ASAHI Corsair Pro XSRecalls & reported problems across all models

We found 2 models of ASAHI Corsair Pro XS by Asahi Intecc CO., Ltd. in the FDA's device registry (GUDID). Together they are named in 23 adverse event reports in the FDA's MAUDE database, received between Aug 19, 2020 and Dec 23, 2025 — classified as 1 death, 12 injuries, 10 malfunctions.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (7 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Most reported ASAHI Corsair Pro XS problems

ASAHI Corsair Pro XS models

2 models, most reported first. Each model has its own page with its reports, recalls and device details.

• ASAHI Corsair Pro XS CSR150-21S

  Catheter, percutaneous
  1 death13 reports
• ASAHI Corsair Pro XS CSR135-21S

  Catheter, percutaneous
  10 reports

Recent ASAHI Corsair Pro XS adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

• InjuryDec 23, 2025Material Separation; Material Separation

  IT WAS REPORTED THAT A PERCUTANEOUS CORONARY INTERVENTION (PCI) WAS PERFORMED FOR A CHRONIC TOTAL OCCLUSION (CTO) IN THE SEVERELY FIBROTIC AND HEAVILY CALCIFIED LEFT CIRCUMFLEX CORONARY ARTERY (LCX) WITH A Y-SHAPED ANASTOMOSIS OF VEIN GRAFT TIED IN. AN ASAHI SION BLUE GUIDE WIRE WAS ADVANCED TO THE ANASTOMOSIS OF VEIN GRAFT, FOLLOWED BY AN ASAHI CORSAIR PRO XS MICROCATHETER. WHEN THE CATHETER TIP REACHED THE ANASTOMOSIS, RESISTANCE WAS MET. THE PHYSICIAN TRIED TO ADVANCE THE MICROCATHETER BY TORQUEING FOR A VERY SHORT PERIOD OF TIME (LESS THAN 10 SECONDS), WHEN THE MICROCATHETERAND THE GUIDE WIRE FELT STUCK TO EACH OTHER. THE TWO DEVICES WERE REMOVED AS A UNIT. WHEN A DIFFERENT WORKHORSE GUIDE WIRE WAS ADVANCED TO THE ANASTOMOSIS OF VEIN GRAFT, SOME OBJECT WHICH LOOKED LIKE BALLOON RADIOPAQUE MARKERS WERE FOUND BETWEEN THE GRAFT MARKERS WERE OBSERVED FOR THE FIRST TIME UNDER ANGIOGRAPHY. WHEN THE REMOVED CORSAIR PRO XS MICROCATHETER AND SION BLUE GUIDE WIRE WERE EXAMINED, THE MICROCATHETER TIP APPEARED SLIGHTLY SHORTENED VISUALLY. UPON SLIGHT MANIPULATION OF THE TWO DEVICES, THE DISTAL TIP OF THE MICROCATHETER WAS FOUND LOOSENED. THE ANASTOMOSIS WAS PRE-DILATED, ANOTHER CORSAIR PRO

  Patient problems: Foreign Body In Patient

  MAUDE report 23874712 ↗
• InjuryDec 22, 2025Material Fragmentation; Physical Resistance/Sticking; Material Fragmentation; Physical Resistance/Sticking

  A SION BLUE WAS USED TO WIRE A VEIN GRAFT TIED IN TO THE LEFT CIRCUMFLEX. WHEN THE CORSAIR PRO XS WAS ADVANCED BEHIND THE WIRE, THERE WERE NO ISSUES UNTIL IT REACHED THE ANASTOMOSIS SITE AT THE TIP. AFTER MEETING RESISTANCE, WITHIN JUST A FEW SECONDS (<10S) OF TRYING TO TORQUE AND ADVANCE THE MICROCATHETER, THE OPERATOR COULD FEEL THAT IT HAD FUSED ONTO THE WIRE. ONCE THIS WAS REALIZED, THE WIRE AND MICROCATHETER WERE REMOVED AS A UNIT. THE MICROCATHETER WAS DISCARDED AND ANOTHER WORKHORSE WIRE WAS ADVANCED DOWN THE VEIN GRAFT. DURING THIS REWIRING UNDER LIVE FLUORO, WE NOTICED WHAT LOOKED LIKE BALLOON RADIOPAQUE MARKERS LOCATED BETWEEN THE GRAFT MARKERS THAT WEREN'T THERE BEFORE. PATIENT WAS UNDER ANESTHESIA WHEN EVENT OCCURRED AND WAS NOT AFFECTED BY THE PART OF THE DEVICE THAT WAS LEFT BEHIND IN THE VEIN GRAFT. THE PATIENT WAS ALSO HEMODYNAMICALLY STABLE BEFORE, DURING, AND AFTER THE PROCEDURE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23867401 ↗
• InjuryNov 17, 2025Insufficient Device Problem Information; Insufficient Device Problem Information

