FDA recall record

Empower Clinic Services LLC dba Empower Pharmacy ASCORBIC ACID PRESERVED INJECTION SOLUTION recall — FDA D-0865-2023

Mislabeling: preservative free product labeled as preserved.

Class IIclassification
D-0865-2023official record ID
Jun 14, 2023report date

Recall record at a glance

Official recordD-0865-2023
CategoryDrug Recalls
ClassificationClass II
FDA record statusCompleted
Recalling firmEmpower Clinic Services LLC dba Empower Pharmacy
Report dateJun 14, 2023
Recall initiation dateMay 12, 2023
Quantity504 vials
LocationHouston, TX, United States

Official product description

ASCORBIC ACID PRESERVED INJECTION SOLUTION, 500 mg/mL, 30 mL Sterile Multiple-Dose Vial, RX ONLY, Compounded by: Empower Pharmacy, 5980 W Sam Houston Pkwy N Ste 300 Houston, TX 77041, NDC 72627-2405-1

Why the product was recalled

Mislabeling: preservative free product labeled as preserved.

Distribution information

Distributed 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: E-Mail.

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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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