NOVO NORDISK INC.
1 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (1)
Registered facilities (5)
- NOVO NORDISK A/S - NEEDLE MANUFACTURING AND SOURCI FEI 3004547341 · DK
- NOVO NORDISK INC. FEI 2244771 · NJ
- NOVO NORDISK A/S FEI 3003131673 · DK
- Novo Nordisk (China) Pharmaceuticals, Co. Ltd. FEI 3005186124 · CN
- NOVO NORDISK A/S FEI 3002807751 · DK
Recalls & enforcement
- Class IITerminated2017-07-05A small number of batches may crack or break if exposed to certain chemicals, like certain cleaning agents.
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “NOVO NORDISK INC. — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-9027307-novo-nordisk-inc/
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