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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 96889

18 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
May 13, 2025
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Philips North America Llc

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

18 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 18

Product Name: SmartPath to dStream for 1.5T; Model Numbers: (1) 781260, (2) 782112, (3) 782146

Z-1788-2025
Recall number
Z-1788-2025
Initiated
May 13, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America Llc
Quantity
80 units (1 US, 79 OUS)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Code information

Model Numbers: (1) 781260, (2) 782112, (3) 782146; UDI-DI: (1) 00884838095076,(2) 00884838098886, (3) 00884838108691; Serial Numbers: (1) 10044, 10151, 10164, 10170, 11000, 11001, 11062, 11076, 12009, 18038, 18663, 18872, 18938, 20115, 20164, 20413, 21011, 21019, 21062, 21133, 21249, 21278, 21477, 21577, 21583, 21591, 21880, 21888, 22157, 22248, 32049, 32094, 32099, 32113, 32142, 32184, 32217, 32245, 32286, 32322, 32334, 32636, 32845, 39024, 5479, 5490, 8057, 8263, 8305, 8330, 8365, 8378, 8392, 8456, 8561, 8639, 8736, 8752, 8808, 8819, 8942, (2) 10479, 12002, 13024, 18651, 21205, 21685, 22267, 30031, 39106, (3) 13013, 20414, 21202, 21990, 22251, 32116, 32407, 32683, 33611, 39040;

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Andorra, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, Colombia, C¿te D'Ivoire, Cyprus, Czech Republic, Denmark, Finland, France, French Guiana, Georgia, Germany, Greece, Guadeloupe, Hong Kong, Iceland, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kenya, Latvia, Lebanon, Libya, Lithuania, Malaysia, Malta, Martinique, Mexico, Moldova, Monaco, Netherlands, New Zealand, Norway, Palestine, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., Serbia, Slovenia, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, Ukraine, United Kingdom, U.A.E.

device · product 2 of 18

Product Name: SmartPath to dStream for 3.0T; Model Number: 782145

Z-1789-2025
Recall number
Z-1789-2025
Initiated
May 13, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America Llc
Quantity
12 units (OUS only)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Code information

Model Number: 782145; UDI-DI: 00884838095083; Serial Numbers: 17377, 17385, 34114, 34208, 38118, 38170, 38294, 38313, 38336, 73002, 73004, 74004;

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Andorra, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, Colombia, C¿te D'Ivoire, Cyprus, Czech Republic, Denmark, Finland, France, French Guiana, Georgia, Germany, Greece, Guadeloupe, Hong Kong, Iceland, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kenya, Latvia, Lebanon, Libya, Lithuania, Malaysia, Malta, Martinique, Mexico, Moldova, Monaco, Netherlands, New Zealand, Norway, Palestine, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., Serbia, Slovenia, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, Ukraine, United Kingdom, U.A.E.

device · product 3 of 18

Product Name: SmartPath to dStream for XR and 3.0T; Model Numbers: (1) 781270, (2) 782113;

Z-1790-2025
Recall number
Z-1790-2025
Initiated
May 13, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America Llc
Quantity
55 units (2 US, 53 OUS)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Code information

Model Numbers: (1) 781270, (2) 782113; UDI-DI: (1) 00884838095083, (2) 00884838098909; Serial Numbers: (1) 17283, 17299, 17321, 17356, 17357, 17369, 17378, 17398, 17416, 17425, 17473, 17490, 17499, 17550, 17564, 17565, 17569, 17589, 17590, 17594, 23026, 24012, 24023, 24066, 24075, 24087, 24090, 24110, 34107, 34152, 35043, 35047, 35056, 38004, 38023, 38084, 38089, 38113, 38120, 38199, 38202, 38300, 38366, (2) 17252, 17258, 17346, 24039, 24077, 24146, 34131, 34212, 35071, 38197, 38234, 38291;

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Andorra, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, Colombia, C¿te D'Ivoire, Cyprus, Czech Republic, Denmark, Finland, France, French Guiana, Georgia, Germany, Greece, Guadeloupe, Hong Kong, Iceland, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kenya, Latvia, Lebanon, Libya, Lithuania, Malaysia, Malta, Martinique, Mexico, Moldova, Monaco, Netherlands, New Zealand, Norway, Palestine, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., Serbia, Slovenia, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, Ukraine, United Kingdom, U.A.E.

