Medical Device Recalls
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510(K) Number: K071698 |
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| Aurora Series, Aurora 7 lighthead; Models: LED7 (including TV models). The Aurora Series is intend... | 2 | 08/14/2024 |
FEI # 3006437518 DKK Dai-Ichi Shomei Co., Ltd. |
| Aurora 4 Series, Aurora 7 lighthead; Models: AUA7 (including TV models). The Aurora Series is inten... | 2 | 08/14/2024 |
FEI # 3006437518 DKK Dai-Ichi Shomei Co., Ltd. |
| Aurora 3 Series, Aurora 7 lighthead; Models: AUT7 (including TV models). The Aurora Series is inten... | 2 | 08/14/2024 |
FEI # 3006437518 DKK Dai-Ichi Shomei Co., Ltd. |
| Aurora 2 Series, Aurora 7 lighthead; Models: AUR7 (including TV models). The Aurora Series is intend... | 2 | 08/14/2024 |
FEI # 3006437518 DKK Dai-Ichi Shomei Co., Ltd. |
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