  IT WAS REPORTED THAT A PERCUTANEOUS CORONARY INTERVENTION (PCI) WAS PERFORMED FOR A MILDLY TORTUOUS AND MILDLY CALCIFIED CHRONIC TOTAL OCCLUSION (CTO) IN THE LEFT ANTERIOR DESCENDING ARTERY (LAD). AN ASAHI CORSAIR PRO XS MICROCATHETER AND AN ASAHI SION GUIDE WIRE WERE ADVANCED TO THE SEPTAL CHANNEL THROUGH THE #4 POSTERIOR DESCENDING (PD) BRANCH VIA RETROGRADE APPROACH. THE SION GUIDE WIRE WAS EXCHANGED TO AN ASAHI SUOH 03 GUIDE WIRE AND THE SUOH 03 GUIDE WIRE COULD BE ADVANCED TO THE LAD. ALTHOUGH THE CORSAIR PRO XS MICROCATHETER COULD NOT BE ADVANCED AT FIRST, THE CORSAIR PRO XS MICROCATHETER COULD BE ADVANCED WITH THE SUPPORT OF A NIPRO 5FR GUIDE PLUS GUIDING CATHETER. USING THE RETROGRADE GUIDE WIRE AS A MARKER, AN ASAHI SASUKE DOUBLE LUMEN CATHETER AND AN ASAHI CONQUEST PRO 12 ST GUIDE WIRE WERE ADVANCED VIA ANTEGRADE APPROACH, BUT THEY COULD NOT CROSS THE LESION. THE GUIDE WIRE WAS CHANGED TO AN ASAHI GLADIUS GUIDE WIRE, TO AN ASAHI GAIA NEXT 4 GUIDE WIRE AND FINALLY TO AN ASAHI CONQUEST PRO 8-20 GUIDE WIRE. THE CONQUEST PRO 8-20 GUIDE WIRE CROSSED THE LESION. WHEN THE RETROGRADE SION GUIDE WIRE WAS REMOVED AFTER PERFORMING REVERSE CART TECHNIQUE, PERFORATION WAS OBSERVED IN

  Patient problems: Perforation of Vessels

  MAUDE report 23566081 ↗
• InjuryJan 14, 2025Material Separation; Material Separation

  IT WAS REPORTED THAT A PERCUTANEOUS CORONARY INTERVENTION (PCI) FOR A CHRONIC TOTAL OCCLUSION (CTO) LESION IN SEGMENTS #1-3 OF THE RIGHT CORONARY ARTERY (RCA) WAS PERFORMED BY THE RETROGRADE APPROACH WITH A FINECROSS MICROCATHETER (TERUMO) AND AN ASAHI SUOH 03 GUIDE WIRE BY WAY OF THE FIRST SEPTAL BRANCH. AS A STENT HAD BEEN ALREADY DEPLOYED, THE FINECROSS MICROCATHETER COULD NOT BE ADVANCED. AFTER AN UNSPECIFIED BALLOON CATHETER WAS INSERTED AND DILATED UP TO ITS RATED BURST PRESSURE (RBP), THE FINECROSS MICROCATHETER WAS REPLACED BY AN ASAHI CORSAIR PRO XS MICROCATHETER. ADVANCED OVER THE SUOH 03 GUIDE WIRE AND WENT THROUGH A STENT STRUT, THE ASAHI CORSAIR PRO XS MICROCATHETER WAS TRAPPED, AND APPROXIMATELY A THIRD OF THE TIP SEGMENT OF THE MICROCATHETER WAS LEFT IN THE PATIENT ANATOMY. A NEW ASAHI CORSAIR PRO XS MICROCATHETER WAS USED TO APPROACH FROM A DIFFERENT SEPTAL BRANCH WITH SUCCESS. AN UNSPECIFIED STENT WAS DEPLOYED IN THE TARGET LESION, AND THE PROCEDURE WAS COMPLETED. IT WAS INFORMED THAT THERE WERE NO ADVERSE PATIENT EFFECTS CAUSED BY THE EVENT.

