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TPLC
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show TPLC since
2009
2010
2011
2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
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Device
acid, hyaluronic, intraarticular
Product Code
MOZ
Device Class
3
Premarket Approvals (PMA)
2009
2010
2011
2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
10
7
9
12
10
28
21
21
16
21
12
22
20
20
13
9
MDR Year
MDR Reports
MDR Events
2014
340
340
2015
293
293
2016
313
313
2017
506
506
2018
1096
1096
2019
567
567
2020
441
441
2021
375
375
2022
305
305
2023
471
471
2024
184
184
Device Problems
MDRs with this Device Problem
Events in those MDRs
Adverse Event Without Identified Device or Use Problem
2708
2708
Insufficient Information
552
552
Device Contamination With Biological Material
531
531
Patient-Device Incompatibility
425
425
Microbial Contamination of Device
176
176
Off-Label Use
118
118
Nonstandard Device
96
96
Device Operates Differently Than Expected
77
77
Appropriate Term/Code Not Available
75
75
Improper or Incorrect Procedure or Method
46
46
Break
38
38
Therapeutic or Diagnostic Output Failure
37
37
Use of Device Problem
36
36
No Apparent Adverse Event
29
29
Unexpected Therapeutic Results
24
24
Patient Device Interaction Problem
22
22
Leak/Splash
11
11
Manufacturing, Packaging or Shipping Problem
10
10
Lack of Effect
9
9
Contamination
7
7
Detachment of Device or Device Component
7
7
Product Quality Problem
6
6
Device Markings/Labelling Problem
6
6
Defective Device
5
5
Fluid/Blood Leak
5
5
Contamination of Device Ingredient or Reagent
5
5
Loss of Data
4
4
Application Program Problem: Medication Error
4
4
Output Problem
3
3
Failure to Deliver
3
3
Device Fell
3
3
Material Separation
3
3
Missing Value Reason
3
3
Device Appears to Trigger Rejection
2
2
Inaccurate Delivery
2
2
Device Dislodged or Dislocated
2
2
Fracture
2
2
Device Contamination with Chemical or Other Material
2
2
Device Handling Problem
2
2
Improper Flow or Infusion
2
2
Difficult to Insert
2
2
Expiration Date Error
2
2
Contamination /Decontamination Problem
2
2
Patient Data Problem
2
2
Defective Component
2
2
Unstable
2
2
Device Inoperable
2
2
Therapy Delivered to Incorrect Body Area
1
1
Device Damaged Prior to Use
1
1
Noise, Audible
1
1
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
Pain
1323
1323
Arthralgia
994
994
No Code Available
991
991
Joint Swelling
794
794
Swelling
695
695
Ambulation Difficulties
500
500
Joint Disorder
383
383
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available
312
312
Arthritis
292
292
Inflammation
236
236
Hypersensitivity/Allergic reaction
229
229
Unspecified Infection
214
214
Swelling/ Edema
207
207
Insufficient Information
205
205
Reaction
171
171
Erythema
167
167
Reaction, Injection Site
165
165
Bacterial Infection
140
140
Synovitis
127
127
Fever
127
127
Loss of Range of Motion
123
123
Rash
118
118
No Known Impact Or Consequence To Patient
113
113
Death
109
109
Nausea
97
98
No Clinical Signs, Symptoms or Conditions
96
96
Headache
94
94
Discomfort
79
79
Fatigue
77
77
Dyspnea
77
77
Itching Sensation
76
76
Edema
71
71
Therapeutic Response, Decreased
71
71
Chills
69
69
Sleep Dysfunction
62
62
Dizziness
61
61
Fall
60
60
Inadequate Pain Relief
60
60
Fluid Discharge
57
57
Burning Sensation
54
54
Muscle Weakness
46
46
Toxicity
45
45
High Blood Pressure/ Hypertension
41
41
Weakness
40
40
Myalgia
40
40
Peripheral Edema
40
40
Vomiting
39
39
Numbness
39
39
Disability
36
36
Malaise
35
35
Recalls
Manufacturer
Recall Class
Date Posted
1
Ferring Pharmaceuticals Inc
III
May-21-2010
2
Sanofi Genzyme
II
Feb-14-2018
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