D-0726-2026 Class II Ongoing

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

FDA drug recall D-0726-2026 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 products The recall status is ongoing. Affected quantity: 181,225 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
181,225 vials

Product Description

Lidocaine HCl Injection, USP, 2%, 100 mg per 5 mL (20 mg per mL), 25 Single Dose Vials, 5 mL per vial, Rx only, Sterile, Fresenius Kabi, Lake Zurich, IL 60047 NDC Tray: 63323-208-05; NDC Vial: 63323-208-01

Reason for Recall

Presence of Particulate Matter: Hair was found in products

Distribution Pattern

Nationwide within in the USA

Code Information

Lot #: 6133801, Exp. Date 01/2028