Medical Device Recalls
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510(K) Number: K133486 |
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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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| Bausch & Lomb Stellaris PC w/ Laser, BL14304 The responsible firm name is Bausch & Lomb Incorporate... | 2 | 12/23/2014 | Bausch & Lomb Inc |
| Bausch & Lomb Stellaris PC w/ Laser Upgrade BL14334 (Stellaris PC w v4 Software) with BL2272 (Laser ... | 2 | 12/23/2014 | Bausch & Lomb Inc |
| Bausch & Lomb Stellaris PC w/ Laser Upgrade BL1433 (Stellaris PC w v3 Software) with BL2272 (Laser U... | 2 | 12/23/2014 | Bausch & Lomb Inc |
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