device · product 4 of 18

Product Name: SmartPath to Ingenia Elition X; Model Numbers: (1) 782118, (2) 782144;

Z-1791-2025
Recall number
Z-1791-2025
Initiated
May 13, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America Llc
Quantity
16 units (All OUS)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Code information

Model Numbers: (1) 782118, (2) 782144; UDI-DI: (1) 00884838099746, (2) 00884838108677; Serial Numbers: (1) 42072, 42194, 42306, 71019, 71025, 71050, 85661, 85676, (2) 42062, 42105, 42323, 42346, 42441, 71278, 71504, 71508;

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Andorra, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, Colombia, C¿te D'Ivoire, Cyprus, Czech Republic, Denmark, Finland, France, French Guiana, Georgia, Germany, Greece, Guadeloupe, Hong Kong, Iceland, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kenya, Latvia, Lebanon, Libya, Lithuania, Malaysia, Malta, Martinique, Mexico, Moldova, Monaco, Netherlands, New Zealand, Norway, Palestine, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., Serbia, Slovenia, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, Ukraine, United Kingdom, U.A.E.

device · product 5 of 18

Product Name: Upgrade to MR 7700; Model Number: 782130;

Z-1792-2025
Recall number
Z-1792-2025
Initiated
May 13, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America Llc
Quantity
13 units (7 US, 6 OUS)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Code information

Model Number: 782130; UDI-DI: 00884838104402; Serial Numbers: 42030, 42066, 42151, 42211, 42248, 42376, 45001, 45007, 45236, 71613, 71907, 85643, 85644;

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Andorra, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, Colombia, C¿te D'Ivoire, Cyprus, Czech Republic, Denmark, Finland, France, French Guiana, Georgia, Germany, Greece, Guadeloupe, Hong Kong, Iceland, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kenya, Latvia, Lebanon, Libya, Lithuania, Malaysia, Malta, Martinique, Mexico, Moldova, Monaco, Netherlands, New Zealand, Norway, Palestine, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., Serbia, Slovenia, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, Ukraine, United Kingdom, U.A.E.

device · product 6 of 18

Product Name: Evolution Upgrade 1.5T; Model Numbers: (1) 782116, (2) 782148;

Z-1793-2025
Recall number
Z-1793-2025
Initiated
May 13, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America Llc
Quantity
52 units (3 US, 49 OUS)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Code information

Model Numbers: (1) 782116, (2) 782148; UDI-DI: (1) 00884838099722, (2) 00884838108714; Serial Numbers: (1) 41042, 41047, 41080, 41139, 41229, 41287, 41295, 41327, 41367, 41424, 41432, 41433, 41457, 41568, 70068, 70284, 70630, 70696, 70995, 70996, 81021, (2) 41011, 41031, 41244, 41284, 41334, 41427, 41464, 41488, 41523, 41534, 41547, 70067, 70289, 70452, 70454, 70473, 70590, 70622, 70644, 70652, 70742, 70769, 70803, 70829, 70966, 70980, 84102, 84109, 84368, 84630, 84825;

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Andorra, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, Colombia, C¿te D'Ivoire, Cyprus, Czech Republic, Denmark, Finland, France, French Guiana, Georgia, Germany, Greece, Guadeloupe, Hong Kong, Iceland, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kenya, Latvia, Lebanon, Libya, Lithuania, Malaysia, Malta, Martinique, Mexico, Moldova, Monaco, Netherlands, New Zealand, Norway, Palestine, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., Serbia, Slovenia, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, Ukraine, United Kingdom, U.A.E.

device · product 7 of 18

Product Name: Evolution Upgrade 3.0T; Model Numbers: (1) 782117, (2) 782143;

Z-1794-2025
Recall number
Z-1794-2025
Initiated
May 13, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America Llc
Quantity
28 units (5 US, 23 OUS)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Code information

Model Numbers: (1) 782117, (2) 782143; UDI-DI: (1) 00884838099739, (2) 00884838108660; Serial Numbers: (1) 42023, 42024, 42078, 42375, 42402, 42408, 71348, 85675, 85687, 85694, 85705, (2) 42193, 42225, 42308, 42320, 42366, 42415, 71595, 71815, 71836, 85649, 85684, 85688, 85690, 85695, 85697, 85699, 85708;

