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Class I: serious health riskTerminated

Mylan Institutional CARBOplatin Injection 450 mg/45 mL Recall

CARBOplatin Injection 450 mg/45 mL (10 mg/mL), 45 mL packaged in a 100 mL Multi-Dose Vi…

Mylan Institutional LLC · Rockford, IL

Risk level
Class I
Reported by FDA
Aug 26, 2015
Recall ID
D-1331-2015
Check your lot numberHow we source this data

Summary

Mylan Institutional recalled CARBOplatin Injection 450 mg/45 mL starting Mar 18, 2015. The FDA classified it as Class I (serious health risk) and published enforcement report D-1331-2015 on Aug 26, 2015. Reason: Presence of Particulate Matter. Status: Terminated.

Why it was recalled

Presence of Particulate Matter

Product description

CARBOplatin Injection 450 mg/45 mL (10 mg/mL), 45 mL packaged in a 100 mL Multi-Dose Vial, Rx only, Manufactured for: Mylan Institutional LLC, Rockford, IL 61103, Made in India, NDC 67457-493-46, UPC 3 67457 49346 6.

Lot numbers, UPCs & expiration codes

Lot #: 7801312, Exp 06/15

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-1331-2015
Classification
Class I
Status
Terminated
Recall initiated
Mar 18, 2015
FDA report date
Aug 26, 2015
Quantity
4,445 vials
Recall type
Voluntary: Firm initiated
Recalling firm
Mylan Institutional LLC

Original FDA data

Every field from FDA enforcement report D-1331-2015, exactly as published.

Show all FDA fields
City
Rockford
State
IL
Status
Terminated
Country
United States
Event ID
70991
Address
4901 Hiawatha Dr
Code information
Lot #: 7801312, Exp 06/15
Postal code
61103-1287
Report date
Aug 26, 2015
Product type
Drugs
Recall number
D-1331-2015
Classification
Class I
Recalling firm
Mylan Institutional LLC
Product quantity
4,445 vials
Termination date
May 19, 2016
Reason for recall
Presence of Particulate Matter
Voluntary / mandated
Voluntary: Firm initiated
Product description
CARBOplatin Injection 450 mg/45 mL (10 mg/mL), 45 mL packaged in a 100 mL Multi-Dose Vial, Rx only, Manufactured for: Mylan Institutional LLC, Rockford, IL 61103, Made in India, NDC 67457-493-46, UPC 3 67457 49346 6.
Distribution pattern
Nationwide
Recall initiation date
Mar 18, 2015
Initial firm notification
Letter
Center classification date
Aug 14, 2015

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1331-2015, published Aug 26, 2015. 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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