Every recall we track for Eugia US LLC — 17 in all — plus the complaints and injury reports the public filed about them.
Eugia US LLC recalls Lidocaine HCl Injection 2% vials due to label wrap covering barcode, making scanning difficult. Affected units have specific NDC and lot numbers.
Eugia US LLC recalls pediatric gentamicin injections with failed stability tests. These vials may not be safe for use after expiration. Check your vial's batch number and expiration date.
Eugia US LLC recalls Tirofiban Hydrochloride Injection 5 mg/100 mL due to out-of-spec related substances test results from stability studies. This medication is prescription-only and sold in single-dose containers.
Eugia US LLC recalls Tirofiban Hydrochloride Injection 12.5 mg/250 mL due to out-of-spec related substances in stability testing. This medication is prescription-only and sold in single-dose containers.
Eugia recalls 200mg testosterone vials due to crystals not redissolving after warming. This affects patients using the injection for medical treatment. Contact Eugia for details.
Eugia recalls progesterone injections with glass particles found in vials. This may cause injury during medical use. Affected vials were manufactured in India with specific batch numbers.
Eugia US LLC recalls 150mg per mL medroxyprogesterone acetate injectable vials manufactured in India due to CGMP deviations. This is a prescription-only product for medical use.
Eugia US LLC recalls 500 mg progesterone injections due to glass particles in vials. Affected lots from India manufacturing; stop using if you have this product.
Eugia US LLC recalls Dexamethasone Sodium Phosphate injection vials with impurity sulfonic acid adducts above specifications. Affected vials have specific lot numbers and expiration dates. Contact for remedy details.
Eugia US LLC recalls Eptifibatide injection vials made in India with failed impurities that could pose health risks. Affected units have specific NDC and lot numbers.
Eugia US LLC recalls Tobramycin for Injection, USP, 1.2 grams per Pharmacy Bulk Package for potential stability issues. This product was manufactured in India and distributed to US pharmacies. Check your carton NDC 55150-470-06 and vial NDC 55150-470-01 for affected lots.
Eugia US LLC recalls 400mg per 5mL Methylprednisolone acetate Injectable Suspension due to failed dissolution specifications. This medication is for prescription use only and was manufactured in India. Consumers should contact the manufacturer for details.
Eugia US LLC recalls Nicardipine Hydrochloride Injection (25mg/10mL) due to failed impurities tests. This medication is prescription-only and may pose health risks if used improperly.
Eugia US LLC recalls 10mL Methocarbamol injection vials due to particulate matter. This may cause serious injury if injected. Affected units were manufactured in India with specific lot number.
Eugia US LLC recalls Acyclovir Sodium Injection vials due to customer reports of dark particles. This may cause injury if injected. Check your vial's lot number and contact the manufacturer for details.
