FDA recall record

RXQ Compounding Lidocaine 1% + Epinephrine 1:100,000 (MDV) INJ SOL, 50 mL per glass vial recall — FDA D-0130-2019

Subpotent drug: During testing of the retention sample, the firm discovered that the product was sub-potent.

Class IIclassification
D-0130-2019official record ID
Oct 31, 2018report date

Recall record at a glance

Official recordD-0130-2019
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmRXQ Compounding LLC
Report dateOct 31, 2018
Recall initiation dateSep 25, 2018
Quantity395 vials
LocationAthens, OH, United States

Official product description

Lidocaine 1% + Epinephrine 1:100,000 (MDV) INJ SOL, 50 mL per glass vial, Rx only, 340 West State Street, Unit 9, Athens, OH 45701. NDC 7073197450

Why the product was recalled

Subpotent drug: During testing of the retention sample, the firm discovered that the product was sub-potent.

Distribution information

U.S.A. nationwide

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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