Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 0169-3204-90 recalled?

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Yes — this exact package was recalled

1 FDA recall names the code 0169-3204-90 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
insulin aspart injection
Strength
INSULIN ASPART 100 [iU]/mL
Form
Injection, Solution · Subcutaneous
Labeler
Novo Nordisk
Type
Human Prescription Drug
Product code
0169-3204

Recalls naming this package

Class I ยท High risk

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Temperature Abuse: product samples were stored at temperatures below 32* F which is not in accordance with storage requirements that could cause a lack of efficacy and damage to the cartridge and pen-injectors.

Terminated Temperature excursion Novo Nordisk Inc NDC 0169-3204-90 D-0611-2021

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