Ultra-Filtration (UF) Removal Regulators(Rgltr Assy UF REM Molded Spare); a spare part used with Baxter''s System 1000,
FDA device recall Z-1253-06 · posted 2006-07-25 · Terminated
Recall details
- Recalling firm
- Baxter Healthcare Renal Div
- Reason for recall
- The UF Removal Regulators were assembled incorrectly. The mis-assembly results in a failure to successfully calibrate the instrument and begin patient therapy.
- Action taken
- Baxter sent Urgent Device Correction letters dated 06/21/06 to all System 1000, TINA, Altratouch, Arena and Aurora Hemodialysis Instrument customers who may have received the nonconforming assemblies via first class mail on the same date, to the attention of the Hemodialysis Administrator. The letters informed the accounts that the three lots of UF Removal Regulators were potentially assembled incorrectly. While these regulators are identical in appearance to properly assembled components, the mis-assembly results in a failure to successfully calibrate the instrument and begin patient therapy. Replacement regulators were included with the recall letter, and the accounts were requested to return the regulators from their previous shipment to Baxter using the enclosed mailing materials. The accounts were requested to complete the enclosed reply form indicating the number of units received and the number of units returned and acknowledging receipt of the letter and dissemination of the information to their staff and to other services of facilities, as applicable, and fax the sheet to 1-727-544-3025. Any technical questions were directed to Baxter Global Technical Services at 1-800-553-6898, prompt 3, option 2, choice 1.
- Root cause
- Other
- Status
- Terminated
- Product code
- KDI
- Quantity affected
- 569 units
- Distribution
- Worldwide Distribution including the states of Arizona, California, Connecticut, Florida, Georgia, Maryland, Missouri, Ohio, Oklahoma, Tennessee, Texas and Puerto Rico, and international distribution
- Date initiated
- 2006-06-21
- Date posted
- 2006-07-25
- Date terminated
- 2008-03-04
- Location
- Park, IL
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| CENTURION PRESSURE INJECTABLE EXTENSION SET (K103562) | Centurion Medical Products Corporation | 2011-06-23 |
| BAXTER ARENA HEMODIALYSIS DELIVERY SYSTEM, MODEL 1571278000 (K030099) | Baxter Healthcare Corp | 2003-06-17 |
| DRAKE WILLOCK SYSTEM & ALTRA TOUCH 1000 DIALYSIS DELIVERY SYSTEM (K970446) | Althin Medical AB an Affiliate of Baxter Intl | 1997-06-02 |
| DRAKE WILLOCK SYSTEM 1000 DIALYSATE DELIVERY SYST (K910215) | Cd Medical, Inc. | 1991-04-09 |