Eugia US recalls
Eugia US has 17 recalls on record with the FDA and USDA, the earliest in 2023 and the latest reported on 10 Jun 2026. 16 are still ongoing. 1 was reported in the last 12 months. The most frequent reason is potency & assay.
Total recalls 17 since 2023
Last 12 months 1 reported
Class I 1 6% of total
Ongoing 16 latest 10 Jun 2026
Recalls per month, last 24 months click a bar for that month
Severity split
Class I 1 6% Class II 14 82% Class III 2 12%
Ongoing eugia us recalls 16 active
Reported Class Recall Company Reason Where 10 Jun 2026 Drug CLASS III Lidocaine HCl Injection, USP 2%, 40 mg recalled by Eugia US Lidolog Kit Eugia US Other Nationwide 25 Jun 2025 Drug CLASS II Gentamicin Injection, USP, (Pediatric), 20 mg recalled by Eugia US Gentamicin Eugia US Potency & Assay Nationwide 7 May 2025 Drug CLASS II Tirofiban Hydrochloride Injection 5 mg recalled by Eugia US Tirofiban Eugia US Potency & Assay Nationwide 7 May 2025 Drug CLASS II Tirofiban Hydrochloride Injection 12.5 mg recalled by Eugia US Tirofiban Eugia US Potency & Assay Nationwide 23 Apr 2025 Drug CLASS II Testosterone Cypionate Injection, USP, CIII, 200mg per mL recalled Testosterone Cypionate Eugia US Manufacturing (CGMP) Deviations Nationwide 15 Jan 2025 Drug CLASS II medroxyPROGESTERone Acetate Injectable Suspension, USP, 150mg per mL recalled Medroxyprogesterone Acetate Eugia US Manufacturing (CGMP) Deviations Nationwide
All eugia us recalls, newest first 17 total
Reported Class Recall Company Reason Where 10 Jun 2026 Drug CLASS III Lidocaine HCl Injection, USP 2%, 40 mg recalled by Eugia US Lidolog Kit Eugia US Other Nationwide 25 Jun 2025 Drug CLASS II Gentamicin Injection, USP, (Pediatric), 20 mg recalled by Eugia US Gentamicin Eugia US Potency & Assay Nationwide 7 May 2025 Drug CLASS II Tirofiban Hydrochloride Injection 5 mg recalled by Eugia US Tirofiban Eugia US Potency & Assay Nationwide 7 May 2025 Drug CLASS II Tirofiban Hydrochloride Injection 12.5 mg recalled by Eugia US Tirofiban Eugia US Potency & Assay Nationwide 23 Apr 2025 Drug CLASS II Testosterone Cypionate Injection, USP, CIII, 200mg per mL recalled Testosterone Cypionate Eugia US Manufacturing (CGMP) Deviations Nationwide 15 Jan 2025 Drug CLASS II medroxyPROGESTERone Acetate Injectable Suspension, USP, 150mg per mL recalled Medroxyprogesterone Acetate Eugia US Manufacturing (CGMP) Deviations Nationwide 15 Jan 2025 Drug CLASS II Progesterone Injection USP, 500mg per (50mg/mL) Multiple Dose Vial recalled Progesterone Eugia US Particulate Matter Nationwide 7 Aug 2024 Drug CLASS II Progesterone Injection, USP, 500 mg per (50mg/mL) Multiple-Dose Vial recalled Progesterone Eugia US Particulate Matter Nationwide 26 Jun 2024 Drug CLASS III Eptifibatide injection 20mg/ (2mg/mL) Single-Dose Vial recalled Eptifibatide Eugia US Potency & Assay Nationwide 26 Jun 2024 Drug CLASS II Dexamethasone Sodium Phosphate injection USP, 120mg recalled by Eugia US Dexamethasone Sodium Phosphate Eugia US Potency & Assay Nationwide 17 Apr 2024 Drug CLASS I Methocarbamol Injection, USP 1000mg recalled by Eugia US Methocarbamol Eugia US Particulate Matter Nationwide 27 Mar 2024 Drug CLASS II Nicardipine Hydrochloride Injection (2.5mg/mL), US, 25mg per Vial recalled Nicardipine Hydrochloride Eugia US Potency & Assay Nationwide 27 Mar 2024 Drug CLASS II Nicardipine Hydrochloride Injection, USP 25mg/mL (2.5 mg/mL) vials recalled Nicardipine Hydrochloride Eugia US Potency & Assay Nationwide 20 Mar 2024 Drug CLASS II Tobramycin for Injection, USP per Pharmacy recalled by Eugia US Tobramycin Eugia US Potency & Assay Nationwide 13 Mar 2024 Drug CLASS II Methylprednisolone acetate Injectable Suspension recalled by Eugia US Methylprednisolone Acetate Eugia US Potency & Assay 4 states 11 Oct 2023 Drug CLASS II Triamcinolone Acetonide Injectable Suspension recalled by Eugia US Triamcinolone Acetonide Eugia US Particulate Matter Nationwide 11 Jan 2023 Drug CLASS II Acyclovir Sodium Injection 1,000 mg per* (50 mg/mL) recalled by Eugia US Acyclovir Sodium Eugia US Particulate Matter Nationwide
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.