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Andorra, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, Colombia, C¿te D'Ivoire, Cyprus, Czech Republic, Denmark, Finland, France, French Guiana, Georgia, Germany, Greece, Guadeloupe, Hong Kong, Iceland, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kenya, Latvia, Lebanon, Libya, Lithuania, Malaysia, Malta, Martinique, Mexico, Moldova, Monaco, Netherlands, New Zealand, Norway, Palestine, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., Serbia, Slovenia, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, Ukraine, United Kingdom, U.A.E.

device · product 8 of 18

Product Name: Ingenia 1.5T; Model Numbers: (1) 781315, (2) 781341, (3) 781396, (4) 782101, (5) 782115, (6) 782140;

Z-1795-2025
Recall number
Z-1795-2025
Initiated
May 13, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America Llc
Quantity
264 units (46 US, 218 OUS)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Code information

Model Numbers: (1) 781315, (2) 781341, (3) 781396, (4) 782101, (5) 782115, (6) 782140; UDI-DI: (1) 00884838099715, (2) 00884838055322, (3) 00884838009820, (4) 00884838098275, (5) 00884838099043, (6) 00884838108646; Serial Numbers: (1) 61003, 61005, 61007, 61014, 61022, 61023, 61024, 61029, 61031, 61033, 61036, 61045, 61051, 61052, 61053, 61054, 61055, 61057, 61059, 61062, 61063, 61076, 61088, 61093, 61097, 61101, 61112, 61124, (2) 70009, 70042, 70051, 70056, 70059, 70075, 70095, 70104, 70203, 70223, 70249, 70257, 70262, 70300, 70311, 70346, 70376, 70381, 70383, 70427, 70432, 70439, 70440, 70453, 70460, 70461, 70472, 70483, 70588, 70596, 70598, 70619, 70645, 70646, 70647, 70650, 70658, 70659, 70661, 70672, 70684, 70699, 70702, 70708, 70712, 70724, 70736, 70741, 70751, 70798, 70800, 70820, 70825, 70826, 70836, 70846, 70862, 70863, 70880, 70886, 70889, 70896, 70897, 70902, 70920, 70922, 70953, 70961, 70970, 70975, 70977, 70979, 70983, 70988, 70989, 84027, 84031, 84034, 84042, 84043, 84076, 84079, 84080, 84084, 84085, 84093, 84118, 84130, 84136, 84141, 84157, 84170, 84172, 84173, 84185, 84186, 84191, 84193, 84202, 84203, 84205, 84210, 84212, 84226, 84233, 84253, 84266, 84267, 84270, 84276, 84281, 84295, 84332, 84333, 84335, 84343, 84359, 84360, 84376, 84379, 84388, 84394, 84416, 84419, 84429, 84431, 84448, 84462, 84484, 84485, 84487, 84507, 84509, 84528, 84539, 84545, 84549, 84550, 84555, 84560, 84568, 84596, 84628, 84634, 84635, 84641, 84654, 84694, 84708, 84713, 84721, 84722, 84725, 84741, 84745, 84750, 84768, 84788, 84803, 84828, 84838, 84839, 84840, 84850, 84853, 84858, 84867, 84869, 84880, 84892, 84893, 84904, 84918, 84939, 84954, 84956, 84973, 84978, 87026, 87040, 87068, 87076, 87121, 87196, 87245, 87255, 87259, (3) 41000, 41003, 41021, 41029, 41033, 41034, 41055, 41061, 41071, 41088, 41109, 41123, 41131, 41174, 41182, 41215, 41216, 41249, 41251, 41254, 41255, 41259, 41262, 41311, 41312, 41336, 41349, 41356, 41358, 41363, 41370, 41384, 41387, 41388, 41389, 41400, 41402, 41412, 41422, 41499, 41500, 41515, 41538, 41548, (4) 87655, (5) 61383, 61384, 61412, (6) 45601;

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Andorra, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, Colombia, C¿te D'Ivoire, Cyprus, Czech Republic, Denmark, Finland, France, French Guiana, Georgia, Germany, Greece, Guadeloupe, Hong Kong, Iceland, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kenya, Latvia, Lebanon, Libya, Lithuania, Malaysia, Malta, Martinique, Mexico, Moldova, Monaco, Netherlands, New Zealand, Norway, Palestine, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., Serbia, Slovenia, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, Ukraine, United Kingdom, U.A.E.

