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TPLC
New Search
show TPLC since
2009
2010
2011
2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
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Device
barrier, absorbable, adhesion
Product Code
MCN
Device Class
3
Premarket Approvals (PMA)
2009
2010
2011
2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
2
5
8
4
3
1
2
7
5
1
7
7
8
7
4
7
MDR Year
MDR Reports
MDR Events
2014
53
53
2015
68
68
2016
71
71
2017
58
58
2018
65
65
2019
55
55
2020
44
44
2021
42
42
2022
53
53
2023
45
45
2024
17
17
Device Problems
MDRs with this Device Problem
Events in those MDRs
Adverse Event Without Identified Device or Use Problem
314
314
Appropriate Term/Code Not Available
89
89
Other (for use when an appropriate device code cannot be identified)
29
29
Migration or Expulsion of Device
27
27
Insufficient Information
27
27
Material Erosion
17
17
Patient-Device Incompatibility
17
17
Defective Device
8
8
Device Operates Differently Than Expected
7
7
Improper or Incorrect Procedure or Method
6
6
Unsealed Device Packaging
5
5
Unexpected Therapeutic Results
4
4
Delivered as Unsterile Product
3
3
Device Contaminated During Manufacture or Shipping
3
3
Microbial Contamination of Device
3
3
Device Markings/Labelling Problem
3
3
Failure To Adhere Or Bond
2
2
Device Contamination with Chemical or Other Material
2
2
Tear, Rip or Hole in Device Packaging
2
2
Therapeutic or Diagnostic Output Failure
2
2
Nonstandard Device
2
2
Material Deformation
1
1
Material Rupture
1
1
Packaging Problem
1
1
Use of Device Problem
1
1
Positioning Failure
1
1
Obstruction of Flow
1
1
Detachment Of Device Component
1
1
Loss of or Failure to Bond
1
1
Device Issue
1
1
Manufacturing, Packaging or Shipping Problem
1
1
Reaction
1
1
Material Disintegration
1
1
Physical Property Issue
1
1
Physical Resistance/Sticking
1
1
Malposition of Device
1
1
Incomplete or Missing Packaging
1
1
Entrapment of Device
1
1
Product Quality Problem
1
1
Device Misassembled During Manufacturing /Shipping
1
1
Contamination
1
1
Contamination /Decontamination Problem
1
1
Leak/Splash
1
1
Extrusion
1
1
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
No Code Available
135
135
Pain
129
129
Unspecified Infection
121
121
Abscess
112
112
Adhesion(s)
100
100
Fever
72
72
Inflammation
54
54
Obstruction/Occlusion
51
51
Peritonitis
48
48
Erosion
45
45
Not Applicable
41
41
Surgical procedure
26
26
Abdominal Pain
25
25
Hypersensitivity/Allergic reaction
16
16
Wound Dehiscence
15
15
Vomiting
15
15
Scar Tissue
14
14
No Consequences Or Impact To Patient
13
13
Other (for use when an appropriate patient code cannot be identified)
13
13
Injury
13
13
Fistula
12
12
Treatment with medication(s)
12
12
Bacterial Infection
12
12
Blood Loss
11
11
Fluid Discharge
10
10
No Clinical Signs, Symptoms or Conditions
10
10
Incontinence
9
9
Foreign Body Reaction
9
9
Edema
9
9
Insufficient Information
8
8
Purulent Discharge
8
8
Discharge
8
8
Reaction
7
7
Post Operative Wound Infection
7
7
Ascites
7
7
Hemorrhage/Bleeding
7
7
Diarrhea
7
7
Nausea
6
6
Abdominal Distention
6
6
Headache
6
6
Organ Dehiscence
6
6
Paralysis
5
5
Rash
5
5
Foreign Body In Patient
5
5
Erythema
5
5
Swelling
5
5
Unspecified Tissue Injury
5
5
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available
4
4
Discomfort
4
4
Impaired Healing
4
4
Recalls
Manufacturer
Recall Class
Date Posted
1
Baxter Healthcare Corporation
II
Apr-25-2024
2
Genzyme Corporation
II
Jun-21-2012
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