Richard Wolf recalls

Richard Wolf appears in 10 official U.S. recall notices indexed by RecallRadar, most recently on 2025-05-21.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• PiezoWave 2 Control Unit, Product Number 100506US, compact myofascial acoustic compression therapy device that enables treatment with piezo…
  FDA Device · Class II · 2025-05-21 · Richard Wolf
• FLEX. BIOPSY FORCEPS 5FR WL 550MM, Product Number 829.051
  FDA Device · Class II · 2023-05-03 · Richard Wolf
• FLEX. GRASP. FORCEPS 5FR WL 550MM, Product Number 828.051
  FDA Device · Class II · 2023-05-03 · Richard Wolf
• FLEX. GRASP. FORCEPS 5FR WL 550MM, Product Number 8735.685
  FDA Device · Class II · 2023-05-03 · Richard Wolf
• FLEX. GRASP. FORCEPS 6.6FR WL 550MM, Product Number 8736.685
  FDA Device · Class II · 2023-05-03 · Richard Wolf
• CUTTING ELECTRODE BIPO 24.5FR, REF 4653.1323
  FDA Device · Class II · 2021-08-18 · Richard Wolf
• Tube Set for TEM - Product Usage: Transanal Endoscopic Microsurgery (TEM) combination system and the instrument set for the TEM procedure a…
  FDA Device · Class II · 2020-08-05 · Richard Wolf
• Richard Wolf Bronchoscope Tubes, Model Texas
  FDA Device · Class II · 2019-02-13 · Richard Wolf
• Artholine Punch B 4, 6MM H 1, 6MM, used for the removal of soft tissue, cartilage tissue or other non-osseous tissue via natural or surgica…
  FDA Device · Class II · 2018-08-29 · Richard Wolf
• RICHARD WOLF TUBE SET FOR TEM, REF 4170.801
  FDA Device · Class II · 2018-05-23 · Richard Wolf