device · product 9 of 18

Product Name: Ingenia 1.5T S; Model Number: 781347;

Z-1796-2025
Recall number
Z-1796-2025
Initiated
May 13, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America Llc
Quantity
2 units (US Only)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Code information

Model Number: 781347; UDI-DI: 00884838068421; Serial Numbers: 81042, 81072;

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Andorra, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, Colombia, C¿te D'Ivoire, Cyprus, Czech Republic, Denmark, Finland, France, French Guiana, Georgia, Germany, Greece, Guadeloupe, Hong Kong, Iceland, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kenya, Latvia, Lebanon, Libya, Lithuania, Malaysia, Malta, Martinique, Mexico, Moldova, Monaco, Netherlands, New Zealand, Norway, Palestine, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., Serbia, Slovenia, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, Ukraine, United Kingdom, U.A.E.

device · product 10 of 18

Product Name: Ingenia 3.0T; Model Numbers: (1) 781342, (2) 781377, (3) 782103;

Z-1797-2025
Recall number
Z-1797-2025
Initiated
May 13, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America Llc
Quantity
193 units (36 US, 157 OUS)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Code information

Model Numbers: (1) 781342, (2) 781377, (3) 782103; UDI-DI: (1) 00884838055339, (2) 00884838009813, (3) 00884838098299; Serial Numbers: (1) 71029, 71031, 71038, 71185, 71193, 71319, 71322, 71336, 71355, 71532, 71556, 71739, 71796, 85006, 85066, 85154, 85191, 85201, 71001, 71002, 71006, 71008, 71026, 71051, 71061, 71072, 71088, 71095, 71101, 71154, 71163, 71164, 71184, 71214, 71231, 71269, 71288, 71309, 71311, 71313, 71335, 71341, 71344, 71347, 71366, 71374, 71384, 71385, 71412, 71413, 71420, 71427, 71438, 71441, 71442, 71445, 71446, 71448, 71450, 71453, 71459, 71462, 71463, 71475, 71484, 71486, 71489, 71493, 71521, 71558, 71562, 71564, 71565, 71574, 71589, 71590, 71597, 71604, 71611, 71615, 71616, 71619, 71620, 71639, 71641, 71647, 71673, 71684, 71686, 71704, 71715, 71723, 71725, 71733, 71737, 71749, 71756, 71759, 71773, 71780, 71806, 71813, 71816, 71831, 71841, 71849, 71850, 71862, 71882, 71885, 71889, 71921, 71923, 71925, 71954, 71979, 71986, 71992, 71993, 71994, 85015, 85038, 85045, 85068, 85076, 85078, 85085, 85087, 85091, 85125, 85126, 85148, 85150, 85180, 85183, 85216, 85276, 85319, 85377, 85391, (2) 42033, 42036, 42098, 42196, 42238, 42247, 42293, 42342, 42352, 42389, 42416, 42002, 42010, 42011, 42012, 42014, 42015, 42037, 42048, 42132, 42153, 42164, 42219, 42220, 42224, 42230, 42250, 42252, 42265, 42292, 42303, 42305, 42319, 42321, 42330, 42332, 42399, 42409, 42412, 42419, 42425, (3) 85652, 85653, 85654, 85679, 85683, 85701, 85714, 85601, 85604, 85606, 85686, 85723;

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Andorra, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, Colombia, C¿te D'Ivoire, Cyprus, Czech Republic, Denmark, Finland, France, French Guiana, Georgia, Germany, Greece, Guadeloupe, Hong Kong, Iceland, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kenya, Latvia, Lebanon, Libya, Lithuania, Malaysia, Malta, Martinique, Mexico, Moldova, Monaco, Netherlands, New Zealand, Norway, Palestine, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., Serbia, Slovenia, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, Ukraine, United Kingdom, U.A.E.

device · product 11 of 18

Product Name: Ingenia Ambition S; Model Numbers: (1) 781359, (2) 782108, (3) 782139;

Z-1798-2025
Recall number
Z-1798-2025
Initiated
May 13, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America Llc
Quantity
152 units (25 US, 127 OUS)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Code information

