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Class II: temporary or reversible health riskTerminated

Novo Nordisk Ozempic Recall

OZEMPIC (semaglutide) injection, 2 mg/1

Novo Nordisk Inc · Plainsboro, NJ

Risk level
Class II
Reported by FDA
Apr 21, 2021
Recall ID
D-0617-2021
Check your lot numberHow we source this data

Summary

Novo Nordisk recalled Ozempic starting Mar 22, 2021. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0617-2021 on Apr 21, 2021. Reason: 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. Status: Terminated.

Why it was recalled

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.

Product description

OZEMPIC (semaglutide) injection, 2 mg/1.5 mL (1.34 mg/mL) Prefilled pen, 1 pen, Sample. Not for Resale, Rx only, Novo Nordisk Inc, Plainsboro, NJ 08536, Manufactured by: Novo Nordisk A/S, Bagsvaerd, Denmark, NDC 0169-4132-90 (Pen), NDC 0169-4132-97 (Kit)

Lot numbers, UPCs & expiration codes

KP50867, exp 10/31/2022, KP53021, exp 04/30/2023, KP52338, exp 02/28/2023, JP54354, exp 08/31/2022, KP50676, exp 10/31/2022, KP51434, exp 11/30/2022, KP51491, exp 11/30/2022, KP51781, exp 01/31/2023, KP52249, exp 01/31/2023, KP52270, exp 01/31/2023, KP52722, exp 01/31/2023, KP52973, exp 01/31/2023, KP53031, exp 01/31/2023, KP53221, exp 12.04.2023, KP53369, exp 01/31/2023

Where it was sold

Nationwide in the USA

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0617-2021
Classification
Class II
Status
Terminated
Recall initiated
Mar 22, 2021
FDA report date
Apr 21, 2021
Quantity
N/A
Recall type
Voluntary: Firm initiated
Recalling firm
Novo Nordisk Inc

Original FDA data

Every field from FDA enforcement report D-0617-2021, exactly as published.

Show all FDA fields
City
Plainsboro
State
NJ
Status
Terminated
Country
United States
Event ID
87537
Address
800 Scudders Mill Rd
Code information
KP50867, exp 10/31/2022, KP53021, exp 04/30/2023, KP52338, exp 02/28/2023, JP54354, exp 08/31/2022, KP50676, exp 10/31/2022, KP51434, exp 11/30/2022, KP51491, exp 11/30/2022, KP51781, exp 01/31/2023, KP52249, exp 01/31/2023, KP52270, exp 01/31/2023, KP52722, exp 01/31/2023, KP52973, exp 01/31/2023, KP53031, exp 01/31/2023, KP53221, exp 12.04.2023, KP53369, exp 01/31/2023
Postal code
08536-1606
Report date
Apr 21, 2021
Product type
Drugs
Recall number
D-0617-2021
Classification
Class II
Recalling firm
Novo Nordisk Inc
Termination date
Dec 9, 2022
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.
Voluntary / mandated
Voluntary: Firm initiated
Product description
OZEMPIC (semaglutide) injection, 2 mg/1.5 mL (1.34 mg/mL) Prefilled pen, 1 pen, Sample. Not for Resale, Rx only, Novo Nordisk Inc, Plainsboro, NJ 08536, Manufactured by: Novo Nordisk A/S, Bagsvaerd, Denmark, NDC 0169-4132-90 (Pen), NDC 0169-4132-97 (Kit)
Distribution pattern
Nationwide in the USA
Recall initiation date
Mar 22, 2021
Initial firm notification
Letter
Center classification date
Jun 10, 2021

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0617-2021, published Apr 21, 2021. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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