American Regent Voluntarily Recalls All Lots of Ketorolac Tromethamine Injection

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Title: American Regent Voluntarily Recalls All Lots of Ketorolac Tromethamine Injection

American Regent Voluntarily Recalls All Lots of Ketorolac Tromethamine Injection
Wed, 21 Oct 2009 10:40:00 -0500

This voluntary recall is due to the potential that particulate matter in conjunction with crystallization may be present in the product. This recall does not include other concentrations of AMERICAN REGENT Ketorolac Tromethamine Injection, USP.

Firm Press Release: FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.


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