FDA recall, , Low risk
Enovachem Pharmaceuticals Lidolog Kit
The Lidolog Kit has a label that covers the barcode, making it hard to scan.
Summary by Recall Canary from the FDA notice
What happened
Asclemed USA Inc., of Torrance, California, recalled 18 kits of the Lidolog Kit, which contains Lidocaine HCl Injection, USP, 2% (2mL) vial, 1 Dose, Single use Only, Rx Only, distributed by Enovachem Pharmaceuticals, Torrance, CA 90501. The recall began July 15, 2026, and was added to the FDA's Enforcement Report on July 20, 2026, with the agency classifying it that same day.
The reason for the recall is that the label wrap covers the barcode, making it hard to scan. The product was distributed in Tennessee.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medicine recalls:
- Check the FDA or company notice for instructions specific to this product.
- Ask your pharmacist or doctor whether your lot is affected and what to do.
Is your kit affected?
Match the NDC and lot code listed under your product.
An NDC (National Drug Code) is usually printed on the drug's label.
Lidolog Kit
- NDC
- 76420-760-01
- Lot code
- 070126X1
Recall details
- Company began the recall
- Sold in
Within U.S. - Tennessee
- Company
- Asclemed USA Inc.Torrance, California
- Hazard
- Labeling error
- Risk
Low risk
Taking it is unlikely to cause health problems.
FDA Class III recall · How risk is rated
- Event ID
- 99408
- Recall number
- D-0713-2026
- Quantity recalled
- 18 kits
All recalls from Asclemed USA Inc.
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
