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FDA Medical Device Recalls (openFDA)

Praxair Distribution Inc.: Praxair Grab ''n Go Vantage unit, model PRX-9496.

Recall number
Z-0580-06
Recalling firm
Praxair Distribution Inc.
Product
Praxair Grab ''n Go Vantage unit, model PRX-9496.
Status
Terminated
Initiated
2005-12-21
Posted
2006-03-01
Terminated
2008-10-29
Reason
The units may experience a delay in oxygen flow upon initial actuation.
Root cause
Other
Action
The recalling firm sent a recall letter, dated 12/21/05, to all consignees.
Quantity
2,486 units of models PRX-9495 and PRX-9496 combined
Distribution
The product was distributed to 27 institutions and 2 distributors located in OH, MA, IL, CA, UT, PA, MD, and IN and to 2 institutions in Canada: Moncton, NB and Ottawa, ON.
Lot, serial or model codes
All codes (product manufactured from March, 2005 to the present)
510(k) numbers
not on file
PMA numbers
not on file
Product code
CAN
Firm FEI
3005503166
Firm city
Middleburg Heights
Firm state
OH
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

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

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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