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TPLC
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show TPLC since
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2024
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Device
aid, surgical, viscoelastic
Product Code
LZP
Regulation Number
886.4275
Device Class
3
Premarket Approvals (PMA)
2016
2017
2018
2019
2020
2021
2022
2023
2024
12
18
8
5
13
15
8
13
4
MDR Year
MDR Reports
MDR Events
2016
136
136
2017
162
162
2018
113
113
2019
156
156
2020
132
132
2021
157
157
2022
184
184
2023
107
107
2024
21
21
Device Problems
MDRs with this Device Problem
Events in those MDRs
Adverse Event Without Identified Device or Use Problem
590
590
Contamination
124
124
Device Contamination with Chemical or Other Material
107
107
Insufficient Information
72
72
Appropriate Term/Code Not Available
47
47
Detachment of Device or Device Component
26
26
Device Contaminated During Manufacture or Shipping
22
22
Difficult to Remove
18
18
Leak/Splash
17
17
Disconnection
16
16
Particulates
15
15
Mechanical Problem
14
14
Delivered as Unsterile Product
12
12
Contamination /Decontamination Problem
12
12
Patient-Device Incompatibility
11
11
Manufacturing, Packaging or Shipping Problem
11
11
Device Operates Differently Than Expected
10
10
Detachment Of Device Component
7
7
Separation Problem
7
7
Break
7
7
Product Quality Problem
5
5
Device Handling Problem
5
5
Positioning Problem
5
5
Device Markings/Labelling Problem
5
5
Material Integrity Problem
3
3
Use of Device Problem
3
3
Obstruction of Flow
3
3
Failure to Align
2
2
Split
2
2
Microbial Contamination of Device
2
2
Improper or Incorrect Procedure or Method
2
2
Material Separation
2
2
Burst Container or Vessel
2
2
Complete Blockage
2
2
Material Fragmentation
2
2
Material Opacification
2
2
Physical Resistance/Sticking
2
2
Operating System Becomes Nonfunctional
2
2
Connection Problem
2
2
Contamination of Device Ingredient or Reagent
2
2
Material Deformation
2
2
Lack of Maintenance Documentation or Guidelines
1
1
Device Packaging Compromised
1
1
Device Dislodged or Dislocated
1
1
Human-Device Interface Problem
1
1
Chemical Problem
1
1
Device Contamination With Biological Material
1
1
Optical Problem
1
1
Packaging Problem
1
1
Scratched Material
1
1
Torn Material
1
1
No Apparent Adverse Event
1
1
Sharp Edges
1
1
Device Contaminated at the User Facility
1
1
Overheating of Device
1
1
Unsealed Device Packaging
1
1
Labelling, Instructions for Use or Training Problem
1
1
Occlusion Within Device
1
1
Device Emits Odor
1
1
Coagulation in Device or Device Ingredient
1
1
Unintended Ejection
1
1
Fluid/Blood Leak
1
1
Crack
1
1
Degraded
1
1
Shelf Life Exceeded
1
1
Defective Component
1
1
Therapy Delivered to Incorrect Body Area
1
1
Loss of Power
1
1
Precipitate in Device or Device Ingredient
1
1
Component Missing
1
1
Fungus in Device Environment
1
1
Tear, Rip or Hole in Device Packaging
1
1
Structural Problem
1
1
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
Intraocular Pressure Increased
210
210
No Clinical Signs, Symptoms or Conditions
142
142
No Consequences Or Impact To Patient
135
135
Inflammation
115
115
Toxic Anterior Segment Syndrome (TASS)
101
101
No Code Available
97
97
Corneal Edema
97
97
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available
90
90
Endophthalmitis
88
88
No Known Impact Or Consequence To Patient
72
72
Uveitis
53
53
Blurred Vision
46
46
Capsular Bag Tear
40
40
Pain
37
37
Visual Impairment
33
33
Eye Burn
30
30
Toxicity
30
30
Eye Injury
26
26
Hyphema
24
24
Hypopyon
21
21
Vitrectomy
20
20
Loss of Vision
19
19
Foreign Body In Patient
19
19
No Information
17
17
Eye Pain
17
17
Conjunctivitis
15
15
Unspecified Infection
14
14
No Patient Involvement
14
14
Clouding, Central Corneal
12
12
Hemorrhage/Bleeding
11
11
Iritis
9
9
Intraocular Pressure Decreased
9
9
Vitritis
8
8
Vitreous Loss
8
8
Red Eye(s)
7
7
Corneal Decompensation
7
7
Headache
7
7
Macular Edema
7
7
Fibrosis
7
7
Irritation
6
6
Nausea
6
6
Visual Disturbances
6
6
Reaction
6
6
Rupture
5
5
Vitreous Floaters
5
5
Bacterial Infection
4
4
Injury
4
4
Burn, Thermal
4
4
Keratitis
4
4
Device Embedded In Tissue or Plaque
4
4
Eye Infections
4
4
Complaint, Ill-Defined
3
3
Zonular Dehiscence
3
3
Retinal Detachment
3
3
Vitreous Hemorrhage
3
3
Cataract
3
3
Intraocular Infection
3
3
Corneal Clouding/Hazing
3
3
Glaucoma
2
2
Hyperemia
2
2
Intraocular Pressure, Delayed, Uncontrolled
2
2
Corneal Abrasion
2
2
Corneal Stromal Edema
2
2
Edema
2
2
Vomiting
2
2
Itching Sensation
2
2
Perforation
2
2
Discomfort
2
2
Patient Problem/Medical Problem
2
2
Swelling/ Edema
2
2
Insufficient Information
1
1
Respiratory Insufficiency
1
1
Excessive Tear Production
1
1
Anxiety
1
1
Discharge
1
1
Blood Loss
1
1
Skin Inflammation
1
1
Occlusion
1
1
Scarring
1
1
Swelling
1
1
Toxic Shock Syndrome
1
1
Burning Sensation
1
1
Foreign Body Sensation in Eye
1
1
Erythema
1
1
Infarction, Cerebral
1
1
Burn(s)
1
1
Capsular Contracture
1
1
Adhesion(s)
1
1
Autoimmune Reaction
1
1
Ischemia
1
1
Hypersensitivity/Allergic reaction
1
1
High Blood Pressure/ Hypertension
1
1
Recalls
Manufacturer
Recall Class
Date Posted
1
Abbott Medical Optics Inc. (AMO)
II
May-10-2017
2
Johnson & Johnson Surgical Vision Inc
II
Jan-27-2020
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