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Recall Observatory FDA recall evidence

Device product

Boston Scientific ACUITY Pro Coronary Sinus Guide Catheter, 9 Fr. Model 8104, 8105, 8106, 8107, 8108, 8109, 8110, 8111, 8112, 8113, 8114, 8115, 8116, 8117, 8118, and 8119. The ACUITY Pro Lead Delivery System is designed for venous use to aid in the selective placement of cardiac resynchronization therapy (CRT) implantable venous leads in the cardiac vasculature. The catheter shafts are comprised of a PTFE inner liner, a reinforcing layer of stainless steel braid, and an outer polymer jacket. The distal end has a radiopaque polymer tip, while the proximal end has a hub with flush luer fitting to allow flush, contrast injection and aspiration polymer .

Z-0588-2016

November 25, 2015

Class II

Product summary

Firm
Boston Scientific Corporation
Event
Event 72739
Status
Terminated
Classification
Class II
Quantity
900 units
Official record key
device-enforcement:Z-0588-2016

Official wording

Reason: Potential for separation of the proximal handle from the shaft.

Code information: Model 8104, Lots: 18279548, 18279734, 18324877, 18329863, 18330946, 18348755, 18351569, 18353214, 18426640, 18461104, 18461521. Model 8105, Lots: 18281110, 18315176, 18322343, 18323156, 18323651, 18324468, 18327210, 18327359, 18345738, 18346540, 18346668, 18347522, 18352159, 18354329, 18379847, 18380498, 18393785, 18394034, 18395315, 18408497, 18408902, 18410018, 18428314, 18435809, 18437015, 18437680, 18439474, 18440388, 18444811, 18445630, 18446236, 18462103, 18462459, 18463154, 18466449, 18478544. Model 8106, Lots: 18286550, 18410783. Model 8107, Lots: 18285401, 18285605, 18312411, 18312981, 18313754, 18337534, 18338037, 18354248, 18411116, 18413022, 18413155, 18413834. Model 8108, Lots: 18273724, 18284294, 18338159, 18414856. Model 8109, Lots: 18285220, 18293137, 18294062, 18313856, 18314250, 18332118, 18337848, 18353117, 18415202, 18415923, 18416945, 18418278, 18419899. Model 8110, Lots: 18421013, 18473202. Model 8111, Lots: 18285930, 18351033, 18353540, 18420652, 18468909 . Model 8112, Lots: 18291473, 18336768, 18355225, 18421690, 18427953. Model 8113, Lots: 18324876, 18324963, 18332278, 18352696, 18358192, 18371973, 18372577, 18440783, 18441697, 18467134, 18468171, 18471598, 18472178, 18478892, 18479477. Model 8114, Lots: 18282143, 18284604, 18335173, 18345117, 18441212, 18442550, 18442887. Model 8115, Lots: 18288704, 18328790, 18329233, 18356691, 18357371, 18357372, 18372837, 18373201, 18377504, 18378867, 18446665, 18447045, 18451382, 18451950, 18452785, 18453099, 18464410, 18473932, 18477470, 18483223, 18483940. Model 8116, Lots: 18281865, 18473055. Model 8117, Lots: 18333920, 18334332, 18466601. Model 8118, Lots: 18316161, 18336837, 18348081. Model 8119, Lots: 18286265, 18291252, 18332911, 18336838, 18347898, 18480844, 18483020, 18471580.

Distribution pattern: Worldwide Distribution - US (nationwide) and Internationally to Argentina, Australia, Austria, Belgium, Colombia, Cyprus, Czech Republic, Egypt, Finland, France, Germany, Great Britain, Greece, Hong Kong, Ireland, Italy, Japan, Malaysia, Netherlands, Poland, Portugal, Serbia, Singapore, Slovenia, Spain, Sweden, Switzerland, and Thailand.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Potential for separation of the proximal handle from the shaft.