Class I · High risk
Bupivacaine Hydrochloride Inj.
Presence of particulate matter: Confirmed customer report for the presence of particulate matter within a single vial.
National Drug Code
Is NDC 0409-1159-02 recalled?
Bupivacaine Hydrochloride · 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-1159-02) / 30 mL in 1 VIAL, SINGLE-DOSE (0409-1159-19)
Yes — this exact package was recalled
2 FDA recalls name the code 0409-1159-02 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
- Bupivacaine Hydrochloride
- Strength
- BUPIVACAINE HYDROCHLORIDE 2.5 mg/mL
- Form
- Injection, Solution · Epidural, Infiltration, Intracaudal, Perineural
- Labeler
- Hospira, Inc.
- Type
- Human Prescription Drug
- Product code
- 0409-1159
Recalls naming this package
Class I · High risk
0.25% Bupivacaine HCl Injection
Presence of particulate matter: visible free floating and partially embedded particulate matter in the glass vials.
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
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.