FDA Adverse Event Summary report: N

HEYER-SCHULTE MAMMARY PROSTHESIS

MDR report key: 13494 · Received May 24, 1994

Report

Report Number
MW1002193
Date Received
May 24, 1994
Date of Event
November 19, 1984
Report Date
May 13, 1994
Manufacturer
MENTOR CORP.
Product Code
FTR
Report Source
Voluntary report
Reporter Location
SC, US
Reporter Occupation
ATTORNEY

Narratives

Description of Event or Problem · 1

RPTR COMPLAINS OF TUMORS, CAPSULAR CONTRACTURES, FATIGUE, ACHES AND PAINS IN JOINTS, ARTHRITIS, AUTOIMMUNE PROBLEMS, PHYSICAL IMPAIRMENT ON LEFT SIDE, LUNG CANCER, MUSCLE INFLAMMATION, CYSTITIS, INFECTION IN BREAST, TREMORS OR MUSCLE SPASMS, RUPTURED IMPLANTS, RASHES, SKIN ABNORMALITIES, BURNING PAIN IN CHEST, BREAST, ARMS, RIBS AND ABDOMEN, DRY MOUTH AND VAGINA, JOINT SWELLING AND TENDERNESS, ENLARGED LYMPH NODES, MUSCLE ACHES, PAINS AND WEAKNESS, PHOTOSENSITIVITY, SLEEP DISTURBANCE, EASY BRUISING, TROUBLE SWALLOWING, NIGHT SWEATS, NOSE AND MOUTH ULCERS, LOW GRADE FEVERS, AND TINGLING IN LEGS, ARMS AND ELSEWHERE. (SAME RPTR REFERRED TO IN 1002191 AND 1002192.)

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HEYER-SCHULTE MAMMARY PROSTHESIS Implant FTR MENTOR CORP. 4989 490

Patients

Seq Age Sex Outcome Treatment
1 * *