Every recall we track for Richard Wolf GmbH — 10 in all — plus the complaints and injury reports the public filed about them.
Richard Wolf recalls PiezoWave 2 Control Units with serial numbers 5000553232-5000553506 due to potential capacitor failure causing smoke and burning smell. Affected units may require replacement.
Richard Wolf recalls FLEX GRASP FORCEPS 5FR WL 550MM with potential inability to open jaws when endoscope shaft bends 90 degrees. Affected units have specific lot numbers and product codes.
Richard Wolf recalls FLEX GRASP FORCEPS 6.6FR WL 550MM (Product #8736.685) due to potential inability to open forceps jaws when endoscope shaft bends 90 degrees, risking medical procedures.
Richard Wolf recalls FLEX GRASP FORCEPS 5FR WL 550MM (Product #828.051) due to potential inability to open forceps jaws when endoscope shaft bends 90 degrees. Affected units have specific lot numbers.
Richard Wolf recalls FLEX Biopsy Forceps 5FR WL 550MM with potential inability to open jaws when endoscope shaft bends 90 degrees. Affected units have specific lot numbers.
Richard Wolf recalls Cutting Electrode BIPO 24.5FR model 4653.1323 with BIVAP electrode risk. Affected units sold in 2021; stop using immediately.
Richard Wolf recalls TEM Tube Sets with small diameter tube material that may cause improper use during transanal endoscopic procedures. Affected units include Lot 32324159, Model 4170.801.
Richard Wolf recalls Texas Bronchoscope Tubes (model numbers 825200641-825211430) manufactured from Oct 2006 to Aug 2018 due to potential loosening of cemented areas, which could affect safety during medical procedures.
Richard Wolf recalls tube set model 4170.801 for transanal endoscopic surgery due to risk of mixed tube ends. Affected units have specific lot numbers.
