Class II · Moderate risk
Draximage MAA
Lack of Assurance of Sterility: Out-of-specification test results obtained for Endotoxin testing.
National Drug Code
Is NDC 65174-0270-30 recalled?
Draximage Maa · 30 INJECTION, POWDER, FOR SOLUTION in 1 KIT (65174-270-30)
Yes — this exact package was recalled
1 FDA recall names the code 65174-0270-30 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
- Kit for the preparation of Technetium Tc 99m Albumin aggregated
- Strength
- ALBUMIN AGGREGATED 2.5 mg/1
- Form
- Injection, Powder, for Solution · Intravenous
- Labeler
- Jubilant DraxImage Inc
- Type
- Human Prescription Drug
- Product code
- 65174-0270
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
- 65174-0179 Kit for the Preparation of Technetium Tc 99m Sulfur Colloid 1
- 65174-0288 Draximage Dtpa 1
- 65174-0461 Sodium Iodide I 131 Diagnostic 1
Free recall alerts
Know the day your medication is recalled
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