RecallHawk

Lidocaine 4% Topical Anesthetic Cream

Mohnark Pharmaceuticals Inc., of Davie, Fla.

Summary

CPSC recall: Lidocaine 4% Topical Anesthetic Cream. By Mohnark Pharmaceuticals Inc., of Davie, Fla.. Hazard: The product contains lidocaine which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging is not child resistant, posing a risk of poisoning to young children if they ingest the anesthetic cream.. Remedy: Consumers should immediately stop using the recalled cream and store it in a location out of sight and reach of children. Contact

Details

Source

CPSC Consumer Product Recall

External ID

9346

Action Date

2022-06-30

Status

Recalled

Category

consumer_product

Product Description

The recall involves Mohnark Pharmaceuticals Lidocaine 4% Topical Anesthetic Cream. The product was sold in a white tube

Context & Analysis

This is a unclassified recall.

This was one of 12 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Mohnark Pharmaceuticals Inc., of Davie, Fla. has 2 FDA actions in our database, including 1 recall.

Frequently Asked Questions

What is a FDA recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Mohnark Pharmaceuticals Inc., of Davie, Fla.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Mohnark Pharmaceuticals Inc., of Davie, Fla. have FDA actions?

Mohnark Pharmaceuticals Inc., of Davie, Fla. has 2 FDA actions in our database, including 1 recall and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "9346" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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