Teleflex Medical Pilling(R) Coronary Scissors, 45Deg 7", Catalog numbers: 352165, Teleflex Medical, Research Triangle Park, NC 27709 Recall

Check Your Product

According to the U.S. Food and Drug Administration (FDA)

Reason for Recall

As stated by FDA

The product has a rough square finish instead of a smooth rounded finish which can cause damage to arteries.

Recommended Action

Per FDA guidance

Consignees were notified by an Urgent Medical Device Recall letter, dated 03/03/2009, via UPS Next Day. Hospitals were instructed to immediately discontinue use of the products, inspect the scissors for the date codes and to return the product to Teleflex Medical for replacement. Distributors were instructed to forward the letter to their consignees to retrieve relevant product from those locations. A Recall Acknowledgement Form was attached to be completed and faxed back to Teleflex Medical. A second mailing to non-responding customers on the consignee list will be made approximately four to six weeks after the first mailing. A third mailing to non-responding customers on the consignee list will be made approximately four to six weeks after the second mailing or they may be contacted by phone, e-mail or fax. A record of these contacts will be maintained. Affected product retrieved by Teleflex Medical will be destroyed and replacement product provided to the consignee. Records of destruction will be maintained.

Distribution

As reported by FDA

AL, AZ, CA, CO, DE, FL, IN, IA, KS, MD, MA, MI, MS, MO, NV, NH, NJ, NY, OH, OK, OR, PA, RI, TN, TX, UT, WA, DC