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Class I: serious health riskTerminated

Bracco Diagnostic Isovue -370 Recall

Isovue -370 (Iopamidol) Injection 76%, Prefilled 10 x 75 mL (NDC 0270-1316-66), 10 x 10…

Bracco Diagnostic Inc · Monroe Township, NJ

Risk level
Class I
Reported by FDA
Feb 13, 2013
Recall ID
D-157-2013
Check your lot numberHow we source this data

Summary

Bracco Diagnostic recalled Isovue -370 starting Nov 21, 2012. The FDA classified it as Class I (serious health risk) and published enforcement report D-157-2013 on Feb 13, 2013. Reason: Presence of Particulate Matter; fibers identified as cellulose and polyvinyl. Status: Terminated.

Why it was recalled

Presence of Particulate Matter; fibers identified as cellulose and polyvinyl

Product description

Isovue -370 (Iopamidol) Injection 76%, Prefilled 10 x 75 mL (NDC 0270-1316-66), 10 x 100 mL (NDC 0270-1316-67), 10 x 125 mL (NDC 0270-1316-68) Power Injector Syringe, Rx Only, Manufactured for Bracco Diagnostics Inc., Princeton, NJ 08543 by Nycomed GmbH 78224 Singen (Germany).

Lot numbers, UPCs & expiration codes

Lot #: 9K37791, Exp 11/12; 9L40746, Exp 12/12; 0A43705, Exp 01/13; 0C57509, 0C57521, Exp 03/13; 0E62913, Exp 05/13

Where it was sold

Nationwide.

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-157-2013
Classification
Class I
Status
Terminated
Recall initiated
Nov 21, 2012
FDA report date
Feb 13, 2013
Quantity
5483 syringes (548.3 boxes)
Recall type
Voluntary: Firm initiated
Recalling firm
Bracco Diagnostic Inc

Original FDA data

Every field from FDA enforcement report D-157-2013, exactly as published.

Show all FDA fields
City
Monroe Township
State
NJ
Status
Terminated
Country
United States
Event ID
63765
Address
259 Prospect Plains Road
Address (line 2)
Building H
Code information
Lot #: 9K37791, Exp 11/12; 9L40746, Exp 12/12; 0A43705, Exp 01/13; 0C57509, 0C57521, Exp 03/13; 0E62913, Exp 05/13
Postal code
08831
Report date
Feb 13, 2013
Product type
Drugs
Recall number
D-157-2013
Classification
Class I
Recalling firm
Bracco Diagnostic Inc
Product quantity
5483 syringes (548.3 boxes)
Termination date
Jul 6, 2015
Reason for recall
Presence of Particulate Matter; fibers identified as cellulose and polyvinyl
Voluntary / mandated
Voluntary: Firm initiated
Product description
Isovue -370 (Iopamidol) Injection 76%, Prefilled 10 x 75 mL (NDC 0270-1316-66), 10 x 100 mL (NDC 0270-1316-67), 10 x 125 mL (NDC 0270-1316-68) Power Injector Syringe, Rx Only, Manufactured for Bracco Diagnostics Inc., Princeton, NJ 08543 by Nycomed GmbH 78224 Singen (Germany).
Distribution pattern
Nationwide.
Recall initiation date
Nov 21, 2012
Initial firm notification
Letter
Center classification date
Feb 7, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-157-2013, published Feb 13, 2013. View the source record (openFDA) · FDA enforcement reports

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

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