FDA recall Z-2536-2020

Capso Vision, Inc. · Class II · device

Product

The CapsoCam Plus (SV-3); Device Common Name: System, Imaging, Gastrointestinal, Wireless, Capsule; Catalog Number 2795 - Product Usage: intended for visualization of the small bowel mucosa in adults. It may be used as a tool in the detection of abnormalities of the small bowel.

Reason for recall

Ingestible video capsule system has capsule with incorrect capture mode which will not record data when the capsule is ingested by patients. If used, there is a risk of delay of diagnosis and the patient may need to repeat the exam.

Distribution

US Nationwide distribution including in the states of AZ, CA, DE, MD, NJ, NY, SC, and VA.

Key facts

Status
Terminated
Initiation date
2020-02-26
Report date
2020-07-15
Termination date
2021-01-28
Voluntary/Mandated
Voluntary: Firm initiated
Location
Saratoga, CA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2536-2020