Kerr/Pentron recalls

Kerr/Pentron has 4 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 6 May 2020. The most frequent reason is device malfunction.

Total recalls4since 2013

Last 12 months0reported

Class I00% of total

Ongoing0latest 6 May 2020

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 4 100%Class III 0 0%

Why kerr/pentron is recalled

Product types

Other Medical Devices375%
Dental Devices125%

By year

2020125%
2019125%
2013250%

All kerr/pentron recalls, newest first

4 total

Reported	Class	Recall	Company	Reason	Where
6 May 2020Device	CLASS II	Nexus Universal with OptiBond Universal recalled by Kerr/Pentron	Kerr/Pentron	Lead & Heavy Metals	Nationwide
12 Jun 2019Device	CLASS II	Regimen 28 Day - Glutaraldehyde Sterilizing recalled by Kerr/Pentron	Kerr/Pentron	Sterility	21 states
25 Sep 2013Device	CLASS II	NX3 Try-In Gel recalled by Kerr/Pentron	Kerr/Pentron	Device Malfunction	Nationwide
17 Apr 2013Device	CLASS II	Kerr Maxcem Elite, self-etch/self-adhesive resin cement recalled	Kerr/Pentron	Device Malfunction	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.