MultiDiagnost 4 - x-ray system, multi functional/universal system for general use.
FDA device recall Z-0586-03 · posted 2003-02-27 · Terminated
Recall details
- Recalling firm
- Philips Medical Systems
- Reason for recall
- INTERNAL SHORT CIRCUIT - MAY ALLOW FOR STAND AND TABLE TO MOVE SPONTANEOUSLY IN UPWARD OR DOWNWARD MOVEMENT
- Action taken
- The firm issued a letter dated January 10, 2003 to their customers advising of the problem and that a respresentative would be contacting customers to arrange a time to visit to install new interface board. This is being conducted under FCO 70800007
- Root cause
- Other
- Status
- Terminated
- Product code
- JAA
- Quantity affected
- 22 units
- Distribution
- The firm distributed to 22 hospitals/medical centers located in CA, FL, IA, IL, IN, KY, MN, MO, NC, ND, NY, OH, SC, TN, TX, VA, and WV.
- Date initiated
- 2003-01-10
- Date posted
- 2003-02-27
- Date terminated
- 2005-04-11
- Location
- Bothell, WA
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| PHILIPS MULTIDIAGNOST 4 (K961374) | Philips Medical Systems, Inc. | 1996-08-19 |