Model Numbers: (1) 781359, (2) 782108, (3) 782139; UDI-DI: (1) 00884838090057, (2) 00884838009813, (3) 00884838098299; Serial Numbers: (1) 48001, 48005, 48009, 48011, 48014, 48016, 48023, 48033, 48034, 48043, 48045, 48047, 48122, 48154, 48160, 48167, 48173, 48178, 48179, 48180, 48242, 48275, 48285, (2) 48501, 48503, 48507, 48524, 48530, 48537, 48548, 48549, 48557, 48564, 48566, 48568, 48569, 48571, 48576, 48577, 48580, 48582, 48588, 48589, 48591, 48595, 48607, 48608, 48612, 48614, 48620, 48628, 48638, 48641, 48666, 48667, 48668, 48669, 48671, 48672, 48673, 48686, 48688, 48692, 48694, 48695, 48696, 48697, 48698, 48718, 48721, 48726, 48749, 48778, 48818, 48819, 48831, 48847, 48854, 48878, 48888, 48895, 48907, (3) 29000, 29003, 29005, 29006, 29008, 29009, 29010, 29011, 29012, 29013, 29014, 29015, 29016, 29017, 29018, 29019, 29020, 29021, 29022, 29023, 29025, 29026, 29027, 29029, 29030, 29031, 29032, 29033, 29034, 29035, 29038, 29039, 29040, 29042, 29043, 29045, 29046, 29047, 29048, 29049, 29050, 29052, 29053, 29054, 29055, 29057, 29058, 29060, 29062, 29063, 29064, 29065, 29066, 29067, 29068, 29069, 29070, 29071, 29076, 29078, 29079, 29081, 29083, 29084, 29085, 29088, 29089, 29091, 29093, 29105;

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Andorra, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, Colombia, C¿te D'Ivoire, Cyprus, Czech Republic, Denmark, Finland, France, French Guiana, Georgia, Germany, Greece, Guadeloupe, Hong Kong, Iceland, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kenya, Latvia, Lebanon, Libya, Lithuania, Malaysia, Malta, Martinique, Mexico, Moldova, Monaco, Netherlands, New Zealand, Norway, Palestine, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., Serbia, Slovenia, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, Ukraine, United Kingdom, U.A.E.

device · product 12 of 18

Product Name: Ingenia 1.5T CX; Model Number: 781262;

Z-1799-2025
Recall number
Z-1799-2025
Initiated
May 13, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America Llc
Quantity
9 units (OUS Only)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Code information

Model Number: 781262; UDI-DI: 00884838068445; Serial Numbers: 77059, 77120, 77158, 77161, 77178, 77182, 77191, 77193, 77203;

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Andorra, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, Colombia, C¿te D'Ivoire, Cyprus, Czech Republic, Denmark, Finland, France, French Guiana, Georgia, Germany, Greece, Guadeloupe, Hong Kong, Iceland, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kenya, Latvia, Lebanon, Libya, Lithuania, Malaysia, Malta, Martinique, Mexico, Moldova, Monaco, Netherlands, New Zealand, Norway, Palestine, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., Serbia, Slovenia, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, Ukraine, United Kingdom, U.A.E.

device · product 13 of 18

Product Name: Ingenia 3.0T CX; Model Number: 781271;

Z-1800-2025
Recall number
Z-1800-2025
Initiated
May 13, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America Llc
Quantity
37 units (OUS Only)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Code information

Model Number: 781271; UDI-DI: 00884838068452; Serial Numbers: 78012, 78016, 78017, 78018, 78025, 78028, 78033, 78035, 78039, 78042, 78045, 78050, 78053, 78060, 78062, 78082, 78095, 78100, 78112, 78122, 78123, 78133, 78147, 78148, 78155, 78175, 78197, 78199, 78201, 78202, 78217, 78229, 78239, 78259, 78260, 78286, 78287;

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Andorra, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, Colombia, C¿te D'Ivoire, Cyprus, Czech Republic, Denmark, Finland, France, French Guiana, Georgia, Germany, Greece, Guadeloupe, Hong Kong, Iceland, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kenya, Latvia, Lebanon, Libya, Lithuania, Malaysia, Malta, Martinique, Mexico, Moldova, Monaco, Netherlands, New Zealand, Norway, Palestine, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., Serbia, Slovenia, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, Ukraine, United Kingdom, U.A.E.

device · product 14 of 18

Product Name: Ingenia Ambition X; Model Numbers: (1) 781356, (2) 782109, (3) 782138;

Z-1801-2025
Recall number
Z-1801-2025
Initiated
May 13, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America Llc
Quantity
300 units (81 US, 219 OUS)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Code information

