Product Safety Recalls

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Aizu Olympus Co., Ltd. Recall 90664

Description: EVIS EXERA III Bronchovideoscope

Aizu Olympus Co., Ltd. Recall 90664 Information

Mandated?Voluntary: Firm initiated
Recall NumberZ-1559-2022
Event ID90664
Event DescriptionEVIS EXERA III Bronchovideoscope
Product TypeDevices
DistributionUS Nationwide distribution in the states of FL, IL, NC, PA & TX.
Recall ReasonThe recalled unit was utilized in a veterinary endoscopy procedure in advance of being assigned to healthcare facilities as a loaner.
Device Classification20220831
Device Code InfoUDI-DI: 04953170342134; Serial No. 2911858; Model No. BF-XP190.
Center Classification Date20220819
Recall Initiation Date20220720
Recalling FirmAizu Olympus Co., Ltd.
Initial Notification E-Mail
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