Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K982590 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Kerr TempBond Clear, Part # 33351, 1717 West Collins Avenue, Orange, CA 92867. Intended for use ... | 3 | 10/23/2009 | Kerr Corp |
| TempBond Clear Syringes (base and catalyst kit), a temporary dental cement, Part Number 28637 | 2 | 09/23/2006 | Kerr Corp |
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