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FDA Medical Device Recalls (openFDA)

Capso Vision, Inc.: CapsoCam Plus *** System, Imaging, Gastrointestinal, Wireless, Capsule, Electrical Rating 3.1V DC/10mA REF 2795 - Product Usage: The CapsoCam Plus video capsule system is 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.

Recall number
Z-2073-2020
Recalling firm
Capso Vision, Inc.
Product
CapsoCam Plus *** System, Imaging, Gastrointestinal, Wireless, Capsule, Electrical Rating 3.1V DC/10mA REF 2795 - Product Usage: The CapsoCam Plus video capsule system is 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.
Status
Terminated
Initiated
2019-07-03
Posted
not on file
Terminated
2021-01-28
Reason
Possible mis-labeling of the device with incorrect serial number labels which may result in a patient's misdiagnosis.
Root cause
Process control
Action
On 07/03/2019, the firm sent an "URGENT: Medical Device Voluntary Recall Letter" to customers via email informing them that this recall is being initiated due to the discovery of possible mis-labeling of the device packaging with an incorrect serial number label and that the firm is aware of one incident of incorrect serial number. Actions to be taken by customers are to ship back the affected capsules with serial numbers provided with the notification letter. Customer are asked to notify the Recalling Firm by email if they are experiencing inventory shortage and replacements will be shipped as soon as the firm is notified. For any the Recalling Firm directly with any concerns or questions at (408) 866-6358 Monday through Friday, 8:00 AM to 4:30 PM (Pacific Time), or at email address azimun.jamal@capsovision.com
Quantity
44 units
Distribution
US Nationwide distribution including in the states of FL, GA, NY, PA, and TX.
Lot, serial or model codes
Lot Number: 02-18-0036  Serial Number and UDI Codes: A00ZD4.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZD4.699;  A00ZJ2.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZJ2.699;  A00ZK2.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZK2.699;  A00ZM0.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZM0.699;  A00ZM3.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZM3.699;  A00ZN3.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZN3.699;  A00ZQ5.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZQ5.699;  A00ZW6.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZW6.699;  A01004.699 0100867770000209 13180921 17200921 1002-18-0036 21A01004.699;  A0100H.699 0100867770000209 13180921 17200921 1002-18-0036 21A0100H.699;  A0102J.699 0100867770000209 13180921 17200921 1002-18-0036 21A0102J.699;  A0104G.699 0100867770000209 13180921 17200921 1002-18-0036 21A0104G.699;  A0104U.699 0100867770000209 13180921 17200921 1002-18-0036 21A0104U.699;  A00ZD6.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZD6.699;  A00ZJ5.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZJ5.699;  A00ZK4.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZK4.699;  A00ZX4.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZX4.699;  A010AA.699 0100867770000209 13180921 17200921 1002-18-0036 21A010AA.699;  A00ZL7.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZL7.699;  A00ZL8.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZL8.699;  A0102T.699 0100867770000209 13180921 17200921 1002-18-0036 21A0102T.699  A010A8.699 0100867770000209 13180921 17200921 1002-18-0036 21A010A8.699;  A010TD.699 0100867770000209 13180921 17200921 1002-18-0036 21A010TD.699;  A00ZY5.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZY5.699;  A010QP.699 0100867770000209 13180921 17200921 1002-18-0036 21A010QP.699;  A010T9.699 0100867770000209 13180921 17200921 1002-18-0036 21A010T9.699;  A010UC.699 0100867770000209 13180921 17200921 1002-18-0036 21A010UC.699;  A00ZL4.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZL4.699;  A00ZN4.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZN4.699;  A00ZP5.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZP5.699;  A00ZQ4.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZQ4.699;  A00ZW9.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZW9.699;  A00ZY1.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZY1.699;  A00ZY4.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZY4.699;  A00ZY6.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZY6.699;  A00ZZ7.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZZ7.699;  A010N1.699 0100867770000209 13180921 17200921 1002-18-0036 21A010N1.699;  A00ZC7.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZC7.699;  A00ZG3.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZG3.699;  A00ZX7.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZX7.699;  A010PH.699 0100867770000209 13180921 17200921 1002-18-0036 21A010PH.699;  A00ZC2.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZC2.699;  A00ZC6.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZC6.699;  A00ZH4.699 0100867770000209 13180921 17200921 1002-18-0036 21A00ZH4.699
510(k) numbers
["K183192"]
PMA numbers
not on file
Product code
NEZ
Firm FEI
3008062894
Firm city
Saratoga
Firm state
CA
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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