Class II · Moderate risk
Kit for the Preparation of Technetium Tc 99m Sestamibi Injection
Lack of Assurance of Sterility; Improper crimps on vials impacting the integrity of the product
National Drug Code
Is NDC 69945-0092-40 recalled?
Technetium Tc 99m Sestamibi · 30 VIAL in 1 CARTON (69945-092-40) / 10 mL in 1 VIAL
Yes — this exact package was recalled
1 FDA recall names the code 69945-0092-40 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
- Technetium Tc 99m Sestamibi
- Strength
- TETRAKIS(2-METHOXYISOBUTYLISOCYANIDE)COPPER(I)…
- Form
- Injection · Intravenous
- Labeler
- Curium US LLC
- Type
- Human Prescription Drug
- Product code
- 69945-0092
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.
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.