoseJul 5, 2017 - Use cautionDrug
Precision Dose Inc. recalls Children's Acetaminophen Oral Suspension, 650 mg/20.3 mL unit dose cup (NDC 68094-650-59), packaged in 30-count cups
Precision Dose Inc. recalls Children's Acetaminophen Oral Suspension because the 650 mg dose is an adult strength, making the 'Children's' label misleading.
Precision DoseMar 21, 2013
Precision Dose Inc. recall questions
How many recalls has Precision Dose Inc. had?
8 recalls from Precision Dose Inc. are on record with U.S. safety agencies, from 2013–2026.
What is the most recent Precision Dose Inc. recall?
Precision Dose Inc. recalls Glycopyrrolate Oral Solution, 1 mg/5 mL, delivers 5 mL, Rx only, Pkg: Precision Dose, Inc, S. Beloil, IL 61080,, dated Jul 14, 2026. Every Precision Dose Inc. recall is listed on this page, newest first.
Why are Precision Dose Inc. products recalled?
The most common reasons on record: cGMP Deviations: Product manufactured with contaminated raw ingredient. (2).
What should I do if I have a recalled Precision Dose Inc. product?
Match the NDC and lot number on your bottle or box to the recall. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first. Report side effects to FDA MedWatch.
How do I get alerts for new Precision Dose Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.