FDA · Drugs ·
Glycopyrrolate Injection recall
Fresenius Kabi USA, LLC recalled Glycopyrrolate Injection on July 29, 2026 because of presence of Particulate Matter: Hair was found in product. It was sold nationwide.
Why it was recalled
Presence of Particulate Matter: Hair was found in product
What's recalled
Glycopyrrolate Injection, USP, 1 mg per 5 mL (0.2 mg per mL), 25 x 5 mL fill in a 6.5 mL vial, Rx only, Multiple Dose Vials, Fresenius Kabi, Lake Zurich, IL 60047 NDC Tray: 63323-578-05; NDC Vial: 63323-578-07
Quantity: 59,425 vials
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- Fresenius Kabi USA, LLC, Lake Zurich, IL
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
Nationwide within in the USA - Status
- Ongoing
- Recall number
- D-0725-2026
- Source
- U.S. Food and Drug Administration
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