Richard Wolf Medical Instruments recalls

Richard Wolf Medical Instruments has 9 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 17 Jul 2019. The most frequent reason is foreign material.

Total recalls9since 2013

Last 12 months0reported

Class I00% of total

Ongoing0latest 17 Jul 2019

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 9 100%Class III 0 0%

Why richard wolf medical instruments is recalled

Product types

By year

2019111%
2016556%
2015111%
2014111%
2013111%

All richard wolf medical instruments recalls, newest first

9 total

Reported	Class	Recall	Company	Reason	Where
17 Jul 2019Device	CLASS II	E-Line Cutting Electrode Mono 0 degrees, Sterile recalled	Richard Wolf Medical Instruments	Foreign Material	Nationwide
31 Aug 2016Device	CLASS II	Conical portio adapter (acorn) small & large are used recalled	Richard Wolf Medical Instruments	Device Malfunction	26 states
23 Mar 2016Device	CLASS II	The Vesa 75/100 adaptation with rotation is an accessory to recalled	Richard Wolf Medical Instruments	Other	Nationwide
17 Feb 2016Device	CLASS II	Reuseable rotary blade/abrader, product number recalled	Richard Wolf Medical Instruments	Foreign Material	WA
17 Feb 2016Device	CLASS II	Reuseable rotary blade/abrader, product number recalled	Richard Wolf Medical Instruments	Foreign Material	WA
17 Feb 2016Device	CLASS II	Reuseable rotary blade/abrader, product number recalled	Richard Wolf Medical Instruments	Foreign Material	WA
11 Mar 2015Device	CLASS II	The I-Cart is used to store, transport recalled by Richard Wolf Medical	Richard Wolf Medical Instruments	Foreign Material	Nationwide
15 Oct 2014Device	CLASS II	The Hulka Clip is a sterile packaged medical device that recalled	Richard Wolf Medical Instruments	Sterility	Nationwide
13 Nov 2013Device	CLASS II	Individual units labeled in part recalled by Richard Wolf Medical	Richard Wolf Medical Instruments	Sterility	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.