Model Numbers: (1) 781356, (2) 782109, (3) 782138; UDI-DI: (1) 00884838090040, (2) 00884838098350, (3) 00884838108622; Serial Numbers: (1) 47002, 47004, 47011, 47012, 47018, 47019, 47020, 47028, 47029, 47037, 47049, 47052, 47057, 47099, 47173, 47184, 47187, 47189, 47200, 47203, 47204, 47206, 47211, 47215, 47222, 47230, 47231, 47242, 47245, 47252, 47258, 47260, 47268, 47270, 47274, 47281, 47283, 47286, 47290, 47294, 47297, 47301, 47304, 47309, 47312, 47313, 47314, 47328, 47342, 47347, 47351, (2) 47503, 47505, 47507, 47508, 47514, 47519, 47520, 47522, 47530, 47535, 47536, 47539, 47543, 47558, 47560, 47561, 47562, 47563, 47567, 47568, 47572, 47580, 47595, 47596, 47598, 47599, 47608, 47610, 47614, 47615, 47622, 47623, 47634, 47642, 47646, 47649, 47651, 47653, 47654, 47657, 47661, 47662, 47663, 47668, 47669, 47671, 47678, 47681, 47682, 47685, 47687, 47689, 47692, 47694, 47697, 47698, 47702, 47706, 47708, 47709, 47710, 47717, 47718, 47721, 47726, 47727, 47728, 47729, 47730, 47731, 47732, 47733, 47748, 47751, 47760, 47761, 47762, 47767, 47771, 47778, 47779, 47780, 47781, 47782, 47783, 47789, 47796, 47797, 47800, 47801, 47808, 47809, 47812, 47815, 47816, 47817, 47818, 47820, 47822, 47826, 47834, 47839, 47843, 47844, 47849, 47851, 47862, 47863, 47866, 47876, 47882, 47885, 47886, 47887, 47891, 47928, (3) 49000, 49001, 49002, 49003, 49004, 49008, 49009, 49010, 49013, 49014, 49015, 49017, 49019, 49020, 49021, 49025, 49026, 49027, 49029, 49031, 49033, 49034, 49036, 49043, 49044, 49045, 49047, 49048, 49049, 49052, 49053, 49054, 49056, 49057, 49058, 49060, 49062, 49063, 49064, 49066, 49067, 49068, 49069, 49070, 49071, 49072, 49073, 49075, 49076, 49077, 49078, 49079, 49080, 49081, 49086, 49087, 49088, 49089, 49090, 49091, 49092, 49093, 49094, 49095, 49096, 49097, 49098, 49099, 49100, 49101, 49102, 49103, 49104, 49105, 49106, 49107, 49108, 49109, 49110, 49111, 49113, 49114, 49115, 49116, 49117, 49118, 49119, 49121, 49124, 49128, 49129, 49130, 49131, 49134, 49136, 49140, 49144, 49145, 49146, 49147, 49148, 49152, 49153, 49154, 49155, 49156, 49157, 49158, 49160, 49161, 49162, 49163, 49164, 49165, 49166, 49168, 49171, 49172, 49178, 49179, 49180, 49181, 49182, 49183, 49186, 49197, 49203, 49205, 49212, 49217, 49226, 49227, 49231;

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Andorra, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, Colombia, C¿te D'Ivoire, Cyprus, Czech Republic, Denmark, Finland, France, French Guiana, Georgia, Germany, Greece, Guadeloupe, Hong Kong, Iceland, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kenya, Latvia, Lebanon, Libya, Lithuania, Malaysia, Malta, Martinique, Mexico, Moldova, Monaco, Netherlands, New Zealand, Norway, Palestine, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., Serbia, Slovenia, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, Ukraine, United Kingdom, U.A.E.

device · product 15 of 18

Product Name: Ingenia Elition S; Model Numbers: (1) 781357, (2) 782106, (3) 782137;

Z-1802-2025
Recall number
Z-1802-2025
Initiated
May 13, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America Llc
Quantity
65 units (6 US, 59 OUS)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Code information

