Asclemed USA recalls

Asclemed USA has 10 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 29 Jul 2026. 5 are still ongoing. 4 were reported in the last 12 months. The most frequent reason is potency & assay.

Total recalls10since 2018
Last 12 months4reported
Class I220% of total
Ongoing5latest 29 Jul 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 2 20%Class II 6 60%Class III 2 20%

By year

Ongoing asclemed usa recalls

5 active
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIILidolog Kit, Kit Contains: Lidocaine HCl Injection recalledLidolog KitAsclemed USAOtherTN
DrugCLASS IILidocaine HCl Injection USP, 1% (10 mg/mL) single dose ampule recalledLidocaine HydrochlorideAsclemed USASterilityNationwide
DrugCLASS IIAccucaine, Kit contains: Lidocaine HCl Injection recalledAccucaineAsclemed USASterilityNationwide
DrugCLASS IIDuloxetine DR Capsules, 30 mg, Rx, Relabeled recalled by Asclemed USADuloxetineAsclemed USANitrosamine ImpurityNationwide
DrugCLASS IIIAsclemed USA products recalledAsclemed USAOtherAL, CA, LA

All asclemed usa recalls, newest first

10 total

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.