Gyrus Acmi, Incorporated recalls

Gyrus Acmi, Incorporated has 6 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 6 Jun 2018. The most frequent reason is sterility.

Total recalls6since 2012

Last 12 months0reported

Class I00% of total

Ongoing0latest 6 Jun 2018

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 6 100%Class III 0 0%

Why gyrus acmi, incorporated is recalled

Sterility583%
Lead & Heavy Metals117%

Product types

Other Medical Devices583%
Surgical Instruments117%

By year

2018117%
2015233%
2014117%
2013117%
2012117%

All gyrus acmi, incorporated recalls, newest first

6 total

Reported	Class	Recall	Company	Reason	Where
6 Jun 2018Device	CLASS II	Reusable Active Cord for Bovie/ValleyLab Generators recalled	Gyrus Acmi, Incorporated	Sterility	Nationwide
17 Jun 2015Device	CLASS II	Diego Elite Tubeset recalled by Gyrus Acmi, Incorporated	Gyrus Acmi, Incorporated	Sterility	Nationwide
17 Jun 2015Device	CLASS II	Diego Elite Tubeset, intended for cutting, coagulation recalled	Gyrus Acmi, Incorporated	Sterility	Nationwide
3 Dec 2014Device	CLASS II	Disposable Falope-Ring Band Applicator Kits recalled	Gyrus Acmi, Incorporated	Lead & Heavy Metals	Nationwide
12 Jun 2013Device	CLASS II	Myringotomy Knife Disposable, Sickle Blade Flat Handle recalled	Gyrus Acmi, Incorporated	Sterility	Nationwide
28 Nov 2012Device	CLASS II	Parparella-type Vent Tube, Silicone recalled by Gyrus Acmi, Incorporated	Gyrus Acmi, Incorporated	Sterility	KS

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.