C-PICK, PLASTIC CLAMPS

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2013-03-01 for C-PICK, PLASTIC CLAMPS manufactured by .

Event Text Entries

[3296502] In (b)(6) 1982, i had a vasectomy at (b)(6) in (b)(6) by (b)(6). After having this done my groin and testicle area, mainly on my left side. "to dr about it at several other visits and received no real explanation for the pain i was having". If i bumped that area very lightly it would cause severe pain. I think the plastic clamps that were used on the area are the blame. The pain continued to persist and increased slowly so that by (b)(6), i was having trouble bending forward even slightly. Enough so that i was being forced to kneel down to do what i was going to do instead of bending. The pain seems to move, other side lower back and it is getting worse almost daily. Despite many x-rays, mri, cat scans at (b)(6) both (b)(6)s and more. None has found a reason or cure. I believe the clamps used did not dissolve as the doctor said they would, or something with the sutures to close the incisions are the problem. In the last 6 months or so it seems to even make a difference with different types of upper and lower body movement. Your attention to this problem would be appreciated, because i have exhausted all other attempts to get the help i need to solve this matter. Thank you.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5029313
MDR Report Key3001669
Date Received2013-03-01
Date of Report2013-03-13
Date of Event1982-03-01
Date Added to Maude2013-03-14
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Reporter OccupationPATIENT
Health Professional0
Initial Report to FDA3
Report to FDA0
Event Location0
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameC-PICK, PLASTIC CLAMPS
Generic NameUNK
Product CodeNJC
Date Received2013-03-01
Device Sequence No1
Device Event Key0


Patients

Patient NumberTreatmentOutcomeDate
10 2013-03-01

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