Teligent Pharma recalls 4% Lidocaine Hydrochloride topical solution (50mL bottles) due to superpotent drug risk. This prescription medication may cause serious injury if misused.
Superpotent Drug: Minimally superpotent
Teligent Pharma is recalling 4% lidocaine topical solution (50mL bottles) because it's classified as a superpotent drug. This means it could cause serious injury if used incorrectly or inappropriately.
The product is classified as a superpotent drug, meaning it has a high risk of causing serious injury if misused. This classification indicates the medication could be dangerous even with proper use, though the exact mechanism isn't specified in the recall.
Prescription drug users who have the 50mL bottles labeled as 4% lidocaine hydrochloride topical solution. People with medical conditions requiring lidocaine may be at higher risk.
Check for 50mL screw cap bottles labeled 'Lidocaine Hydrochloride, Topical Solution USP, 4% (40 mg/mL)' with the NDC code 63739-997-64. This product was distributed by McKesson Corporation and manufactured in Buena, NJ.
Look for the product label indicating 50mL bottles of 4% lidocaine hydrochloride topical solution with NDC 63739-997-64.
The recall states it's a superpotent drug, which means it could cause serious injury if misused. The official notice does not specify if it's safe to use.
The recall does not provide a remedy, so the official notice does not specify what to do with the product.
Check for 50mL screw cap bottles labeled 'Lidocaine Hydrochloride, Topical Solution USP, 4% (40 mg/mL)' with NDC 63739-997-64.
We’ve drafted a message you can send Teligent Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0296-2022 — Teligent Pharma Teligent Pharma Hello, I own a Teligent Pharma that is covered by recall D-0296-2022 from Teligent Pharma. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
