Blood Thinner Recall

Boehringer Ingelheim Pharmaceuticals, Inc., initiated a voluntary recall of DIPYRIDAMOLE Tablets USP, 75 mg, according to the latest US Food and Drug Administration Enforcement Report.

The ongoing recall includes 6400 100-count bottles that were distributed throughout the United States. The affected lot number is 554820 with an expiration date of May 2017.

The Class II recall was first initiated on October 6 after the presence of foreign tablets/capsules was detected.

The recall number is D-0114-2017.

—Meredith Edwards White

Reference

https://www.accessdata.fda.gov/scripts/ires/index.cfm