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FDA Medical Device Recalls (openFDA)

Civco Medical Instruments Co. Inc.: VirtuTRAX Instrument Navigator, 14 Ga VirtuTRAX

Recall number
Z-0396-2022
Recalling firm
Civco Medical Instruments Co. Inc.
Product
VirtuTRAX Instrument Navigator, 14 Ga VirtuTRAX
Status
Terminated
Initiated
2021-10-08
Posted
not on file
Terminated
2024-09-30
Reason
There is potential that the VirtuTRAX device will not tighten onto the instrument to be used.
Root cause
Device Design
Action
The firm distributed an "URGENT: MEDICAL DEVICE RECALL" notice on 10/21/2021 by email. The notice explained the problem and requested acknowledgement of the notice. Entities further distributing the products were directed to notify those to whom the devices were distributed. The firm will be replacing the units.
Quantity
9 boxes (5 units/box)
Distribution
Worldwide distribution - US Nationwide and the countries of Belgium, Canada, China (Mainland), China (Taiwan), Denmark, France, Germany, Italy, Japan, Netherlands, Singapore, South Korea, Spain, Thailand.
Lot, serial or model codes
Part Number 610-1153; UDI 00841436102285; Lot Numbers: A122182, A131167, A131689, A131691, A141823
510(k) numbers
["K092619"]
PMA numbers
not on file
Product code
IYO
Firm FEI
1937223
Firm city
Kalona
Firm state
IA
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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