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FDA Medical Device Recalls (openFDA)

Compumedics Usa, Ltd: Nonin Xpod Oximeter model numbers 3011 and 3012, distributed for use with the Compumedics E-Series Digital Amplifier.

Recall number
Z-0653-05
Recalling firm
Compumedics Usa, Ltd
Product
Nonin Xpod Oximeter model numbers 3011 and 3012, distributed for use with the Compumedics E-Series Digital Amplifier.
Status
Terminated
Initiated
2005-02-24
Posted
2005-03-24
Terminated
2007-12-07
Reason
Under specific conditions, the housing of the pulse oximeter contected to the amplifier can become excessively warm causing a burn upon contact with skin.
Root cause
Other
Action
The firm initiated the recall on February 24, 2005 via letter with return response post card.
Quantity
1376 units
Distribution
Product was distributed nationwide and to the following foreign countries: Australia, Canada, Greece, Hong Kong, Hungary, India, Iran, Israel, Italy, Japan, Malaysia, Netherlands, New Zealand, Pillippines, Portugal, Saudi Arabia, Singapore, South Africa, Spain, Switzerland, Taiwan, Thailand, Turkey, and the United Kingdom.
Lot, serial or model codes
All codes
510(k) numbers
not on file
PMA numbers
not on file
Product code
GWQ
Firm FEI
3002716534
Firm city
El Paso
Firm state
TX
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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