Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 50227-1030-05 recalled?

Lidocaine · 50 CARTRIDGE in 1 CARTON (50227-1030-5) / 1.7 mL in 1 CARTRIDGE

Yes — this exact package was recalled

1 FDA recall names the code 50227-1030-05 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

1 of these recalls is still ongoing.

Active ingredient
Lidocaine Hydrochloride and Epinephrine Bitartrate
Strength
LIDOCAINE HYDROCHLORIDE 20 mg/mL; EPINEPHRINE BITARTRATE…
Form
Injection, Solution · Submucosal
Labeler
Patterson Dental
Type
Human Prescription Drug
Product code
50227-1030

Recalls naming this package

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.

Other recalled products from this labeler

  • 50227-1002 Patterson Dental Topical Anesthetic 1