ClearanceBrief
Recall Z-2030-2018 ยท KGZ Accessories, Catheter

Arrow International Inc

Extension Line Slide Clamps; Product codes: SA-09847

DateApr 11, 2018
StatusTerminated
ReasonProduct sterility may be compromised due to unsealed packaging.
Root causeUnder Investigation by firm
ActionOn April 11, 2018 Arrow International mailed Urgent Medical Device Recall notifications to affected customers. Customers were instructed to take the following actions: 1. If you have affected stock, immediately discontinue use and quarantine any products with the product codes and lot numbers listed above, so that the affected products can be returned to Arrow. 2. To return product, complete the enclosed Recall Acknowledgement Form and fax it to 1-855-419-8507, Attn: Customer Service or email to recalls@teleflex.com. This will allow us to document the amount of product you have on hand for
Quantity416,055 total products
DistributionUS Nationwide, AUSTRALIA, AUSTRIA, BELGIUM, CANADA, CZECH REPUBLIC, DENMARK, ECUADOR, FRANCE, GERMANY, GREECE, HONG KONG, INDONESIA, IRELAND, ITALY, JAPAN, KOREA, NETHERLANDS, NEW ZEALAND, PANAMA, PHILIPPINES, POLAND, PUERTO RICO, ROMANIA, SAUDI ARABIA, SINGAPORE, SLOVENIA, SOUTH AFRICA, SPAIN, SWED
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.