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 Dose Glycopyrrolate Oral Solution Recall: Impurities Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/309294-precision-dose-glycopyrrolate-oral-solution-recall-impurities-risk. Based on FDA recall #D-0741-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0741-2026%22&limit=1).
The FDA announced on July 14, 2026, that Precision Dose Inc. is recalling Glycopyrrolate Oral Solution due to failed impurity specifications. The agency issued recall number D-0741-2026 for the voluntary Class II action.
How to tell if you have it
Brand: Precision Dose
Product: Glycopyrrolate Oral Solution, 1 mg/5 mL
NDCs: 68094-073-01 (oral syringe) and 68094-073-58 (case)
Lot #: 506033
Expiration Date: 11/30/2026
The hazard
The recall addresses failed impurities and degradation specifications in the product. The FDA classified this as a Class II recall.
Context
GovInfoNow's records show Precision Dose Inc. has had six other recalls since March 21, 2013. Other recent recalls of similar products include Novadoz Glycopyrrolate Oral Solution Recall (Dec. 15, 2025), SUN PHARMACEUTICAL Clindamycin Phosphate Topical Solution Recall (Nov. 26, 2025), and Somerset Therapeutics Dexamethasone Injection Recall (Feb. 4, 2026).
How to tell if you have this one
Check for the product name 'Glycopyrrolate Oral Solution', 1 mg/5 mL, with NDC codes 68094-073-01 (syringe) or 68094-073-58 (case). Look for lot number 506033 or expiration date 11/30/2026.
Brand
Precision Dose
Category
Drug
Based on the official FDA remedy
What to do — step by step
Check Product Details
Verify the NDC codes and expiration date to confirm if your product is affected.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 15 days after the firm started it.
1Firm started the recall
2Published in FDA’s Enforcement Report
3FDA classified it Class II
4Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
The recall states the product failed impurities and degradation specifications, so it may not be safe. Do not use this product without confirming it's not recalled.
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-0741-2026 (July 14, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0741-2026 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.