MAUDE Adverse Event Report: UNKNOWN LIPPES LOOP IUD; IUD, DEVICE, INTRAUTERINE, CONTRACEPTIVE AND INTRODUCER, IMPLANT

Device Problem Defective Component (2292)

Patient Problems Renal Failure (2041); Scar Tissue (2060)

Event Type  No Answer Provided  

Event Description

Injured by lippy loop 1971 string for removal cut inside me.Constant exploratory for scar tissue then move surgeries for scar/tissue from previous surgery.Eczemas, addictive to steroids to treat eczema, kidney failure.Date (b)(6) 1971, birth control.Libby loop found to be defective.Mid 80's listed as medical device then because pharmaceutical.(b)(4) received a large payment in the mid 80's.It seems that the same product came back on the market many times as a pharmaceutical, under different names.Each time the product came back and was proved to be defective did (b)(4) get a large check every time? they also got paid for every surgery and treatment.How do justify the fact that so many people were injured after the iud was found to be defective.I have suffered with the problems caused by this defective product for almost 50 years.Fda approval is a gold star endorsement a product can't get on to the market without it.In all fairness you should buy insurance so that the poor people who are injured by your mistakes can be compensated.Did you really not know that this product has been maming people for 50 years? you owe me.You don't want to pay.I can't make you pay however please check and see if medical providers actually made a business of maming people and collecting from the manufacturer.If they are suing every iud manufacturer for the same type of injury over and over.It is your fault however if medical providers keep suing over and over for the same type of injury it is a crime.You really should be ashamed of that you have failed to protect me and million's of young women.

• Brand Name: LIPPES LOOP IUD
• Type of Device: IUD, DEVICE, INTRAUTERINE, CONTRACEPTIVE AND INTRODUCER, IMPLANT
• Manufacturer (Section D): UNKNOWN
• MDR Report Key: 9818602
• MDR Text Key: 183620957
• Report Number: MW5093677
• Device Sequence Number: 1
• Product Code: HDT
• Combination Product (y/n): N
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Voluntary
• Reporter Occupation: Other
• Type of Report: Initial
• Report Date: 12/27/2018

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: No
• Device Operator: No Information
• Initial Date Manufacturer Received: Not provided
• Initial Date FDA Received: 03/10/2020
• Type of Device Usage: N
• Patient Sequence Number: 1
• Patient Weight: 68