Class I · High risk
Lidocaine HCl Injection
Presence of Particulate Matter: The product was discolored and contained visible particulates (iron oxide) in the solution and embedded in the glass vial.
National Drug Code
Is NDC 0409-2066-05 recalled?
Lidocaine Hydrochloride · 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-2066-05) / 5 mL in 1 VIAL, SINGLE-DOSE (0409-2066-10)
Yes — this exact package was recalled
2 FDA recalls name the code 0409-2066-05 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.
- Active ingredient
- Lidocaine Hydrochloride
- Strength
- LIDOCAINE HYDROCHLORIDE 20 mg/mL
- Form
- Injection, Solution · Epidural, Infiltration, Intracaudal, Perineural
- Labeler
- Hospira, Inc.
- Type
- Human Prescription Drug
- Product code
- 0409-2066
Recalls naming this package
Class I · High risk
Lidocaine HCl Injection
Presence of Particulate Matter- Confimed customer complaint of particulates embedded in glass container and in contact with product solution.
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
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