Summary
The FDA issued a Class II for Ingenia 1.5T S Model Number (REF): 781347 by Philips North America Llc. Reason: 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 hospit.
Details
Source
Device Recall
External ID
Z-1847-2024
Action Date
2024-05-29
Status
Ongoing
Category
device
Product Description
Ingenia 1.5T S Model Number (REF): 781347
Lot/Code Info: UDI-DI: (01)00884838068421(21) Serial Numbers: 81003 81050 81051 81090 81111 81010 81027 81028 81030 81035 81063 81106 81093 81105 81116 81007 81004 81006 81009 81011 81016 81017 81018 81019 81020 81023 81024 81031 81037 81041 81055 81056 81057 81060 81062 81064 81070 81074 81078 81112 81115 81122 81146 81147 81153 81156 81158 81013 81044 81040 81047 81059 81167 81170 81171 81008 81108 81148 81133 81164 81001 81086 81079 81118 81138 81139 81140 81151 81175 81184 81069 81061 81065 81098 81085 81091 81092 81032 81043 81129 81131 81149 81155 81162 81165 81172 81180 81084 81087 81088 81094 81095 81100 81127 81132 81174 81157 81176 81071 81052 81067 81039 81038 81179 81185 81117 81173 81154 81025 81097 81152 81015 81029 81033 81034 81042 81046 81048 81049 81058 81072 81080 81103 81113 81123 81128 81137 81045 81075 81076 81077 81096 81114 81124 81126 81145 81159 81178
Quantity Affected: 139 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
Distribution
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.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-05-03
Company
Cambridge, MA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 291 device recalls issued in the same week, part of 403 device-related FDA actions this month.
Philips North America Llc has 302 FDA actions in our database, including 302 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Philips North America Llc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Philips North America Llc have FDA actions?
Philips North America Llc has 302 FDA actions in our database, including 302 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-1847-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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