ClearanceBrief
Recall Z-1302-2008 ยท DQY Catheter, Percutaneous

Boston Scientific Corporation

Boston Scientific Mach 1 peripheral Guide Catheter 6F, MP Multipurpose 90cm, .070 in (internal dia), Shaft lenght 90cm, Catalog Number: 19-626, UPN M001196260, Sterile EO, Availmed S.A. de C.V. (Mexico), Boston Scientific Corp., Maple Grove, MN 55311

DateMay 7, 2008 (initiated Feb 7, 2008)
StatusTerminated
ReasonMislabeled: Seven lots/ batches of Boston Scientific Mach 1 Guide Catheter may be mislabeled with the incorrect device length.
Root causeLabeling mix-ups
ActionConsignees were sent a Boston Scientific Urgent Voluntary Medical Device Recall letter on 2/7/08. The letter included the customer steps for recall, a complete listing of all product batches being recalled, the Reply Verification Tracking Form(s) and a return shipping label.
Quantity19
DistributionWorldwide Distribution including USA states of PA, AZ, NY, KY, CA, WV, OH, WA, MI, TN, IN, IL, NJ, KY, FL, AR, FL, NC, CO, TX, WV, WI, OR, AL, MN and ND and countries of BE, FR, GB, DE, IE, IT, JP, AU, SOUTH KOREA, NZ, TR, TW and ZA.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K0108746F MACH 1, MODEL 34356-XXX
Boston Scientific Corp, Jun 21, 2001
K0200286F MACH1/34356-XXX; 5F MACH1/35845-XXX; 7F MACH1/34357-XXX; 8F MACH1/34358-XXX
Boston Scientific, Jan 22, 2002