ClearanceBrief
Recall Z-1327-2018 ยท JLS Radioimmunoassay, Progesterone

Arrow International Inc

Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard Technology, Part Numbers: (1) ASK-45541-RWJ4; (2) ASK-45552-RWJ4

DateDec 22, 2017
StatusTerminated
ReasonCertain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot be guaranteed.
Root causeProcess control
ActionThe notification letter includes the following instructions for CUSTOMERS: 1. Discontinue use and quarantine any affected products. 2. Complete and return the Recall Acknowledgement Form to start return process. 3. Complete the Recall Acknowledgment Form if there is no product on hand. Instructions for DISTRIBUTORS: 1.Discontinue distribution and quarantine any affected products. 2. Communicate this recall to any customers with affected product. 3. Have the customers return any affected product to you with a completed Recall Acknowledgement Form. 4. Return affected products from inventory usin
DistributionDistributed in all 50 U.S. states and the District of Columbia. Distributed in Bahamas, Canada, Mexico, Panama, and Singapore.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K112896ARRW EVOLUTION
Arrow International (Subsidiary of Teleflex Inc.), May 10, 2012