Kerr Recalls
6 recalls on record · August 21, 2006 to June 25, 2014 · Medical Devices, Vehicle Equipment
Recalls by year
06
12
14
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
June 25, 2014Medical DevicesFDA
Kerr Corporation recalls Tytin Regular Set, Double Spill, 50 Capsules, Part Number 29948, Lot Number 3-1294. The intended use of this device i
Hazard: Kerr Corporation is recalling one (1) lot of Tytin Regular Set ( Part Number 29948, Lot Number 3-1294), because it may set faster than specified in the Directions for Use.
November 28, 2012Medical DevicesFDA
Kerr Corporation recalls The brand name of the device is Laser Loupes, a dentalloupe with laser eye protection. Laser Loupes have been assigned
Hazard: The firm initiated the recall for Laser Loupes because the ink used to mark which laser frequency each laser Loupe protects against may wipe off. The loupes work according to specification, but the marking may not permanently adhere to the device.
November 28, 2012Medical DevicesFDA
Kerr Corporation recalls Freedom Cordless LED Light System. Freedom System, Standard Length, Part Number 910863-1, Serial Numbers 77001000-770034
Hazard: The firm recalled the Freedom Cordless LED Headlight because some units were assembled with an incorrect component in the control board electronics that may cause some Freedom Cordless LED Headlight units to become warm to the touch; however, no skin damage will occur.
November 28, 2012Medical DevicesFDA
Kerr Corporation recalls BioPlant, a dental bone grafting material. BioPlant has been assigned the product code LYC (Bone Grafting Material, Syn
Hazard: The firm initiated the recall becaue disturbing the BioPlant product soon after it is placed may halt or delay the ossification process.
November 14, 2012Medical DevicesFDA
Kerr Corporation recalls The brand name of the device is AlgiNot, a dental impression material. Product Part Numb
Hazard: The firm recalled the product because it may cure harder than expected within the shelf life, which could result in a material that may be more difficult to remove. Use of this product on patients with loose teeth may result in possible tooth fracture or tooth extraction.
August 21, 2006Vehicle EquipmentNHTSA
Kerr Equipment recall
Hazard: THE WEARER OF A NONCOMPLIANT HELMET MAY BE SERIOUSLY INJURED OR KILLED FROM HEAD IMPACTS IN THE EVENT OF A CRASH.