Kirkman recalled 178 bottles of MAXIMUM Zone 1 4% Lidocaine Cream distributed nationwide in the U.S. by Dermal Source. The recall cites stability data that does not support the stated expiry date. Consumers and healthcare providers should stop using this product immediately and contact Kirkman for guidance.
Stability Data Does Not Support Expiry Date.
Consumers and healthcare providers should stop using this product immediately. Contact HTO Nevada Inc. dba Kirkman or your healthcare provider for guidance. Notification method: E-Mail
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MAXIMUM Zone 1 4% Lidocaine Cream is a topical anesthetic intended for minor skin procedures or analgesia in adults. Packaged in 1/2 oz bottles.
Stability data does not support the expiry date. Using expired lidocaine cream may result in reduced potency or unsafe outcomes.
This recall is not described as part of a broader industry pattern.
Consumers may experience reduced effectiveness or unknown safety risk if used past expiry date. Immediate suspension of use is advised.
Recall details available at the FDA enforcement report for D-0386-2026.
Not specified in the recall notice.
Keep the bottle, packaging, and recall notice. Save email communications with Kirkman.
Product: MAXIMUM Zone 1 4% Lidocaine Cream, 1/2 oz bottles. NDC: 80069-014. Lot #: 807CP-0003. Expiry date: 07/31/2026. Sold nationwide in the U.S. Distribution: Dermal Source, Portland, OR 97232. Quantity: 178 bottles.
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