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FDA Medical Device Recalls (openFDA)

Baxter Healthcare Renal Div: Renalsoft software; Baxter Healthcare Corporation, McGaw Park, Illinois 60085

Recall number
Z-0902-04
Recalling firm
Baxter Healthcare Renal Div
Product
Renalsoft software; Baxter Healthcare Corporation, McGaw Park, Illinois 60085
Status
Terminated
Initiated
2004-04-12
Posted
2004-07-20
Terminated
2008-02-26
Reason
There are software anomalies present that may increase the possibility of a medication error if the dialysis clinic software is used to track, record, or coordinate the administration of medications.
Root cause
Other
Action
Baxter sent Urgent Device Correction letters dated 4/12/04 to the attention of the Dialysis Unit Administrator. Separate letters were sent to the Renalsoft customers and to the Renal Software Suite customers. The letters described the software anomalies associated with the software and provided interim workaround instructions until permanent corrective actions to these anomalies can be identified.
Quantity
16 units
Distribution
Nationwide
Lot, serial or model codes
product code RENLSFT, all software versions
510(k) numbers
["K990953"]
PMA numbers
not on file
Product code
KPF--
Firm FEI
3000210122
Firm city
Park
Firm state
IL
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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