LIDOLOG KIT Lidocaine HCl Injection, USP 2%, 40 mg/2 mL (20 mg/mL), 2 mL per Single-Dose recall — FDA D-0552-2026
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
Overview of recall records associated with Eugia US LLC, including dates, categories and classifications where available.
Classification mix: Class II: 7, Class III: 1.
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
Failed Stability Specifications: Out of specification results for the Color Absorbance test during 12 Month sample analysis.
Out-of-Specification test results were obtained in at long term conditions during 3 month's stability study for related substances.
Out-of-Specification test results were obtained in at long term conditions during 3 month's stability study for related substances.
cGMP: complaints of crystals not redissolving into solution after warming and shaking the vials.
Presence of Particulate Matter: A market complaint was received of a glass piece in the vial.
CGMP Deviations
Presence of Particulate Matter: Complaint received of a glass particle in the vial.
This page summarizes recall records in which the official source identifies Eugia US LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.