D-0725-2026 Class II Ongoing

Recalled by Fresenius Kabi USA, LLC — Lake Zurich, IL

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