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Asclemed USA, Inc. Recalls

2 recalls found for Asclemed USA, Inc.. Check current safety alerts and related brands before using affected products.

Active recalls: 2
Pages: 1

HIGH

FDA DRUG

Lidocaine HCl Injection, USP 2%, 40 mg/2 mL (20 mg/mL), 2 mL per Single-Dose Vial, Rx Only, Mfd. in India for: Eugia US LLC, E. Windsor, NJ 08520. NDC: 55150-164-02

Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan

May 18, 2026

LIDOLOG KIT

Labeling: Not

HIGH

FDA DRUG

Duloxetine DR Capsules, 30 mg, 30 count bottles, Rx, Relabeled by: Enovachem Pharmaceuticals, Torrance, CA 90501, NDC 76420-634-30, Marketed by: Ajanta Pharma USA Inc.

CGMP Deviations; presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-nitroso-duloxetine, above the FDA acceptable intake limit.

May 14, 2026

DULOXETINE

CGMP Deviations;

Brand Statistics

Total Recalls

2

Pages

1

Related Brands

LIDOLOG KIT DULOXETINE