Class I ยท High risk
Bleomycin for Injection
Presence of particulate matter: glass
National Drug Code
Is NDC 61703-0332-18 recalled?
Bleomycin · 1 VIAL, SINGLE-DOSE in 1 CARTON (61703-332-18) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE
Yes — this exact package was recalled
1 FDA recall names the code 61703-0332-18 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
- Bleomycin
- Strength
- BLEOMYCIN SULFATE 15 [USP'U]/1
- Form
- Injection, Powder, Lyophilized, for Solution · Intramuscular, Intrapleural, Intravenous, Subcutaneous
- Labeler
- Hospira, Inc.
- Type
- Human Prescription Drug
- Product code
- 61703-0332
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
- 61703-0339 Carboplatin 4
- 61703-0360 Carboplatin 3
- 61703-0303 Cytarabine 1
- 61703-0327 See recall 1
- 61703-0342 Paclitaxel 1
- 61703-0343 Mitoxantrone 1
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