Class II ยท Moderate risk
Venofer (iron sucrose)
Presence of Particulate Matter: Potential for glass delamination from the vials.
National Drug Code
Is NDC 49230-0530-25 recalled?
Venofer · 25 VIAL, SINGLE-DOSE in 1 TRAY (49230-530-25) / 2.5 mL in 1 VIAL, SINGLE-DOSE (49230-530-01)
Yes — this exact package was recalled
1 FDA recall names the code 49230-0530-25 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
- iron sucrose
- Strength
- IRON SUCROSE 20 mg/mL
- Form
- Injection, Solution · Intravenous
- Labeler
- Fresenius Medical Care Holdings, Inc.
- Type
- Human Prescription Drug
- Product code
- 49230-0530
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
- 49230-0300 Sodium Chloride 5
- 49230-0206 Delflex 4
- 49230-0209 Delflex 3
- 49230-0212 Delflex 3
- 49230-0188 Delflex 1
- 49230-0534 Venofer 1
Free recall alerts
Know the day your medication is recalled
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