Class II · Moderate risk
Lidocaine HCl Injection USP
Lack of Assurance of Sterility
National Drug Code
Is NDC 65282-1605-01 recalled?
Lidocaine Hydrochloride · 25 AMPULE in 1 CARTON (65282-1605-1) / 5 mL in 1 AMPULE
Yes — this exact package was recalled
1 FDA recall names the code 65282-1605-01 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 Anhydrous
- Strength
- LIDOCAINE HYDROCHLORIDE ANHYDROUS 10 mg/mL
- Form
- Injection, Solution · Epidural, Infiltration, Intracaudal, Perineural
- Labeler
- Spectra Medical Devices, LLC
- Type
- Human Prescription Drug
- Product code
- 65282-1605
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
- 65282-1510 Sodium Chloride 1
Free recall alerts
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