FDA recall record

Denver Solutions, LLC DBA Leiters Health Lidocaine HCL 1% (10mg/mL), PHENYLephrine HCL 1.5% recall — FDA D-0363-2024

Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination.

Class IIclassification
D-0363-2024official record ID
Mar 6, 2024report date

Recall record at a glance

Official recordD-0363-2024
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmDenver Solutions, LLC DBA Leiters Health
Report dateMar 6, 2024
Recall initiation dateFeb 20, 2024
Quantity40,890 vials
LocationEnglewood, CO, United States

Official product description

Lidocaine HCL 1% (10mg/mL), PHENYLephrine HCL 1.5% (15mg/mL), 1 ml in a Single- Dose Vial, RX Only, Leiters 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-090-42

Why the product was recalled

Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination.

Distribution information

Nationwide in the USA

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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