  Patient problems: Foreign Body In Patient

  MAUDE report 21146910 ↗
• InjurySep 26, 2022Difficult to Remove; Material Split, Cut or Torn; Difficult to Remove; Material Split, Cut or Torn

  IT WAS REPORTED THAT A PERCUTANEOUS CORONARY INTERVENTION (PCI) WAS PERFORMED TO TREAT A MODERATELY TORTUOUS, HEAVILY CALCIFIED CHRONIC TOTAL OCCLUSION (CTO) IN SEGMENTS #2-3 OF THE RIGHT CORONARY ARTERY (RCA). AN ASAHI ULTIMATE BROS 3 GUIDE WIRE AND AN ASAHI CORSAIR PRO XS MICROCATHETER WERE USED FOR A RETROGRADE APPROACH VIA SEPTAL COLLATERAL. WHEN ADVANCING THE TWO DEVICES TO THE LESION IN SEGMENT #2, THE CORSAIR PRO XS BECAME STUCK IN THE LESION. ALTHOUGH THE ULTIMATE BROS 3 WAS ABLE TO BE REMOVED, DIFFICULTY WAS MET WHEN REMOVING THE CORSAIR PRO XS. AN ASAHI RG3 GUIDE WIRE WAS THEN ADVANCED RETROGRADELY FOR EXTERNALIZATION. WHEN ATTEMPTING TO REMOVE THE CORSAIR PRO XS, THE TRAPPED CORSAIR PRO XS WAS NOT RELEASED EVEN THOUGH THE CATHETER SHAFT BECAME ELONGATED. AN UNSPECIFIED GUIDE WIRE WAS THEN ADVANCED ANTEGRADELY CLOSE TO THE TIP OF THE CORSAIR PRO XS. A BALLOON CATHETER WAS ADVANCED AND INFLATED TO RELEASE THE TRAPPED CORSAIR PRO XS. AFTER REMOVING THE CORSAIR PRO XS, THE PROCEDURE WAS RESUMED AND SUCCESSFULLY COMPLETED WITH REESTABLISHED BLOOD FLOW ACHIEVED BY STENTING. THERE WERE NO ADVERSE PATIENT EFFECTS RELATED TO THIS EVENT AND THE PATIENT WAS FINE WITHOUT COMPLICATIO

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15483339 ↗
• InjurySep 11, 2022Difficult to Remove; Detachment of Device or Device Component; Difficult to Remove; Detachment of Device or Device Component

