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TPLC
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show TPLC since
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2024
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Device
bed, patient rotation, powered
Product Code
IKZ
Regulation Number
890.5225
Device Class
2
MDR Year
MDR Reports
MDR Events
2015
40
40
2016
26
26
2017
35
35
2018
28
28
2019
27
27
2020
29
29
2021
11
11
2022
6
6
2023
20
20
2024
5
5
Device Problems
MDRs with this Device Problem
Events in those MDRs
Adverse Event Without Identified Device or Use Problem
78
78
Insufficient Information
22
22
Difficult to Open or Close
17
17
Use of Device Problem
16
16
Break
11
11
Electrical /Electronic Property Problem
11
11
Device Handling Problem
9
9
Device Inoperable
8
8
Defective Component
8
8
Device Operates Differently Than Expected
7
7
Mechanical Problem
6
6
Patient Device Interaction Problem
6
6
Unintended Movement
5
5
Unintended System Motion
5
5
Detachment Of Device Component
4
4
Patient-Device Incompatibility
4
4
Positioning Problem
4
4
No Apparent Adverse Event
4
4
Human Factors Issue
4
4
No Display/Image
4
4
Device Displays Incorrect Message
4
4
Material Too Soft/Flexible
3
3
Difficult To Position
3
3
Detachment of Device or Device Component
3
3
Cut In Material
3
3
Device Slipped
3
3
Sharp Edges
3
3
Device Issue
3
3
Human-Device Interface Problem
2
2
Sticking
2
2
Product Quality Problem
2
2
Loose or Intermittent Connection
2
2
Mechanical Jam
2
2
Low Audible Alarm
2
2
Device Dislodged or Dislocated
2
2
Difficult or Delayed Positioning
2
2
Inflation Problem
2
2
Scratched Material
2
2
Deflation Problem
2
2
Defective Device
2
2
Material Integrity Problem
2
2
Device Alarm System
2
2
Device Difficult to Program or Calibrate
1
1
Misconnection
1
1
Application Interface Becomes Non-Functional Or Program Exits Abnormally
1
1
Unintended Ejection
1
1
Failure to Power Up
1
1
Material Too Rigid or Stiff
1
1
Appropriate Term/Code Not Available
1
1
Physical Resistance/Sticking
1
1
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
Pressure Sores
65
65
No Consequences Or Impact To Patient
37
37
No Known Impact Or Consequence To Patient
29
29
Injury
20
20
No Clinical Signs, Symptoms or Conditions
12
12
Tissue Damage
12
12
Death
11
11
Pain
9
9
Fall
8
8
Low Oxygen Saturation
7
7
No Information
6
6
Tissue Breakdown
6
6
Insufficient Information
4
4
Cardiac Arrest
3
3
Skin Tears
3
3
Complaint, Ill-Defined
2
2
Hypoventilation
2
2
No Code Available
2
2
No Patient Involvement
2
2
Cardiopulmonary Arrest
2
2
Physical Entrapment
2
2
Tachycardia
2
2
Hyperemia
2
2
Patient Problem/Medical Problem
1
1
Electric Shock
1
1
Failure of Implant
1
1
Necrosis
1
1
Bone Fracture(s)
1
1
Skin Disorders
1
1
Contusion
1
1
Skin Discoloration
1
1
Foreign Body In Patient
1
1
Loss Of Pulse
1
1
Dyspnea
1
1
Laceration(s)
1
1
Scar Tissue
1
1
Bradycardia
1
1
Unspecified Tissue Injury
1
1
Extubate
1
1
Unintended Extubation
1
1
Recalls
Manufacturer
Recall Class
Date Posted
1
Arjo Hospital Equipment AB
II
Feb-27-2015
2
Arjohuntleigh Magog
II
Feb-05-2019
3
Kinsman Enterprises Inc
II
Oct-21-2021
4
Stryker Medical Division of Stryker Corporation
II
Aug-06-2021
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