Data Foundry

Drug recalls 2021

NovoLog — Class I drug recall D-0616-2021

Terminated recall by Novo Nordisk Inc, reported 2021-04-21, distributed nationwide. Temperature Abuse: product samples were stored at temperatures below 32* F which is not in accordance with sto

Recall numberD-0616-2021
Product typeDrug
ClassificationClass I
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmNovo Nordisk Inc, Plainsboro, NJ, United States
Recall initiated2021-03-22
Classified2021-06-10
Reported by FDA2021-04-21
Terminated2022-12-09
DistributedNationwide (US)
Reason classestemperature control
NDC00169-2001, 00169-2001-90, 00169-2100, 00169-2100-11, 00169-2101, 00169-2101-12, 00169-2101-25, 00169-3303, 00169-3303-12, 00169-3303-90, 00169-3303-91, 00169-6338, 00169-6338-10, 00169-6338-90, 00169-6338-97, 00169-6339, 00169-6339-10, 00169-6339-90, 00169-6339-97, 00169-6339-98, 00169-7501, 00169-7501-11, 00169-7501-90
Expiration dates2021-06-30, 2022-08-31

Product

NovoLog (Insulin aspart) Injection, 100 units/mL (U-100), One 10 mL multi-dose vial, Sample. Not for Resale, Rx Only, Manufactured by: Novo Nordisk A/S, Bagsvaerd, Denmark NDC 0169-7501-90

Reason for recall

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0616-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.