Mohnark Pharmaceuticals Recalls Lidocaine Topical Anesthetic Cream Due to Failure to Meet Child-Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
Recall at a glance
- Recall number
- 22-754 (CPSC)
- Recall date
- June 30, 2022
- Brand
- Mohnark Pharmaceuticals
- Category
- Other consumer products
- Products
- Lidocaine 4% Topical Anesthetic Cream
- Hazard
- Failure to Meet Child-Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
- Hazard type
- Choking and ingestionPoisoning and toxic substances
- Remedy
- Refund
- Units
- About 9,000
- Made in
- United States
- Last updated by CPSC
- June 30, 2022
What was recalled
The recall involves Mohnark Pharmaceuticals Lidocaine 4% Topical Anesthetic Cream. The product was sold in a white tube with a flip-top closure. Mohnark Pharmaceuticals is printed under the 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 UPC 860002324906 is located on bottom side panel of the packaging.
Is my product affected?
Compare your product with the details below, including model numbers where listed.
- Lidocaine 4% Topical Anesthetic Cream · About 9,000 units
Photos from the recall notice


Where it was sold
Companies named in the notice: Online at Amazon.com and Walmart.com from January 2021 through January 2022 for about $7.; Mohnark Pharmaceuticals Inc., of Davie, Fla..
Consumer contact
Mohnark Pharmaceuticals toll-free at 866-611-5206 from 9 a.m. to 4 p.m. ET Monday through Friday, or online at www.mohnark.com and click on "RECALL" at the top of the page for more information.
Recall history and context
Since 2019 CPSC has recorded 399 recalls in the other consumer products category, 68 recalls of them in the past 12 months.
Frequently asked questions
What was recalled?
Lidocaine 4% Topical Anesthetic Cream (About 9,000 units). The recall involves Mohnark Pharmaceuticals Lidocaine 4% Topical Anesthetic Cream.
Why was it recalled?
CPSC lists the reason as: Failure to Meet Child-Resistant Packaging Requirement; Risk of Poisoning (Recall Alert).
What should I do if I own one?
Consumers should immediately stop using the recalled cream and store it in a location out of sight and reach of children. Contact Mohnark Pharmaceuticals for instructions on how to dispose of the product to receive a full refund. Mohnark Pharmaceuticals is contacting all known purchasers directly.
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Source: U.S. Consumer Product Safety Commission recall data, shown as published and last updated by CPSC on June 30, 2022. Details can change; the official notice is the authority. If your product may be recalled, stop and read the notice before deciding what to do. Terms and disclaimer.