Model Numbers: (1) 781357, (2) 782106, (3) 782137; UDI-DI: (1) 00884838088108, (2) 00884838098329, (3) 00884838108615; Serial Numbers: (1) 46002, 46004, 46007, 46012, 46013, 46015, 46016, 46018, 46020, 46021, 46023, 46025, 46039, 46049, 46054, 46068, 46076, 46082, 46085, 46092, 46101, (2) 46203, 46206, 46207, 46208, 46209, 46219, 46220, 46225, 46235, 46237, 46241, 46242, 46243, 46245, 46258, 46268, 46269, 46270, 46286, 46292, 46326, (3) 64001, 64002, 64003, 64004, 64005, 64007, 64008, 64009, 64011, 64013, 64014, 64015, 64016, 64019, 64022, 64023, 64024, 64028, 64029, 64030, 64032, 64034, 64045;

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Andorra, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, Colombia, C¿te D'Ivoire, Cyprus, Czech Republic, Denmark, Finland, France, French Guiana, Georgia, Germany, Greece, Guadeloupe, Hong Kong, Iceland, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kenya, Latvia, Lebanon, Libya, Lithuania, Malaysia, Malta, Martinique, Mexico, Moldova, Monaco, Netherlands, New Zealand, Norway, Palestine, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., Serbia, Slovenia, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, Ukraine, United Kingdom, U.A.E.

device · product 16 of 18

Product Name: Ingenia Elition X; Model Numbers: (1) 781358, (2) 782107, (3) 782136;

Z-1803-2025
Recall number
Z-1803-2025
Initiated
May 13, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America Llc
Quantity
198 units (25 US, 173 OUS)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Code information

Model Numbers: (1) 781358, (2) 782107, (3) 782136; UDI-DI: (1) 00884838088115, (2) 00884838098336, (3) 00884838108608; Serial Numbers: (1) 45010, 45023, 45028, 45029, 45032, 45033, 45034, 45037, 45040, 45041, 45043, 45045, 45046, 45048, 45049, 45053, 45066, 45070, 45072, 45076, 45087, 45090, 45091, 45092, 45093, 45102, 45105, 45108, 45115, 45116, 45119, 45127, 45136, 45138, 45140, 45144, 45147, 45154, 45156, 45157, 45162, 45168, 45181, 45184, 45189, 45191, 45194, 45205, 45222, 45227, 45231, 45243, 45244, 45245, 45246, 45250, 45252, 45263, 45272, 45277, 45278, 45289, 45290, 45296, 45317, 45319, 45323, 45328, 45333, 45335, 45340, 45342, 45362, 45374, 45379, 45414, (2) 45503, 45508, 45519, 45523, 45525, 45530, 45532, 45533, 45534, 45536, 45542, 45543, 45545, 45547, 45551, 45559, 45560, 45561, 45568, 45573, 45574, 45578, 45580, 45589, 45594, 62011, 62023, 62024, 62026, 62030, 62031, 62033, 62035, 62038, 62040, 62041, 62047, 62048, 62051, 62052, 62056, 62058, 62059, 62061, 62062, 62065, 62070, 62071, 62073, 62080, 62081, 62082, 62083, 62088, 62092, 62134, 62136, 62137, 62152, 62153, 62159, 62178, 62181, 62182, 62191, 62197, 62198, 62199, 62212, (3) 28500, 28502, 28503, 28504, 28506, 28507, 28509, 28510, 28514, 28515, 28516, 28517, 28518, 28520, 28521, 28523, 28524, 28525, 28526, 28527, 28528, 28529, 28531, 28532, 28533, 28535, 28536, 28537, 28538, 28539, 28540, 28542, 28543, 28545, 28546, 28547, 28548, 28550, 28552, 28554, 28555, 28559, 28560, 28561, 28563, 28564, 28565, 28566, 28568, 28569, 28572, 28575, 28581;

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Andorra, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, Colombia, C¿te D'Ivoire, Cyprus, Czech Republic, Denmark, Finland, France, French Guiana, Georgia, Germany, Greece, Guadeloupe, Hong Kong, Iceland, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kenya, Latvia, Lebanon, Libya, Lithuania, Malaysia, Malta, Martinique, Mexico, Moldova, Monaco, Netherlands, New Zealand, Norway, Palestine, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., Serbia, Slovenia, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, Ukraine, United Kingdom, U.A.E.

device · product 17 of 18

Product Name: MR 5300; Model Numbers: (1) 782110, (2) 782152;

Z-1804-2025
Recall number
Z-1804-2025
Initiated
May 13, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America Llc
Quantity
186 units (2 US, 184 OUS)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Code information