  IT WAS REPORTED THAT AN ASAHI CORSAIR PRO XS MICROCATHETER AND AN ASAHI FIELDER XT-R GUIDE WIRE BECAME STUCK TO EACH OTHER DURING A PERCUTANEOUS CORONARY INTERVENTION (PCI) TO TREAT A CHRONIC TOTAL OCCLUSION (CTO) IN AN UNSPECIFIED SEGMENT OF THE CORONARY ARTERY. THE TWO DEVICES COULD NOT BE MANIPULATED AS INTENDED AND DIFFICULTY WAS MET IN REMOVAL. THE CONNECTOR OF THE CORSAIR PRO XS WAS CUT OFF AND AN UNSPECIFIED GUIDE EXTENSION CATHETER WAS USED TO REMOVE THE TWO DEVICES. THE PROCEDURE WAS THEN RESUMED AND SUCCESSFULLY COMPLETED WITH STENT DEPLOYMENT. THERE WERE NO ADVERSE PATIENT EFFECTS ASSOCIATED WITH THIS EVENT. CORSAIR PRO XS: MFR REPORT. FIELDER XT-R: MFR REPORT # 3003775027-2022-00106.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15398098 ↗
• InjuryMay 31, 2022Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT THE PATIENT HAD A NEAR COMPLETE CHRONIC TOTAL OCCLUSION (CTO) OF THE RIGHT CORONARY ARTERY (RCA) EXTENDING FROM MID-PROXIMAL RCA TO THE BIFURCATION OF THE POSTER DESCENDING BRANCH (PDA) AND POSTEROLATERAL BRANCH (PL). PRIOR STENT WAS PLACED AT THE VERY DISTAL SEGMENT OF THE RCA TO THE BIFURCATION. SUBINTIMAL TRACKING WITH RE-ENTRY WAS PLANNED IN STENT STRUT SEGMENT. IT WAS DIFFICULT TO ADVANCE AN UNSPECIFIED MICROCATHETER OVER AN ASAHI GUIDE WIRE. PHYSICIAN THEN SWITCHED OUT TO NON-ASAHI GUIDE WIRE. THE GUIDE WIRE WAS ABLE TO ADVANCE. THE CORSAIR PRO XS MICROCATHETER WAS ADVANCED FOLLOWING THE GUIDE WIRE, BASKET WEAVING IN AND OUT OF THE STENT STRUTS. THERE WAS A POINT WHERE THE CORSAIR PRO XS WAS TORQUED AND IT POPPED THROUGH, SIMILAR TO A MICROCATHER CROSSING A CALCIFIED CAP. THIS WAS MORE THAN LIKELY WHEN THE TIP RUBBED AGAINST THE EXISTING STENT STRUT. AFTER THE INITIAL PROCESS, THE GUIDE WIRE MARRIED TO THE CORSAIR PRO XS. ADVANCEMENT INTO THE PL OR PDA WAS TERMINATED AND BOTH PIECES OF EQUIPMENT WERE REMOVED. PHYSICIAN NOTED THE TIP OF THE CORSAIR PRO XS LOOKED SHREDDED. IT WAS NOTED THAT A PIECE OF THE TIP HAD BEEN LEFT IN THE SUBINTIMAL SPACE. NO ATTEMP

  Patient problems: Device Embedded In Tissue or Plaque

  MAUDE report 14545912 ↗
• InjuryMay 26, 2022Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT THE TIP OF AN ASAHI CORSAIR PRO XS MICROCATHETER HAD DISLODGED DURING A PERCUTANEOUS CORONARY INTERVENTION (PCI) TO TREAT A SEVERELY CALCIFIED CHRONIC TOTAL OCCLUSION (CTO) IN THE MID RIGHT CORONARY ARTERY (RCA). AFTER WIRING THE LESION, MULTIPLE NON-ASAHI MICROCATHETER AND 1.0 OR 1.5 BALLOONS WERE USED BUT THOSE WERE UNABLE TO CROSS. THE CORSAIR PRO XS WAS THEN ADVANCED BY TORQUING INTO THE LESION; HOWEVER, THE TIP BROKE OFF DUE TO THE VERY COMPLICATED CTO. BALLOON-ASSISTED SUBINTIMAL ENTRY (BASE) WAS PERFORMED PROXIMAL TO THE LESION TO COMPLETE THE CASE. THE SEPARATED TIP WAS DEEPLY BURIED IN THE LESION AND THEREFORE LEFT IN SITU. AS A STENT DEPLOY AT THE LESION COVERED THE SEPARATED TIP, THERE WERE NO CIRCULATION PROBLEMS. THERE WAS NO ADVERSE EFFECT ON THE PATIENT ASSOCIATED WITH THIS EVENT.

