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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 7 of 7 Results
Related Medical Device Recalls
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Z-2228-2023 - Flexiva Pulse 242 Single-Use Laser Fibers-intended to be used as a device that transmits Ho:YAG laser energy from cleared laser consoles to urological anatomy. Single-pack UPN : M006L8405910 2 07/21/2023 Boston Scientific Corporation
Z-2229-2023 - Flexiva Pulse 242 TracTip Single-Use Laser Fibers - intended to be used as a device that transmits Ho:YAG laser energy from cleared laser consoles to urological anatomy Single-pack UPN : M006L8405960... 2 07/21/2023 Boston Scientific Corporation
Z-2230-2023 - Flexiva Pulse 242 TracTip Single-Use Laser Fibers -intended to be used as a device that transmits Ho:YAG laser energy from cleared laser consoles to urological anatomy. 5-pack UPN: M006L8405961 2 07/21/2023 Boston Scientific Corporation
Z-2234-2023 - Flexiva Pulse ID 242 TracTip single Use Fiber-intended to be used as a device that transmits Ho:YAG laser energy from cleared laser consoles to urological anatomy 5-pack UPN: M006L8406961 2 07/21/2023 Boston Scientific Corporation
Z-2232-2023 - Flexiva Pulse ID-intended to be used as a device that transmits Ho:YAG laser energy from cleared laser consoles to urological anatomy (Box of 5)UPN: M006L8406911 2 07/21/2023 Boston Scientific Corporation
Z-2233-2023 - Flexiva Pulse 242 ID Trac Single Use Fiber-intended to be used as a device that transmits Ho:YAG laser energy from cleared laser consoles to urological anatomy (Single-pack UPN): M006L8406960 2 07/21/2023 Boston Scientific Corporation
Z-2231-2023 - Flexiva Pulse ID-intended to be used as a device that transmits Ho:YAG laser energy from cleared laser consoles to urological anatomy Single-pack UPN: M006L8406910 2 07/21/2023 Boston Scientific Corporation
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