Recall Z-0527-2008
Baxter Healthcare Renal Div · initiated November 14, 2007
Product
Baxter RenalSoft v.2.0 Patient Management Software Suite - HD Module; clinical data management software; Baxter Healthcare Corporation, McGaw Park, Illinois 60085
Codes / lots: Version 2.0 - HD Module, Serial Numbers 17023766 to 17026503
Reason for recall
Pre-Treatment/Post-Treatment Report errors: 1) The Heparin Bolus Value is displayed on Pre and Post Treatment Reports for patients with "No Heparin" orders (RenalSoft v2.0, Renal Software Suite v.3.0 and v.3.1), and 2) Withheld Medications are incorrectly displayed as Administered on the Pre-Treatment report (RenalSoft v.2.0 only).
FDA-determined cause: Software design
Action taken
Baxter Healthcare Corporation sent an Urgent Device Correction letter, dated 11/14/07, to all of the affected customers, informing them of the Heparin Bolus and the Withheld Medication issues and provided them with interim mitigation instructions that they should implement while waiting for a software correction. A Baxter representative will contact the customer to schedule the software update when the upgraded software is released. Customers were requested to complete and return the enclosed Customer Reply Form, indicating that they have disseminated the information to their staff, and indicating if they still have RenalSoft software and require an upgrade. Any questions were directed to Baxter Global Technical Services at 1-800-553-6898, option 4. A follow-up letter dated 3/6/08 was sent to the consignees on the same date, informing them that the upgraded RenalSoft Software v.2.0.1 was now available for installation. The consignees were requested to complete and fax back the customer reply form indicating that they received the letter, and were informed that they would be contacted by a Baxter representative to schedule an installation of the software upgrade at no charge.
Details
- Recall number
- Z-0527-2008
- Initiated
- November 14, 2007
- Posted by FDA
- January 26, 2008
- Terminated
- February 3, 2010
- Product code
- KPF – System, Dialysate Delivery, Semi-Automatic, Peritoneal
- Quantity
- 25 units
- Distribution
- Worldwide Distribution-USA including Puerto Rico, and countries of Australia, Austria, Canada, Chile, Denmark, Finland, Greece, Ireland, Italy, Mexico, The Netherlands, New Zealand, Norway, Panama, Portugal, Spain, Sweden and the United Kingdom
- Recalling firm
- Baxter Healthcare Renal Div, Park, IL
Other products in the same recall event
| Recall | Product | Initiated |
|---|---|---|
| Z-0528-2008 | Baxter Renal Software Suite v.3.0 and v.3.1 - Renal Link HD Module; clinical data…Pre-Treatment/Post-Treatment Report errors: 1) The Heparin Bolus Value is displayed on Pre and Post… | 11/14/2007Terminated |