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FDA Medical Device Recalls (openFDA)

Nova Biomedical Corporation: Stat Profile Critical Care Xpress (CCX) Analyzer Catalog Number: 35942

Recall number
Z-0826-04
Recalling firm
Nova Biomedical Corporation
Product
Stat Profile Critical Care Xpress (CCX) Analyzer Catalog Number: 35942
Status
Terminated
Initiated
2004-03-30
Posted
2004-07-20
Terminated
2004-06-17
Reason
Incorrectly assembled pumps may result in inconsistent compression of the tubing causing erratic results or calibration problems
Root cause
Other
Action
Nova Biomedical notified users by telephone on 3/31/04 and conducted follow-up by letter either by email or fax. On-site visit will be scheduled to replace the pump assembly.
Quantity
35 units
Distribution
CA, IL, LA, MA ,NJ, NY, OH, PA, TX International: Italy ,England, Japan,Turkey., U.A.E., Greece, Thailand, Switzerland, Finland, Saudi Arabia, Italy, Mexico, Trinidad, Ireland, France, Cyprus, Czech Republic, ,Germany
Lot, serial or model codes
Domestic S/N: Y01C03200 Y01C03130 Y01104030 Y01104040 Y01104100 Y01104110 Y01304150 Y01304120 Y01104150 Y01104130 Y01104050 Y01104190 Y01104160 Y01104220 Y01204020 Y01204100 Y01204010 Y01204130 Y01204150 Y01204160 Y01703120 Y01304040 Y01304010 Y01304110  International S/N: Inst. S/N Y01204200 Y01304030 Y01304130 Y01304140 Y01304090 Y01304100 Y01104140 Y01204070 Y01204170 Y01104120 Y01C03150
510(k) numbers
["K022746"]
PMA numbers
not on file
Product code
CHL
Firm FEI
1219029
Firm city
Waltham
Firm state
MA
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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