  Patient problems: Device Embedded In Tissue or Plaque

  MAUDE report 14519721 ↗
• MalfunctionMay 19, 2022Material Split, Cut or Torn

  PT HAD A NEAR COMPLETE CTO OF THE RCA EXTENDING FROM MID-PROX RCA TO THE BIFURCATION OF THE PDA/PL. PRIOR STENT PLACED AT THE VERY DISTAL SEGMENT OF THE RCA TO THE BIFURCATION. POSSIBLE SUBINTIMAL TRACKING WITH RE-ENTRY PRIOR TO DISTAL STENT. PHYSICIAN BELIEF THAT SUBINTIMAL RE-ENTRY IN STENT STRUT SEGMENT. DIFFICULTY ADVANCING MC OVER MONGO. PHYSICAIN SWITCHED OUT TO PILOT 200, WIRE WAS ABLE TO ADVANCE. WIRE MARRIED TO THE MC AT THIS TIME. XS AND PILOT 200 REMOVED, PHYSICIAN NOTED THE TIP LOOK SHREDDED. PER DR. KOURANY, "A SLIVER OF THE TIP WAS LEFT IN THE SUBINTIMAL SPACE. I BELIEVE THE TIP WAS DEFORMED PASSING THROUGH THE EXISTING STENT STRUTS."

  Patient problems: Foreign Body In Patient

  MAUDE report 14438434 ↗
• MalfunctionMay 12, 2022Entrapment of Device

  TIP WAS DISLODGED IN LESION.

  Patient problems: Foreign Body In Patient

  MAUDE report 14367144 ↗
• InjuryJul 7, 2021Material Twisted/Bent; Material Twisted/Bent

  IT WAS REPORTED THAT A PERCUTANEOUS CORONARY INTERVENTION (PCI) WAS PERFORMED TO TREAT A HEAVILY CALCIFIED CHRONIC TOTAL OCCLUSION (CTO) LESION IN THE PROXIMAL-MID LEFT ANTERIOR DESCENDING ARTERY (LAD). AN ASAHI CORSAIR PRO XS MICROCATHETER WAS USED FOR A RETROGRADE APPROACH FROM THE RIGHT CORONARY ARTERY (RCA) VIA A SEPTAL COLLATERAL AND PASSED THROUGH THE COLLATERAL CHANNEL WITHOUT PROBLEM. WHEN ADVANCING THE CORSAIR PRO XS ALONG WITH AN ASAHI ULTIMATEBROS 3 GUIDE WIRE, ANGIO IMAGES REVEALED THAT THE TIP OF THE CORSAIR PRO XS WAS DEFORMED. WHEN ATTEMPTS WERE MADE TO REMOVE THE CORSAIR PRO XS, IT WAS NOTED THAT THE MICROCATHETER WAS STUCK TO THE ULTIMATE BROS 3 AND THEREFORE BOTH OF THE DEVICES WERE REMOVED AS A UNIT. THE DEVICE WAS REPLACED TO RESUME THE PROCEDURE. THE PCI WAS SUCCESSFULLY COMPLETED WITH STENT DEPLOYMENT. THERE WERE NO ADVERSE PATIENT EFFECTS ASSOCIATED WITH THIS EVENT. THE PATIENT WAS REPORTEDLY FINE WITHOUT PROBLEM AFTER THE PROCEDURE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12132726 ↗
• MalfunctionFeb 28, 2021Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT THE TIP OF AN ASAHI CORSAIR PRO XS MICROCATHETER DETACHED DURING A PERCUTANEOUS CORONARY INTERVENTION (PCI) TO TREAT A HEAVILY CALCIFIED 90-95% STENOSIS IN THE MID LEFT CIRCUMFLEX ARTERY (LCX). THE PHYSICIAN USED A NON-ASAHI RUNTHROUGH WIRE TO CROSS THE MID LCX HEAVILY CALCIFIED LESION. FIRST HE USED A NON-ASAHI TURNPIKE SPIRAL MICROCATHETER BUT IT WAS UNABLE TO ADVANCE ACROSS LESION. HE THEN TRIED CORSAIR PRO XS. HE WAS UNABLE TO ADVANCE ACROSS THE LESION. WHEN HE TRIED TO REMOVE THE CORSAIR PRO XS, HE NOTICED THE MICROCATHETER WOULD NOT COME OFF WIRE. HE PULLED THE MICROCATHETER AND WIRE OUT OF THE GUIDE. HE NOTICED THE TIP WAS SEPARATED FROM THE SHAFT AND WAS STUCK ON THE WIRE. HE USED ANOTHER RUNTHROUGH WIRE TO CROSS THE LESION. THEN HE USED A NON-ASAHI MAMBA FLEX MICROCATHETER AND TRIED TO CROSS THE LESION BUT IT WOULD NOT CROSS THE LESION. THE PATIENT WAS FINE, NO ADVERSE OUTCOMES ASSOCIATED WITH THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11391022 ↗
• MalfunctionFeb 19, 2021Material Separation; Failure to Advance; Mechanical Jam

