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Kerr recalls

Kerr has 5 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 25 Jun 2014.

Total recalls5since 2012

Last 12 months0reported

Class I00% of total

Ongoing0latest 25 Jun 2014

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 5 100%Class III 0 0%

Why kerr is recalled

Other Reasons360%
Device Malfunction240%

Product types

Dental Devices480%
Other Medical Devices120%

By year

2014120%
2012480%

All kerr recalls, newest first

5 total

Reported	Class	Recall	Company	Reason	Where
25 Jun 2014Device	CLASS II	Tytin Regular Set, Double Spill recalled by Kerr	Kerr	Other	Nationwide
28 Nov 2012Device	CLASS II	BioPlant, a dental bone grafting material recalled by Kerr	Kerr	Device Malfunction	Nationwide
28 Nov 2012Device	CLASS II	The name of the device is Laser Loupes, a dentalloupe recalled by Kerr	Kerr	Device Malfunction	Nationwide
28 Nov 2012Device	CLASS II	Freedom Cordless LED Light System recalled by Kerr	Kerr	Other	Nationwide
14 Nov 2012Device	CLASS II	The name of the device is AlgiNot, a dental impression material recalled	Kerr	Other	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.