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Richard Wolf Medical Instruments Recalls
9 recalls on record · November 13, 2013 to July 17, 2019 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
July 17, 2019Medical DevicesFDA
Richard Wolf Medical Instruments Corp. recalls E-Line Cutting Electrode 11.5Fr Mono 0 degrees, Sterile. One electrode is placed in a plastic tray and then inserted in
Hazard: E-Line Cutting Electrode package 8416.0305 contains E-Line Hook Electrode 8416.09 instead of E-Line Cutting Electrode 8416.03.
August 31, 2016Medical DevicesFDA
Richard Wolf Medical Instruments Corp. recalls Conical portio adapter (acorn) small & large are used for examination and diagnosis in conjunction with endoscopic acces
Hazard: The distal end of the Conical portio adapter (acorn) is composed of a small cap (head) that partially sits inside a hollow shaft (tube). These two parts are welded together to create one piece. In the impacted batches of product, the weld was improperly performed. As a result, the two pieces are not properly joined. This potential failure can result in the separation of the two pieces. The possible separation of these two components presents a potential risk to patients.
March 23, 2016Medical DevicesFDA
Richard Wolf Medical Instruments Corp. recalls The Vesa 75/100 adaptation with rotation is an accessory to a surgical camera intended to be used to record operative pr
Hazard: Supplier of the "VESA 75 / 100 adaptation with rotation", which is part of their monitor mounts and support arms may be missing riveting.
February 17, 2016Medical DevicesFDA
Richard Wolf Medical Instruments Corp. recalls Reuseable rotary blade/abrader, product number 899751514. The oval burr frontally hooded is an attachment or accessory
Hazard: Weak weld in the reusable rotary blade/abrader (burr) may result in inner part breaks at the distal or proximal end making the product dysfunctional.
February 17, 2016Medical DevicesFDA
Richard Wolf Medical Instruments Corp. recalls Reuseable rotary blade/abrader, product number 899751504. The oval burr laterally hooded is an attachment or accessory
Hazard: Weak weld in the reusable rotary blade/abrader (burr) may result in inner part breaks at the distal or proximal end making the product dysfunctional.
February 17, 2016Medical DevicesFDA
Richard Wolf Medical Instruments Corp. recalls Reuseable rotary blade/abrader, product number 899751305. The round burr is an attachment or accessory to the air-powe
Hazard: Weak weld in the reusable rotary blade/abrader (burr) may result in inner part breaks at the distal or proximal end making the product dysfunctional.
March 11, 2015Medical DevicesFDA
Richard Wolf Medical Instruments Corp. recalls The I-Cart is used to store, transport, and power video equipment used in medical procedures.
Hazard: The transformers installed on carts used for Richard Wolf medical video systems may overheat causing smoke and black plastic material to leak from the cart chassis.
October 15, 2014Medical DevicesFDA
Richard Wolf Medical Instruments Corp. recalls The Hulka Clip is a sterile packaged medical device that carries a two year expiration date. It is packaged two clips pe
Hazard: Richard Wolf Medical Instrument Corporation is recalling Hulka Clip Tubal Occluding Device lot 51000232. The devices are being recalled as a part of an investigation into a biocompatibility test discrepancy where the recalled lot (lot 51000232) passed final release testing, but the subsequent lot failed biocompatibility testing on a component that was also used to manufacture lot 51000232.
November 13, 2013Medical DevicesFDA
Richard Wolf Medical Instruments Corp. recalls Individual units labeled in part: REF: 4630022; for S(a)line resectoscopes; Vaporization electrode, sterite; 4mm telesco
Hazard: Richard Wolf Medical Instrument Corporation recieved a complaint stating that a 4630024 vaporization electrode was packaged in a 4630022 pouch.