• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: WILSON-COOK MEDICAL INC MEMORY HARD WIRE BASKET; FFL, DISLODGER, STONE, BASKET, URETHRAL, METAL

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

WILSON-COOK MEDICAL INC MEMORY HARD WIRE BASKET; FFL, DISLODGER, STONE, BASKET, URETHRAL, METAL Back to Search Results
Catalog Number MWB-3X6
Device Problem Adverse Event Without Identified Device or Use Problem (2993)
Patient Problems Gastrointestinal Hemorrhage (4476); Pancreatitis (4481)
Event Type  Injury  
Event Description
Cook became aware of the clinical literature article involving cook memory hard wire baskets."from january 2013 to january 2019, a total of 1555 consecutive patients diagnosed with cholecystolithiasis combined with choledocholithiasis who underwent surgical treatment in tongji hospital were retrospectively analyzed." "[ercp group]following deep cannulation, retrograde cholangiography, sphincterotomy or balloon expansion (wilson-cook tx-15-a), the cbd stones were extracted by a basket (wilson-cook mwb-3x6) until no stones were confirmed by repeat cholangiogram.Mechanical lithotripsy was used to retrieve the stones if needed." "there were more postoperative complications in ercp + lc group (3.6%)"."five patients (4 in ercp + lc group and 1 in tri-scope group) with pancreatitis recovered with conservative treatment.Three cases appeared with hemorrhage in ercp + lc group, of which two patients were well-healed with hemostatic and fluid therapy, and one patient was cured with interventional therapy.Totally 8 patients (0.8%) developed bile leakage and recovery after drainage within 1¿3 days during hospitalization." "no patient converted to open surgery in three groups." postoperative complications: outcomes of patients with cholecystolithiasis combined with choledocholithiasis ercp+lc (n= 275), pancreatitis (%) 4 (1.5), bile leak (%) 0 (0.0), bleeding (%) 3 (1.1), cholangitis (%) 3 (1.1).Outcomes of ercp + lc group and tri-scope group: ercp + lc (n= 275) tri-scope (n = 479) p postop complications 10 (3.6) pancreatitis (%) 4 (1.5) 1 (0.2) 0.118 bile leak (%) 0 (0.0) 5 (1.0) 0.174 bleeding (%) 3 (1.1) 3 (0.6) 0.791 cholangitis (%) 3 (1.1).Outcomes of ercp + lc group and ltcbde group: ercp + lc(n = 275) ltcbde(n = 280) p postop complications 10 (3.6) 3 (1.1) ¿ pancreatitis (%) 4 (1.5) 0 (0.0) 0.128 bile leak (%) 0 (0.0) 3 (1.1) 0.257 bleeding (%) 3 (1.1) 0 (0.0) 0.241 cholangitis (%) 3 (1.1).Intervention was required as noted in the article but as also noted in the article, "no patient converted to open surgery in three groups." the subject of this report are the four (4) events of pancreatitis, three (3) events of bleeding, and three (3) events of cholangitis.
 
Manufacturer Narrative
Investigation evaluation: a product evaluation was not performed in response to this report because the product said to be involved was not provided to cook for evaluation.The report could not be confirmed.A review of the device history record could not be conducted because the lot number was not provided.Investigation conclusion: we could not conduct a complete investigation because the product said to be involved was not returned for evaluation.A definitive cause for the reported observation could not be determined.However, a device failure was not reported, only post procedure complications.Pancreatitis, cholangitis, and bleeding are known complications of gastrointestinal endoscopy and ercp.The ifu lists potential complications: "those associated with gastrointestinal endoscopy and ercp include, but are not limited to: pancreatitis, cholangitis, sepsis, perforation, hemorrhage, aspiration, fever, infection, hypotension, allergic reaction, respiratory depression or arrest, cardiac arrhythmia or arrest." prior to distribution, all memory hard wire baskets are subjected to a visual inspection and functional testing to ensure device integrity.Corrective action: a review of the complaint history was conducted.The likelihood of occurrence is considered rare.Corrective action is not warranted at this time based on the quality engineering risk assessment.Quality assurance will continue to monitor for complaint trends and reassess the risk assessment results as post market feedback continues to become available.Guo t, wang l, xie p, zhang z, huang x, yu y.Surgical methods of treatment for cholecystolithiasis combined with choledocholithiasis: six years' experience of a single institution.Surg endosc.2022 jul;36(7):4903-4911.Doi: 10.1007/s00464-021-08843-x.Epub 2021 nov 3.Pmid: 34731303; pmcid: pmc9160127.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
MEMORY HARD WIRE BASKET
Type of Device
FFL, DISLODGER, STONE, BASKET, URETHRAL, METAL
Manufacturer (Section D)
WILSON-COOK MEDICAL INC
4900 bethania station rd
winston-salem NC 27105
Manufacturer (Section G)
COOK ENDOSCOPY
4900 bethania station rd
winston-salem NC 27105
Manufacturer Contact
sabrina o'brien
4900 bethania station rd
winston-salem, NC 27105
3367440157
MDR Report Key17661585
MDR Text Key322394492
Report Number1037905-2023-00410
Device Sequence Number1
Product Code FFL
Combination Product (y/n)N
Reporter Country CodeCH
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Foreign,Literature
Reporter Occupation Physician
Type of Report Initial
Report Date 08/31/2023
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received08/31/2023
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Health Professional
Device Catalogue NumberMWB-3X6
Device Lot NumberUNKNOWN
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Date Manufacturer Received08/11/2023
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Is the Device Single Use? No
Type of Device Usage Initial
Patient Sequence Number1
Treatment
SCOPE, UNKNOWN MAKE AND MODEL
Patient Outcome(s) Required Intervention;
-
-