Zimmer Dental recalls

Zimmer Dental has 33 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 12 Sep 2018.

Total recalls33since 2014

Last 12 months0reported

Class I00% of total

Ongoing0latest 12 Sep 2018

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 0 0Nov 0 0 0Feb 0 0 0May 0 0 0Aug 0 0

Severity split

Class I 0 0%Class II 33 100%Class III 0 0%

Why zimmer dental is recalled

Product types

By year

201839%
20171339%
20161339%
201513%
201439%

All zimmer dental recalls, newest first

33 total

Reported	Class	Recall	Company	Reason	Where
12 Sep 2018Device	CLASS II	Outer Package Label: Tapered Screw-Vent Implant System recalled	Zimmer Dental	Packaging Defects	Nationwide
4 Apr 2018Device	CLASS II	Tapered Screw-Vent MTX, Dental Implant, sterile recalled	Zimmer Dental	Labeling Errors	Nationwide
4 Apr 2018Device	CLASS II	Tapered Screw-Vent MTX, Dental Implant, sterile recalled	Zimmer Dental	Labeling Errors	Nationwide
27 Dec 2017Device	CLASS II	Instrument Kit System, Tapered Screw-Vent Implant System recalled	Zimmer Dental	Other	Nationwide
27 Dec 2017Device	CLASS II	Instrument Kit System, Tapered Screw-Vent Implant System recalled	Zimmer Dental	Other	Nationwide
27 Dec 2017Device	CLASS II	Tapered SwissPlus & SwissPlus Implant Systems surgical kit recalled	Zimmer Dental	Other	Nationwide
27 Dec 2017Device	CLASS II	Tapered Screw-Vent MTX recalled by Zimmer Dental	Zimmer Dental	Device Malfunction	CA
27 Dec 2017Device	CLASS II	GemLock RHD2.5 Hex Driver recalled by Zimmer Dental	Zimmer Dental	Other	Nationwide
4 Oct 2017Device	CLASS II	Thread Retrieval Drill recalled by Zimmer Dental	Zimmer Dental	Other	CA
4 Oct 2017Device	CLASS II	Impression Cap Cont recalled by Zimmer Dental	Zimmer Dental	Other	CA
4 Oct 2017Device	CLASS II	Try-in,abutment, Cont recalled by Zimmer Dental	Zimmer Dental	Other	CA
4 Oct 2017Device	CLASS II	Waxing Coping, Cont,ang recalled by Zimmer Dental	Zimmer Dental	Other	CA
4 Oct 2017Device	CLASS II	Abut Gold Friction-fit recalled by Zimmer Dental	Zimmer Dental	Other	CA
4 Oct 2017Device	CLASS II	Guide Sleeve recalled by Zimmer Dental	Zimmer Dental	Other	CA
4 Oct 2017Device	CLASS II	Implant,1-pc,ang,3.0x10mm recalled by Zimmer Dental	Zimmer Dental	Other	CA
26 Apr 2017Device	CLASS II	Tapered SwissPlus Implant System recalled by Zimmer Dental	Zimmer Dental	Other	CA
17 Feb 2016Device	CLASS II	Implant,TM, Mtx Full diameter recalled by Zimmer Dental	Zimmer Dental	Foreign Material	Nationwide
17 Feb 2016Device	CLASS II	Implant,TM, Mtx Full diameter recalled by Zimmer Dental	Zimmer Dental	Foreign Material	Nationwide
17 Feb 2016Device	CLASS II	Implant,TM, Mtx Full diameter recalled by Zimmer Dental	Zimmer Dental	Foreign Material	Nationwide
17 Feb 2016Device	CLASS II	Implant,TM, Mtx Full diameter recalled by Zimmer Dental	Zimmer Dental	Foreign Material	Nationwide
17 Feb 2016Device	CLASS II	Implant,TM, MTX diameter recalled by Zimmer Dental	Zimmer Dental	Foreign Material	Nationwide
17 Feb 2016Device	CLASS II	Implant,TM, Mtx Full x diameter recalled by Zimmer Dental	Zimmer Dental	Foreign Material	Nationwide
17 Feb 2016Device	CLASS II	Implant,TM, MTX diameter recalled by Zimmer Dental	Zimmer Dental	Foreign Material	Nationwide
17 Feb 2016Device	CLASS II	Implant,TM, MTX diameter recalled by Zimmer Dental	Zimmer Dental	Foreign Material	Nationwide
17 Feb 2016Device	CLASS II	Implant,TM, Mtx Full x diameter recalled by Zimmer Dental	Zimmer Dental	Foreign Material	Nationwide
17 Feb 2016Device	CLASS II	Implant,TM, MTX diameter recalled by Zimmer Dental	Zimmer Dental	Foreign Material	Nationwide
17 Feb 2016Device	CLASS II	Implant,TM, MTX x diameter recalled by Zimmer Dental	Zimmer Dental	Foreign Material	Nationwide
17 Feb 2016Device	CLASS II	Implant,TM, MTX x diameter recalled by Zimmer Dental	Zimmer Dental	Foreign Material	Nationwide
17 Feb 2016Device	CLASS II	Implant,TM, Mtx Full diameter recalled by Zimmer Dental	Zimmer Dental	Foreign Material	Nationwide
18 Feb 2015Device	CLASS II	GemLock Long Hex Driver recalled by Zimmer Dental	Zimmer Dental	Device Malfunction	CA

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.