RecallRadar

FDA Drug recall D-0726-2026

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, La…

On 2026-07-29 the FDA classified a Class II recall of 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, La… by Fresenius Kabi Usa, citing presence of Particulate Matter: Hair was found in products.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0726-2026
ClassificationClass II
Statusongoing
Initiated2026-07-16
Published2026-07-29
Last updated2026-09-13 11:52 UTC
CompanyFresenius Kabi Usa
DistributionUS

Product

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

Presence of Particulate Matter: Hair was found in products

Identifiers

ndc63323-208-01
ndc63323-208-05
code_infoLot #: 6133801, Exp. Date 01/2028

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0726-2026%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.