Richard Wolf Medical Instruments Corp.

FDA recalling firm · 7 enforcement events · 9 product records · 2013–2019 · IL

Richard Wolf Medical Instruments Corp. has 7 FDA enforcement events on this register (9 product records) between 2013 and 2019: 7 device; the busiest year was 2014 with 2.

0% of its events are Class I; the most common class is Class II (7). 0 events are listed as ongoing; the recalling firm's address is in IL.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

Initiated	Product (first record)	Type	Class	Records	Status
23 May 2019	E-Line Cutting Electrode 11.5Fr Mono 0 degrees, Sterile. One electrode is placed in a plastic tray and then inserted into a Tyvek pouch. Five packaged electrodes are placed in a white box. Product Usage: Resectoscopes are used for endoscopically controlled ablation of tissue. They are used, in combination with…	Device	Class II	1	Terminated
19 May 2016	Conical portio adapter (acorn) small & large are used for examination and diagnosis in conjunction with endoscopic accessories in gynecological laparoscopy, to determine patency of the fallopian tubes.	Device	Class II	1	Terminated
29 Feb 2016	The Vesa 75/100 adaptation with rotation is an accessory to a surgical camera intended to be used to record operative procedures.	Device	Class II	1	Terminated
25 Nov 2015	Reuseable rotary blade/abrader, product number 899751305. The round burr is an attachment or accessory to the air-powered device intended for use during surgical procedures to cut hard tissue or bone and soft tissue. General hospital and plastic surgery use.	Device	Class II	3	Terminated
10 Dec 2014	The I-Cart is used to store, transport, and power video equipment used in medical procedures.	Device	Class II	1	Terminated
9 Jul 2014	The Hulka Clip is a sterile packaged medical device that carries a two year expiration date. It is packaged two clips per procedural tray. Theses procedural trays are then sealed in a Tyvek/Mylar pouch and packaged in a cardboard shipping carton with ten pouches in each shipping carton.	Device	Class II	1	Terminated
18 Sep 2013	Individual units labeled in part: REF: 4630022; for S(a)line resectoscopes; Vaporization electrode, sterite; 4mm telescope 30 25 / 12: only for continuous irrigation sheath 24,5 Fr.; LOT 426111; 2011/06; 2016/06; STERILE; RICHARD WOLF; Cartons of 3 units labeled in part: REF 46300223; Vaporization electrode, sterile;…	Device	Class II	1	Terminated

By type and class

Device7

Class II7

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

Enforcement events for Richard Wolf Medical Instruments Corp. by year initiated.

Questions and answers

How many FDA recalls has Richard Wolf Medical Instruments Corp. had?

7 enforcement events (9 product records) on this register, 2013–2019: 7 device.

Are any Richard Wolf Medical Instruments Corp. recalls ongoing?

0 events are listed as ongoing in the current openFDA export.

What class are Richard Wolf Medical Instruments Corp. recalls?

7 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.