Published by Reclia Safety Desk | July 20, 2026
📌 Recall Notice
Product: Lidocaine 4% Topical Anesthetic Cream
Brand: Mohnark Pharmaceuticals Inc., of Davie, Fla.
Hazards: Chemical Risk
What to do: Stop using this product. Follow the recall instructions for refund or replacement.
Recall #9346 |
View original notice →
Recall Summary
| Product | Lidocaine 4% Topical Anesthetic Cream |
| Brand | Mohnark Pharmaceuticals Inc., of Davie, Fla. |
| Category | Toys Children |
| Recall Number | 9346 |
| Hazard | Chemical Risk |
| Units Affected | Not specified |
| Recall Date | June 30, 2022 |
| Remedy | Contact manufacturer |
| Country | 🇺🇸 United States |
Recall Information Record – Reclia Consumer Safety Database
Recall Summary
On June 30, 2022, Mohnark Pharmaceuticals Inc., of Davie, Florida, initiated a recall of its Lidocaine 4% Topical Anesthetic Cream. The recall was issued due to the product’s failure to meet the child-resistant packaging requirement under the Poison Prevention Packaging Act (PPPA). The recall number assigned by the U.S. Consumer Product Safety Commission (CPSC) is 22754. The recall alert was published on the CPSC website on June 30, 2022. No injuries have been reported in connection with this recall.
Affected Products
The recalled product is Mohnark Pharmaceuticals Lidocaine 4% Topical Anesthetic Cream. The product was sold in a white tube with a flip-top closure. The name “Mohnark Pharmaceuticals” is printed under a blue and green logo on the right side of the product tube. The lot code is located at the bottom of the product tube. The affected lot codes are: 01202201, 210201, 210301, 210503, 210505, 210601, 211002, and 210401. The Universal Product Code (UPC) for the product is 860002324906, located on the bottom side panel of the packaging. Approximately 9,000 units of the product are included in this recall. The product was manufactured in the United States. The cream was sold online at Amazon.com and Walmart.com from January 2021 through January 2022 for approximately $7.
Hazard Information
The recalled product contains lidocaine, a substance that must be packaged in child-resistant containers as required by the Poison Prevention Packaging Act (PPPA). The packaging of this product is not child resistant. This poses a risk of poisoning to young children if they ingest the anesthetic cream. No incidents or injuries have been reported to date.
Consumer Action Required
Consumers who have purchased the recalled Lidocaine 4% Topical Anesthetic Cream should immediately stop using the product. The product should be stored in a location that is out of sight and reach of children. Consumers must contact Mohnark Pharmaceuticals for instructions on how to properly dispose of the product. Mohnark Pharmaceuticals is contacting all known purchasers directly regarding this recall.
Official Remedy
The official remedy for this recall is a full refund. Consumers who follow the disposal instructions provided by Mohnark Pharmaceuticals will receive a full refund for the recalled product.
Contact Information
Consumers may contact Mohnark Pharmaceuticals toll-free at 866-611-5206 from 9 a.m. to 4 p.m. Eastern Time, Monday through Friday. Consumers may also visit the company’s website at www.mohnark.com and click on the “RECALL” link at the top of the page for additional information.

Recall Timeline
- **June 30, 2022** – Recall announced by CPSC (Source)
- **Current** – Consumers advised to stop using product
- **Ongoing** – Refund or replacement available
Frequently Asked Questions
Q: How do I identify the recalled Lidocaine 4% Topical Anesthetic Cream?
A: Check the model and serial number on your product against the official recall notice (#9346).
Q: What should I do if I own the recalled Lidocaine 4% Topical Anesthetic Cream?
A: The recall notice advises consumers to stop using the product and follow the recall instructions.
Q: How do I get a refund or replacement for the recalled Lidocaine 4% Topical Anesthetic Cream?
A: Contact the manufacturer using the information in the recall notice.
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Disclaimer: Information on this page is summarized from official recall notices.
Reclia is a recall information database and does not conduct product testing, safety certification,
or independent investigations.
Consumers should refer to the original recall notice
for complete details and official instructions.