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

TPLC - Total Product Life Cycle

  • 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
 

New Search show TPLC since Back to Search Results
Device endoscopic guidewire, gastroenterology-urology
Regulation Description Endoscope and accessories.
Definition To provide access to gi or gu tract for the purpose of passing or exchanging other accessories.
Product CodeOCY
Regulation Number 876.1500
Device Class 2

MDR Year MDR Reports MDR Events
2020 128 128
2021 94 94
2022 134 134
2023 115 115
2024 131 131
2025 25 25

Device Problems MDRs with this Device Problem Events in those MDRs
Peeled/Delaminated 294 294
Material Separation 87 87
Break 75 75
Adverse Event Without Identified Device or Use Problem 51 51
Detachment of Device or Device Component 25 25
Material Twisted/Bent 19 19
Material Fragmentation 19 19
Insufficient Information 13 13
Material Deformation 12 12
Unraveled Material 11 11
Deformation Due to Compressive Stress 10 10
Appropriate Term/Code Not Available 9 9
Fracture 9 9
Entrapment of Device 8 8
Difficult to Advance 8 8
Device Contaminated During Manufacture or Shipping 7 7
Positioning Failure 7 7
Device Damaged by Another Device 5 5
Positioning Problem 5 5
Device Damaged Prior to Use 5 5
Material Split, Cut or Torn 5 5
Difficult to Remove 4 4
Microbial Contamination of Device 4 4
Defective Device 4 4
Difficult to Insert 4 4
Unsealed Device Packaging 4 4
Use of Device Problem 4 4
Accessory Incompatible 3 3
Physical Resistance/Sticking 3 3
Improper or Incorrect Procedure or Method 3 3
Contamination /Decontamination Problem 2 2
Particulates 2 2
Inadequate Lubrication 2 2
Material Integrity Problem 1 1
Contamination 1 1
Scratched Material 1 1
Collapse 1 1
Crack 1 1
Difficult or Delayed Positioning 1 1
Product Quality Problem 1 1
Tear, Rip or Hole in Device Packaging 1 1
Material Protrusion/Extrusion 1 1
No Apparent Adverse Event 1 1
Migration 1 1
Device-Device Incompatibility 1 1
Device Slipped 1 1
Flaked 1 1
Loose or Intermittent Connection 1 1
Material Frayed 1 1
Mechanical Jam 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 388 388
No Consequences Or Impact To Patient 85 85
Foreign Body In Patient 65 65
Insufficient Information 24 24
Pancreatitis 14 14
Hemorrhage/Bleeding 13 13
Swelling/ Edema 12 12
Perforation 11 11
No Known Impact Or Consequence To Patient 10 10
No Code Available 7 7
No Patient Involvement 7 7
Pain 7 7
Device Embedded In Tissue or Plaque 6 6
Tingling 4 4
Laceration(s) of Esophagus 4 4
Peritonitis 4 4
Discomfort 4 4
Bacterial Infection 4 4
Perforation of Esophagus 3 3
Twitching 3 3
Sepsis 2 2
Gastrointestinal Hemorrhage 2 2
No Information 2 2
Inflammation 2 2
Laceration(s) 2 2
Abdominal Pain 1 1
Air Embolism 1 1
Unspecified Infection 1 1
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available 1 1
Death 1 1
Bowel Perforation 1 1
Abrasion 1 1
Fever 1 1
Retroperitoneal Hemorrhage 1 1
Septic Shock 1 1
Vomiting 1 1
Biliary Cirrhosis 1 1
Internal Organ Perforation 1 1
Respiratory Failure 1 1
Fistula 1 1

Recalls
Manufacturer Recall Class Date Posted
1 Cook Inc. II Feb-04-2020
2 Cook Incorporated II Sep-28-2022
-
-