This correction applies to all GE Healthcare MRI systems with superconducting magnets: Discovery MR450, Discovery MR750,
FDA device recall Z-1035-2015 · posted 2015-02-18 · Terminated
Recall details
- Recalling firm
- GE Healthcare
- Reason for recall
- At certain sites, the MRU may not be connected to the magnet. In emergency situations, a disconnected MRU could delay removal of a ferrous object from the magnet, potentially resulting in life-threatening injuries. The MRU must be connected to the magnet at all times.
- Action taken
- GE Healthcare sent an "Urgent Medical Device Correction" letter GEHC Ref# 60876 dated January 6, 2015 to affected consignees. The letter was addressed to Hospital Administrators / Risk Managers, Radiology Department Managers, & Radiologists. The letter described the Safety Issue, Safety Instructions, Affected Product Details, Product Correction & Contact Information. Customers were instructed to do the following: As a preventative measure, confirm that MRU is connected to the magnet by performing the following four step test on the MRU. 1. Verify the green CHARGER POWER LED is lit. 2. Depress and hold the TEST BATTERY switch for 15 seconds. The green BATTERY TEST LED should light and remain lit while the TEST BATTERY switch is depressed. 3. Place the TEST HEATER toggle switch in the A position. The green HEATER TEST LED should light. If it does not light, depress TEST HEATER LED switch to verify that the LED is functioning. 4. Place the TEST HEATER toggle switch in the B position. Green HEATER TEST LED should light. If it does not light, depress TEST HEATER LED switch to verify that the LED is functioning. If the MRU test does not perform as described in each of the 4 steps above, GEHC strongly recommends that you stop using the system, and immediately call your GEHC representative. Customers with questions may contact their local service representative. For questions regarding this recall call 1-800-437-1171.
- Root cause
- Employee error
- Status
- Terminated
- Product code
- LNH
- Quantity affected
- 12,968 (5,708 US, 7,260 OUS).
- Distribution
- Worldwide Distribution - US Nationwide in all states in continental USA including DC, PR, GU, and the countries of ALBANIA, ALGERIA, ARGENTINA, AUSTRALIA, AUSTRIA, AZERBAIJAN, BAHRAIN, BELARUS, BELGIU
- Date initiated
- 2015-01-07
- Date posted
- 2015-02-18
- Date terminated
- 2015-09-10
- Location
- Waukesha, WI
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| GE SIGNA EXCITE 1.5T MR SYSTEM, GE SIGNA EXCITE 3.0T MR SYSTEM (K041476) | Ge Medical Systems, LLC | 2004-06-17 |
| GE SIGNA 3.0T WITH EXCITE MR SYSTEM (K040444) | General Electric Co. | 2004-04-14 |
| GE 3.0T SIGNA INFINITY TWINSPEED WITH EXCITE MR SYSTEM (K030874) | General Electric Co. | 2003-03-28 |
| SIGNA INFINITY MR SYSTEM WITH EXCITE TECHNOLOGY (K013636) | GE Medical Systems | 2002-01-24 |
| 1.5T INFINITY TWINSPEED MR SYSTEM (K012200) | GE Medical Systems | 2001-08-03 |