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Class II: temporary or reversible health riskTerminated

KRS Global Biotechnology Nicotinamide Adenine Dinucleotide 500 mg Recall

Nicotinamide Adenine Dinucleotide 500 mg packaged in vials, Lyophilized-For IV Use, Rx…

KRS Global Biotechnology, Inc · Boca Raton, FL

Risk level
Class II
Reported by FDA
Jan 17, 2018
Recall ID
D-0185-2018
Check your lot numberHow we source this data

Summary

KRS Global Biotechnology recalled Nicotinamide Adenine Dinucleotide 500 mg starting Nov 16, 2017. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0185-2018 on Jan 17, 2018. Reason: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD) exceed the BUD/EXP of at least one ingredient used to make final product. Status: Terminated.

Why it was recalled

Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD) exceed the BUD/EXP of at least one ingredient used to make final product.

Product description

Nicotinamide Adenine Dinucleotide 500 mg packaged in vials, Lyophilized-For IV Use, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.

Lot numbers, UPCs & expiration codes

Lot: 06062017@3 BUD: 12/3/2017

Where it was sold

Nationwide in the USA, Bermuda, and New Zealand

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-0185-2018
Classification
Class II
Status
Terminated
Recall initiated
Nov 16, 2017
FDA report date
Jan 17, 2018
Quantity
2,535 vials
Recall type
Voluntary: Firm initiated
Recalling firm
KRS Global Biotechnology, Inc

Original FDA data

Every field from FDA enforcement report D-0185-2018, exactly as published.

Show all FDA fields
City
Boca Raton
State
FL
Status
Terminated
Country
United States
Event ID
78553
Address
791 Park of Commerce Blvd Ste 600
Code information
Lot: 06062017@3 BUD: 12/3/2017
Postal code
33487-3633
Report date
Jan 17, 2018
Product type
Drugs
Recall number
D-0185-2018
Classification
Class II
Recalling firm
KRS Global Biotechnology, Inc
Product quantity
2,535 vials
Termination date
May 11, 2020
Reason for recall
Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD) exceed the BUD/EXP of at least one ingredient used to make final product.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Nicotinamide Adenine Dinucleotide 500 mg packaged in vials, Lyophilized-For IV Use, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
Distribution pattern
Nationwide in the USA, Bermuda, and New Zealand
Recall initiation date
Nov 16, 2017
Initial firm notification
Letter
Center classification date
Jan 8, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0185-2018, published Jan 17, 2018. View the source record (openFDA) · FDA enforcement reports

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

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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