Skip to content
Recall Observatory FDA recall evidence

Device product

Atlantis PV, 8.5F, 15 MHz Peripheral Imaging Catheter: Sterile, R; Sterilized using irradiation. Product Usage: This catheter is a 15 MHz ultrasound imaging catheter intended to operate with an IVUS instrument for diagnostic imaging. It is used with an 8.5F-introducer sheath and a 0.035 guidewire.

Z-0900-2014

January 06, 2014

Class II

Product summary

Firm
Boston Scientific Corporation
Event
Event 67298
Status
Terminated
Classification
Class II
Quantity
1068 single units
Official record key
device-enforcement:Z-0900-2014

Official wording

Reason: Reports of physicians experiencing inability to pass a 0.035" guidewire through the guidewire lumen and exit port at the (proximal) Y-manifold of the imaging catheter.

Code information: Product number: H749364560, Catalog number: 36456; Lot numbers: 16159358, 16183964, 16230195, 16230673, 16247263, 16257809, 16268498, 16289177, 16311356, 16330543, 16342824, 16419885, 16420624, 16420903, 16447744, 16458536, 16486133, 16494530; Expiration Date: June 11th 2014 to October 29th 2014.

Distribution pattern: US Nationwide Distribution and Mexico

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Reports of physicians experiencing inability to pass a 0.035" guidewire through the guidewire lumen and exit port at the (proximal) Y-manifold of the imaging catheter.