CLASS I ONGOING Drug recall · Reported 22 Sep 2021 · FDA Enforcement Report

Lidocaine Hydrochloride Topical Solution recalled by Teligent Pharma

Teligent Pharma is recalling Lidocaine Hydrochloride Topical Solution, USP, 4%, distributed nationwide in the US. The recall was initiated on 3 Aug 2021 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot #:14218, Exp. Date 08/2022
Quantity recalled32,544 glass bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0800-2021
FDA event ID
88454
Recalling firm
Teligent Pharma, Buena, NJ
Classification
Class I
Status
Ongoing
Recall initiated
3 Aug 2021
FDA classified
15 Sep 2021
Reported
22 Sep 2021
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Foreign Material
Drug class
Pain Medication

Timeline

3 Aug 2021Recall initiated by company
15 Sep 2021Classified by FDA+43 days
22 Sep 2021Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Superpotent Drug

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

Lidocaine Hydrochloride Topical Solution, USP, 4% , 50 mL glass bottles, Rx Only, Teligent Pharma Inc. Buena, New Jersey 08310, NDC 52565-009-50.

Where it was distributed

Nationwide within the United States and Canada

Nationwide

Questions about this recall

Is Lidocaine Hydrochloride Topical Solution, USP, 4% recalled?

Yes. Teligent Pharma recalled Lidocaine Hydrochloride Topical Solution, USP, 4% on 3 Aug 2021. The recall is Class I and its status is Ongoing. Recall number D-0800-2021.

Why was it recalled?

Superpotent Drug

Which lots are affected?

Lot #:14218, Exp. Date 08/2022

Where was it sold?

Nationwide within the United States and Canada

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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