  PER SCRUB TECH-DR. BISEN USED A TERUMO RUNTHROUGH WIRE TO CROSS MID CX HEAVILY CALCIFIED LESION. FIRST HE USED A TURNPIKE SPIRAL MICROCATHETER BUT IT WAS UNABLE TO ADVANCE ACROSS LESION. HE THEN TRIED CORSAIR PRO XS. HE WAS UNABLE TO ADVANCE ACROSS THE LESION. WHEN HE TRIED TO REMOVE THE CORSAIR PRO XS, HE NOTICED THE MICROCATHETER WOULD NOT COME OFF WIRE. HE PULLED MC AND WIRE OUT OF THE GUIDE. HE NOTICED THE TIP WAS SEPARATED FROM THE SHAFT AND WAS STUCK ON THE WIRE. HE USED ANOTHER RUNTHROUGH WIRE TO CROSS THE LESION. THEN HE USED A MAMBA FLEX MICROCATHETER AND TRIED TO CROSS THE LESION BUT IT WOULDN'T CROSS THE LESION. HE REMOVED THE MAMBA AND WIRE BECAUSE HE NOTICED THAT THE TIP HAD ALSO SEPARATED FROM THE MAMBA MC. PATIENT WAS FINE, NO ADVERSE OUTCOMES.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11350032 ↗
• InjuryFeb 9, 2021Material Fragmentation; Difficult to Remove; Material Twisted/Bent; Material Fragmentation; Difficult to Remove; Material Twisted/Bent

  IT WAS REPORTED THAT AN ASAHI CORSAIR PRO XS MICROCATHETER BECAME STUCK ON A CONCOMITANT GUIDE WIRE DURING A RETROGRADE PCI TO TREAT A CTO IN THE DISTAL RCA. THE MICROCATHETER WAS DELIVERED TO THE RCA VIA THE SVG WHEN THE CORSAIR PRO XS GOT STUCK IN A PREVIOUSLY PLACED STENT IN THE SVG. WHEN TRYING TO REMOVE THE MICROCATHETER, IT BECAME TRAPPED ON THE WIRE. DURING ATTEMPTS TO REMOVE THE MICROCATHETER, THE HUB PULLED OFF THE MICROCATHETER SHAFT. SUBSEQUENTLY THE MICROCATHETER AND THE OLD STENTS HAD TO BE SNARED. THE PCI WAS SUCCESSFULLY COMPLETED. THERE WERE NO ADVERSE PATIENT EFFECTS ASSOCIATED WITH THIS EVENT. THE PHYSICIAN COMMENTED THAT HE DID NOT THINK THE MICROCATHETER GETTING STUCK WAS A FAILURE OF THE MICROCATHETER. THE WIRE MUST HAVE GOTTEN BEHIND THE STENT AND THAT WAS WHY THE MICROCATHETER GOT TRAPPED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11299353 ↗
• MalfunctionJan 27, 2021Entrapment of Device; Physical Resistance/Sticking

  WHILE USING THE SVG TO RCA AS A RETROGRADE APPROACH, THE CORSAIR PRO XS GOT STUCK IN A PREVIOUSLY PLACED STENT IN THE SVG. WHEN TRYING TO REMOVE THE MC, THE CATHETER BECAME TRAPPED ON THE WIRE. AS DR. NEUPANE TRIED TO PULL THE MC BACK, THE HUB PULLED OFF THE MC AND HE SUBSEQUENTLY HAD TO SNARE THE MC AND OLD STENTS OUT.

  Patient problems: Insufficient Information

  MAUDE report 11237972 ↗

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