FDAClass IIOctober 31, 2018

Lidocaine 1% + Epinephrine 1:100 recall: Subpotent

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 was Lidocaine 1% + Epinephrine 1:100 recalled?

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

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot# 04042018:58, Exp 10/17/18

Product
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
Recalling firm
RXQ Compounding LLC
Quantity
395 vials
Distribution
U.S.A. nationwide
Recall date
October 31, 2018
Classification
Class II
Status
Terminated
Agency
FDA (drug)
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