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Novo Nordisk Inc. recalls

Every recall we track for Novo Nordisk Inc. — 18 in all, from 2016–2025 — plus the complaints and injury reports the public filed about them. 2 are rated “stop using now”.

18recalls
139complaints & reports
96injuries reported
28deaths reported

Recalls per year, by danger level

Recalls from Novo Nordisk Inc. peaked in 2021 (13); 16 since 2017. 6% rated “stop using now”.

2017: 1 recall — 1 use caution120172018: 0 recalls20182019: 0 recalls20192020: 0 recalls20202021: 13 recalls — 13 lower risk1320212022: 0 recalls20222023: 0 recalls20232024: 0 recalls20242025: 2 recalls — 1 stop using now, 1 use caution220252026 (to date): 0 recalls2026to date

All FDA recall records for Novo Nordisk Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.

Recalls per year for Novo Nordisk Inc., by danger level
YearStop using nowUse cautionLower riskNot yet ratedTotal
201701001
201800000
201900000
202000000
20210013013
202200000
202300000
202400000
202511002
2026 (to date)00000

Novo Nordisk Inc. recalls before 2017

Recalls on record by year.

  • 20162

Most common reasons for Novo Nordisk Inc. recalls

  • Presence of Particulate Matter: Hair was found in a prefilled syringe2

What to do if you have a recalled Novo Nordisk Inc. product

  1. Match the NDC and lot number on your bottle or box to the recall.
  2. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first.
  3. Report side effects to FDA MedWatch.

See this week’s new recalls.

All Novo Nordisk Inc. recalls

5 shown

Novo Nordisk Inc. recall questions

How many recalls has Novo Nordisk Inc. had?

18 recalls from Novo Nordisk Inc. are on record with U.S. safety agencies, from 2016–2025 (17 drug, 1 medical device).

What is the most recent Novo Nordisk Inc. recall?

Novo Nordisk Inc. recalls Wegovy (semaglutide) Injection, 1 mg/0.5 mL, 4 Single-Dose Prefilled Pens, Manufactured by: Novo Nordisk A/S, DK-2880, dated Dec 19, 2025. Every Novo Nordisk Inc. recall is listed on this page, newest first.

Why are Novo Nordisk Inc. products recalled?

The most common reasons on record: Presence of Particulate Matter: Hair was found in a prefilled syringe (2).

What should I do if I have a recalled Novo Nordisk Inc. product?

Match the NDC and lot number on your bottle or box to the recall. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first. Report side effects to FDA MedWatch.

How do I get alerts for new Novo Nordisk Inc. recalls?

Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.