Reported May 15, 2019 · Terminated

Mycophenolate Mofetil for Injection, USP 500 mg, 4 Single Dose Vials, Rx Only, Distributed by: Par Pharmaceutical…

Par Pharmaceutical, Inc.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Par Pharmaceutical, Inc. · 1 Ram Ridge Rd · Chestnut Ridge, NY · 10977-6714

Is this the product you have?

  • Mycophenolate Mofetil for Injection, USP 500 mg, 4 Single Dose Vials, Rx Only
  • Distributed byPar Pharmaceutical Chestnut Ridge, NY 10977 NDC 342023-172-044
Lot codes and dates
    • AD812
    • exp 9/2020
Amount recalled
4506 packs

Where it was sold

  • Nationwide

Why it was recalled

Stop using this product now

Presence of Particulate Matter; glass fragment observed in one vial of reconstituted product

Using this product could cause serious injury, illness or death — stop using it now.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Par Pharmaceutical, Inc. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Jun 20, 2023 · Data as of Sep 19, 8:05 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.