Kerr Corporation: 5 recalls on record
Recalls filed with 1 agency: FDA (5).
First recall on record: November 14, 2012. Most recent: June 25, 2014.
Risk classification: Class II: 5
Most recent recalls
| Date | Agency | Product | Recall number |
|---|---|---|---|
| June 25, 2014 | FDA | Tytin Regular Set, Double Spill, 50 Capsules, Part Number 29948, Lot Number 3-1294. Th…Z-1788-2014 | Z-1788-2014 |
| November 28, 2012 | FDA | BioPlant, a dental bone grafting material. BioPlant has been assigned the product code L…Z-0401-2013 | Z-0401-2013 |
| November 28, 2012 | FDA | Freedom Cordless LED Light System. Freedom System, Standard Length, Part Number 910863-1,…Z-0402-2013 | Z-0402-2013 |
| November 28, 2012 | FDA | The brand name of the device is Laser Loupes, a dentalloupe with laser eye protection. …Z-0414-2013 | Z-0414-2013 |
| November 14, 2012 | FDA | The brand name of the device is AlgiNot, a dental impression material. Product …Z-0268-2013 | Z-0268-2013 |
Questions about this company
- How many recalls does Kerr Corporation have?
- Recalert has 5 U.S. recalls on record for Kerr Corporation, published between November 14, 2012 and June 25, 2014.
- What was the most recent Kerr Corporation recall?
- FDA recall Z-1788-2014, published June 25, 2014: Tytin Regular Set, Double Spill, 50 Capsules, Part Number 29948, Lot Number 3-1294. The intended use of this device is to be used as a dental restorative material in the treatment of dental caries.
- Which agencies have handled Kerr Corporation recalls?
- Kerr Corporation appears as the recalling firm in recalls from: FDA (5).
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