D-0725-2026 Class II Ongoing
FDA drug recall D-0725-2026 was initiated by Fresenius Kabi USA, LLC on July 16, 2026 and is designated Class II. Reason for recall: Presence of Particulate Matter: Hair was found in product The recall status is ongoing. Affected quantity: 59,425 vials.
Recall Details
- Product Type
- Drugs
- Report Date
- July 29, 2026
- Initiation Date
- July 16, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 59,425 vials
Product Description
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
Reason for Recall
Presence of Particulate Matter: Hair was found in product
Distribution Pattern
Nationwide within in the USA
Code Information
Lot #: 6134349, 6134620 Exp. Date 11/2026