Model Numbers: (1) 782110, (2) 782152; UDI-DI: (1) 00884838099364, (2) 00884838112841; Serial Numbers: (1) 63007, 63011, 63022, 63043, 63047, 63050, 63051, 63060, 63074, 63078, 63079, 63082, 63085, 63090, 63095, 63097, 63100, 63116, 63121, 63132, 63136, 63137, 63142, 63143, 63144, 63146, 63150, 63156, 63160, 63162, 63166, 63190, 63202, 63210, 63222, 63226, 63228, 63235, 63238, 63239, 63244, 63247, 63258, 63262, 63263, 63264, 63265, 63266, 63267, 63268, 63269, 63270, 63272, 63274, 63275, 63276, 63281, 63282, 63283, 63284, 63285, 63286, 63287, 63288, 63289, 63290, 63292, 63300, 63303, 63304, 63305, 63306, 63307, 63337, 63352, 63356, 63361, 63363, 63366, 63367, 63370, 63372, 63394, 63456, 63596, 63599, (2) 69000, 69003, 69004, 69005, 69006, 69007, 69008, 69010, 69011, 69012, 69014, 69015, 69016, 69017, 69019, 69020, 69021, 69022, 69023, 69024, 69026, 69027, 69029, 69031, 69032, 69034, 69036, 69037, 69041, 69043, 69044, 69045, 69046, 69048, 69051, 69052, 69053, 69055, 69056, 69058, 69060, 69061, 69063, 69064, 69065, 69066, 69067, 69068, 69069, 69070, 69071, 69072, 69073, 69075, 69076, 69077, 69078, 69080, 69081, 69082, 69085, 69086, 69087, 69089, 69092, 69093, 69094, 69095, 69096, 69097, 69098, 69100, 69102, 69103, 69106, 69107, 69110, 69111, 69112, 69115, 69116, 69121, 69122, 69123, 69124, 69126, 69127, 69130, 69131, 69133, 69136, 69137, 69141, 69147, 69150, 69161, 69170, 69171, 69172, 69176;

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Andorra, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, Colombia, C¿te D'Ivoire, Cyprus, Czech Republic, Denmark, Finland, France, French Guiana, Georgia, Germany, Greece, Guadeloupe, Hong Kong, Iceland, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kenya, Latvia, Lebanon, Libya, Lithuania, Malaysia, Malta, Martinique, Mexico, Moldova, Monaco, Netherlands, New Zealand, Norway, Palestine, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., Serbia, Slovenia, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, Ukraine, United Kingdom, U.A.E.

device · product 18 of 18

Product Name: MR 7700; Model Numbers: (1) 782120, (2) 782153;

Z-1805-2025
Recall number
Z-1805-2025
Initiated
May 13, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Philips North America Llc
Quantity
72 units (6 US, 66 OUS)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.

Code information

Model Numbers: (1) 782120, (2) 782153; UDI-DI: (1) 00884838104112, (2) 00884838112858; Serial Numbers: (1) 65000, 65001, 65002, 65003, 65004, 65005, 65007, 65008, 65009, 65011, 65012, 65013, 65014, 65017, 65018, 65019, 65020, 65021, 65023, 65024, 65025, 65026, 65027, 65028, 65029, 65030, 65031, 65032, 65034, 65035, 65037, 65038, 65039, 65040, 65041, 65042, 65050, 65051, 65056, 65057, 65059, 65060, 65061, 65063, 65064, 65065, 65066, (2) 68000, 68001, 68006, 68007, 68008, 68009, 68010, 68011, 68012, 68013, 68014, 68015, 68016, 68017, 68018, 68020, 68023, 68024, 68025, 68028, 68029, 68030, 68031, 68034, 68037;

Distribution pattern

Worldwide distribution - US Nationwide and the countries of Andorra, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, Colombia, C¿te D'Ivoire, Cyprus, Czech Republic, Denmark, Finland, France, French Guiana, Georgia, Germany, Greece, Guadeloupe, Hong Kong, Iceland, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kenya, Latvia, Lebanon, Libya, Lithuania, Malaysia, Malta, Martinique, Mexico, Moldova, Monaco, Netherlands, New Zealand, Norway, Palestine, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., Serbia, Slovenia, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, Ukraine, United Kingdom, U.A.E.