InjuryISA
PIEZOWAVE2
Received Nov 24, 2025 · Event occurred Oct 1, 2025
Report 9611102-2025-00059 · MDR key 23633150
Device
Generic name
Piezowave 2 Control Unit
Manufacturer
Richard Wolf GmbhModel number
100505Catalog number
100505
Product problems
- Adverse Event Without Identified Device or Use Problem
- Adverse Event Without Identified Device or Use Problem
Patient
NA · Unknown
- No Clinical Signs, Symptoms or Conditions
- No Clinical Signs, Symptoms or Conditions
Narrative
Description of Event or Problem
IT WAS REPORTED THAT A PIEZOWAVE 2 WAS USED ON A PATIENT FOR MYOFASCIAL ACOUSTIC COMPRESSION THERAPY (MYACT) ON THE LEFT LEG IN A MEDICAL FACILITY. THE PATIENT WAS SUBSEQUENTLY DIAGNOSED WITH AN ACUTE MENISCUS ROOT TEAR IN HER LEFT KNEE, CONFIRMED BY IMAGING, AS WELL AS PERSISTENT NEUROPATHIC SYMPTOMS; HOWEVER, BASED ON THE CURRENT CLINICAL ASSESSMENT AND AVAILABLE FINDINGS, A DIRECT CAUSAL LINK TO THE MYACT TREATMENT IS CONSIDERED UNLIKELY AND CANNOT BE CONFIRMED.