Device recalls

Achieva 1.5T Initial system Model Number (REF): 781178

Philips North America Llc · The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's tech…

Open, ClassifiedUnder Investigation by firmZ-1838-2024
Open FDA's page for this record
Cfres ID
207343
Product res number
Z-1838-2024
Event date initiated
2024-05-03
Event date posted
2024-05-17
Recall status
Open, Classified
Res event number
94508
Product code
LNH
Product description
Achieva 1.5T Initial system Model Number (REF): 781178
Code info
UDI-DI: N/A Serial Numbers: 20282, 20303
Firm FEI number
3016618143
Recalling firm
Philips North America Llc
Address 1
222 Jacobs St
City
Cambridge
State
MA
Postal code
02141-2289
Additional info contact
Customer Care Solution Center 800-722-9377
Root cause description
Under Investigation by firm
Product quantity
2 units
Reason for recall

The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's technical room, resulting in Smoke and/or fire

Action

Philips issued Urgent Medical Device Correction notifications to customers on 22-Apr-2024 via FedEx . Philips Markets Organizations are responsible for distributing the letters outside of the US. Letter states reason for recall, health risk and action to take: If a smoke/fire alarm is detected: a. Immediately stop scanning and evacuate the patient and staff from the examination room. b. If a developing fire is detected, adhere to established hospital fire emergency procedures, which may include switching off power to the complete system and/or removing the magnet field by using the Emergency Magnet Off button. c. Do not attempt to continue scanning. d. Immediately contact Philips Service. " Ensure all users are aware of facility specific Emergency Procedures as outlined in Chapter 2: Safety in the Instructions for Use Emergency procedures The User is required to establish emergency procedures for the following situations: " A medical emergency " A fire " An emergency that requires immediate removal of the magnetic field " The release of helium gas into the examination room Philips MRI systems have an Emergency Table Stop button in case there is an emergency during tabletop movement. " Circulate this Urgent Medical Device Correction Letter to all users of this device so that they are aware of the issue. " Post this notice near the affected MR system(s) for ease of reference. Please complete and return the attached response form to Philips promptly and no later than 30 days from receipt via email to: pd.cnr@philips.com. Completing this form confirms receipt of the Urgent Medical Device Correction Letter, understanding of the issue, and required actions to be taken. 5. The actions planned by Philips to correct the problem Philips will contact you to schedule time for a Field Service Engineer (FSE) to visit your site to inspect the g-MDU connections in the technical room and apply the proper torque to the connection if necessary.(reference FCO78100582). Philips plans t

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Austria, Belgium, Canada, China, Croatia, Czech Republic, Denmark, Finland, France, Germany, Greece, Italy, Japan, Lebanon, Libya, Lithuania, Martinique, Netherlands, Norway, Poland, Romania, Slovakia, Spain, Sweden, Switzerland, Thailand, United Kingdom.

K numbers
K193215
Harmonized identifiers (openFDA)
Device name
System, Nuclear Magnetic Resonance Imaging
Medical specialty description
Radiology
Regulation number
892.1000
Device class
2
K number
K222387, K183274, K905833, K915601, K914012, K212233, K092925, K010850, K944979, K943800, K083533, K891543, K930709, K141472, K093984, K153324, K162403, K230187, K901818, K994351, K002420, K923948, K261758, K883872, K930544, K020289, K111803, K203653, K884603, K921098, K930122, K914114, K120487, K944070, K994282, K062454, K896647, K913673, K900286, K040444 +1,070 more
PMA number
P830076, P830074, P860010, P840007, P830051, P830081, P840063, P860062, P830053, P850043, P830052
Registration number
3021059265, 3014232555, 3018423337, 3008156140, 3002808157, 3005049692, 3010398867, 2520313, 3013875850, 3015223550, 3032109225, 3014680716, 1055916, 3009196578, 1526534, 3008632256, 3026047529, 3033536331, 2126677, 3012761544, 1723170, 3003494057, 1058584, 3008986341, 1529041, 3012354318, 3010701021, 3010326005, 3010703925, 3036666444, 3004994584, 3032109181, 1650907, 3007350713, 3007562060, 3008284470, 3027373189, 3010009632, 2134213, 3004859018 +110 more
FEI number
3021059265, 1000571342, 3014232555, 3018423337, 1000114111, 3008156140, 3002808157, 3005049692, 3010398867, 2520313, 3001814065, 3013875850, 3015223550, 3032109225, 3014680716, 3009196578, 1526534, 3008632256, 3026047529, 3033536331, 2126677, 3012761544, 3003494057, 3008986341, 3012354318, 3010701021, 3010326005, 3010703925, 3036666444, 3004994584, 3032109181, 3007562060, 3007350713, 3008284470, 3003190524, 1000403400, 3027373189, 3010009632, 3004859018, 3018094310 +110 more
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.