Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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Z-1175-06 - GYRUS ACMI PKS PlasmaSEAL Open Forceps, model 2103PK and 917015PK. Sterile EO. The device is intended to be used with the PlasmaKinetic electrosurgical generator, software version 1.93 or greater or... | 2 | 06/27/2006 | Gyrus Medical, Inc. |
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