Overview of recall records associated with Capso Vision, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 3.
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…
Possible mis-labeling of the device with incorrect serial number labels which may result in a patient's misdiagnosis.
Capsule Endoscopy System: a defect present in the capsule window may be stressed through the production process and in the final package, which could cause the housing of the capsule to…
This page summarizes recall records in which the official source identifies Capso Vision, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
