Class II ยท Moderate risk
Brevibloc Premixed Injection
Presence of Particulate Matter: Complaints received of discolored solution identified as subvisible particles of iron oxide that are agglomerating.
National Drug Code
Is NDC 10019-0055-61 recalled?
Brevibloc · 10 BAG in 1 CARTON (10019-055-61) / 250 mL in 1 BAG
Yes — this exact package was recalled
1 FDA recall names the code 10019-0055-61 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
- Esmolol Hydrochloride
- Strength
- ESMOLOL HYDROCHLORIDE 10 mg/mL
- Form
- Injection · Intravenous
- Labeler
- Baxter Healthcare Company
- Type
- Human Prescription Drug
- Product code
- 10019-0055
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
- 10019-0075 Brevibloc 1
- 10019-0079 Bendamustine Hydrochloride 1
- 10019-0553 See recall 1
- 10019-0651 Sevoflurane 1
Free recall alerts
Know the day your medication is recalled
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