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FDA Medical Device Recalls (openFDA)

Bard Access Systems, Inc: Ultra/Phonic Conductivity Gel, 20 ml. Each unit is a foil to foil pouch. Product is packaged 25 pouches per box.

Recall number
Z-0719-05
Recalling firm
Bard Access Systems, Inc
Product
Ultra/Phonic Conductivity Gel, 20 ml. Each unit is a foil to foil pouch. Product is packaged 25 pouches per box.
Status
Terminated
Initiated
2004-11-03
Posted
2005-04-22
Terminated
2005-04-22
Reason
Conductivity gel pouches, labeled as sterile, may not be sterile.
Root cause
Other
Action
All domestic consignees were notified by letter on 10/04/2004. All foreign consignees were notified by letter on 10/15/04.
Quantity
121 boxes
Distribution
Nationwide. Foreign distribution to: Austria; Bahrain, Belgium, Bermuda, Brazil, Canada, Greece, Hong Kong, Italy, Japan, Kuwait, Malaysia, Mexico, Norway, Oman, Pakistan, Portugal, Qatar, Saudi Arabia, Switzerland, Turkey, United Arab Emirates, United Kingdom.
Lot, serial or model codes
Product Code 9001C0200. Lot Numbers 021404-4, 010904, 091403, 060303, 050403, 011003, 071202, 111300, 120998, 021202, 100101, 112703, 011202, 091398, 080900, 060500.
510(k) numbers
not on file
PMA numbers
not on file
Product code
ITX
Firm FEI
3006260740
Firm city
Salt Lake City
Firm state
UT
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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