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TPLC
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show TPLC since
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Device
gram negative identification panel
Product Code
LQM
Regulation Number
866.2660
Device Class
1
MDR Year
MDR Reports
MDR Events
2015
69
69
2016
1
1
2017
77
77
2018
88
88
2019
12
12
2021
3
3
2022
7
7
2023
30
30
2024
31
31
Device Problems
MDRs with this Device Problem
Events in those MDRs
Incorrect Or Inadequate Test Results
161
161
Incorrect, Inadequate or Imprecise Result or Readings
137
137
Device Operates Differently Than Expected
7
7
Difficult to Open or Remove Packaging Material
6
6
Appropriate Term/Code Not Available
2
2
False Positive Result
2
2
False Negative Result
1
1
Adverse Event Without Identified Device or Use Problem
1
1
Device Emits Odor
1
1
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
No Known Impact Or Consequence To Patient
92
92
No Patient Involvement
92
92
No Clinical Signs, Symptoms or Conditions
71
71
No Consequences Or Impact To Patient
45
45
Injury
6
6
Misdiagnosis
4
4
No Information
4
4
Not Applicable
2
2
Pain
2
2
Vomiting
1
1
Bacterial Infection
1
1
Recalls
Manufacturer
Recall Class
Date Posted
1
Biomerieux Inc
II
Jan-04-2023
2
Biomerieux Inc
II
May-22-2017
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