CLASS II ONGOING Device recall · Reported 19 Nov 2025 · FDA Enforcement Report

Radiography 7300 C recalled by Philips Medical Systems DMC

Philips Medical Systems DMC is recalling Radiography 7300 C, distributed nationwide in the US. The recall was initiated on 1 Oct 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesModel Number: 712037; UDI-DI: 00884838116016; Serial Numbers: 6, 7, 8, 9, 11, 12, 13, 14, 15, 17, 24860004, 24860006, 24860008, 24860009, 24860010, 24860011, 24860012, 24860013, 24860014, 24860015, 24860017, 24860018, 24860019, 24860021, 24860034, 24860036, 24860037, 24860038, 24860039, 24860040, 24860044, 24860045, 24860047, 24860049, 24860051, 24860053, 24860055, 24860056, 24860057, 24860058, 24860059, 24860060, 24860061, 24860062, 24860064, 24860065, 24860066, 24860067, 24860068, 24860069, 24860070, 24860072, 24860073, 24860074, 24860075, 24860076, 24860077, 24860078, 24860079, 24860080, 24860081, 24860082, 24860083, 24860084, 24860085, 24860086, 24860087, 24860088, 24860089, 24860090, 24860091, 24860092, 24860093, 24860094, 24860096, 24860098, 24860099, 24860100, 24860101, 24860102, 24860103, 24860104, 24860105, 24860106, 24860107, 24860108, 24860109, 24860110, 24860111, 24860112, 24860113, 24860115, 24860116, 24860117, 24860118, 24860119, 24860120, 24860121, 24860122, 24860123, 24860124, 24860125, 24860126, 24860128, 24860129, 24860130, 24860131, 24860133, 24860135, 24860137, 24860139, 24860141, 24860142, 24860143, 24860144, 24860145, 24860146, 24860148, 24860149, 24860150, 24860153, 24860157, 24860158, 24860159, 24860163, 24860164, 24860165, 24860166, 24860167, 24860168, 24860169, 24860170, 24860172, 24860173, 24860174, 24860175, 24860177, 24860178, 24860179, 24860180, 24860181, 24860182, 24860183, 24860184, 24860185, 24860186, 24860187, 24860191, 24860192, 24860193, 24860196, 24860197, 24860198, 24860200, 24860203, 24860204, 24860205, 24860207, 24860208, 24860209, 24860210, 24860211, 24860212, 24860213, 24860214, 24860216, 24860217, 24860218, 24860219, 24860220, 24860221, 24860222, 24860223, 24860224, 24860225, 24860226, 24860227, 24860228, 24860229, 24860232, 24860233, 24860234, 24860235, 24860236, 24860237, 24860238, 24860239, 24860240, 24860241, 24860248, 24860252, 24860254, 24860255, 24860256, 24860257, 24860259, 24860260, 24860261, 24860262, 24860264, 24860265, 24860266, 24860267, 24860268, 24860269, 24860270, 24860271, 24860272, 24860273, 24860275, 24860276, 24860277, 24860278, 24860280, 24860281, 24860282, 24860283, 24860284, 24860286, 24860288, 24860289, 24860290, 24860294, 24860295, 24860296, 24860297, 24860298, 24860299, 24860302, 24860306, 24860308, 24860310, 24860311, 24860312, 24860314, 24860315, 24860317, 24860318, 24860319, 24860321, 24860322, 24860324, 24860325, 24860328, 24860332, 24860337, 24860338, 24860339, 24860340, 24860342, 24860343, 24860344, 24860352, 24860355, 24860356, 24860357, 24860361, 24860363, 24860365, 24860366, 24860367, 24860368, 24860369, 24860370, 24860372, 24860373, 24860376, 24860382, 24860383, 24860384, 24860388, 24860390, 24860391, 24860392, 24860393, 24860394, 24860401, 24860404, 24860407, 24860410, 24860411, 24860416, 24860420, 24860425;

Quantity recalled284 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-0466-2026
FDA event ID: 97748
Recalling firm: Philips Medical Systems DMC, Hamburg
Classification: Class II
Status: Ongoing
Recall initiated: 1 Oct 2025
FDA classified: 7 Nov 2025
Reported: 19 Nov 2025
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Device type: Imaging Equipment

Timeline

1 Oct 2025	Recall initiated by company
7 Nov 2025	Classified by FDA	+37 days
19 Nov 2025	Published in enforcement report	+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues.

Product as listed by the FDA

Radiography 7300 C; Model Number: 712037;

Where it was distributed

Worldwide Distribution: US (Nationwide) Distribution and OUS (International) countries of: Australia, Austria, Bahrain, Belgium, Bosnia-Herz., Canada, Chile, Croatia, Denmark, Estonia, Finland, France, Germany, Ghana, Gibraltar, Guadeloupe, Indonesia, Iraq, Israel, Italy, Jordan, Kuwait, Kyrgyzstan, Latvia, Lithuania, Netherlands, New Zealand, Norway, Panama, Philippines, Poland, Portugal, R¿union, Samoa, Saudi Arabia, Singapore, South Africa, South Korea, Spain, Sweden, Switzerland, T¿rkiye, Turkmenistan, United Kingdom, Utd.Arab.Emir.,

Nationwide

Questions about this recall

Is Radiography 7300 C recalled?

Yes. Philips Medical Systems DMC recalled Radiography 7300 C on 1 Oct 2025. The recall is Class II and its status is Ongoing. Recall number Z-0466-2026.

Why was it recalled?

Which lots are affected?

Model Number: 712037; UDI-DI: 00884838116016; Serial Numbers: 6, 7, 8, 9, 11, 12, 13, 14, 15, 17, 24860004, 24860006, 24860008, 24860009, 24860010, 24860011, 24860012, 24860013, 24860014, 24860015, 24860017, 24860018, 24860019, 24860021, 24860034, 24860036, 24860037, 24860038, 24860039, 24860040, 24860044, 24860045, 24860047, 24860049, 24860051, 24860053, 24860055, 24860056, 24860057, 24860058, 24860059, 24860060, 24860061, 24860062, 24860064, 24860065, 24860066, 24860067, 24860068, 24860069, 24860070, 24860072, 24860073, 24860074, 24860075, 24860076, 24860077, 24860078, 24860079, 24860080, 24860081, 24860082, 24860083, 24860084, 24860085, 24860086, 24860087, 24860088, 24860089, 24860090, 24860091, 24860092, 24860093, 24860094, 24860096, 24860098, 24860099, 24860100, 24860101, 24860102, 24860103, 24860104, 24860105, 24860106, 24860107, 24860108, 24860109, 24860110, 24860111, 24860112, 24860113, 24860115, 24860116, 24860117, 24860118, 24860119, 24860120, 24860121, 24860122, 24860123, 24860124, 24860125, 24860126, 24860128, 24860129, 24860130, 24860131, 24860133, 24860135, 24860137, 24860139, 24860141, 24860142, 24860143, 24860144, 24860145, 24860146, 24860148, 24860149, 24860150, 24860153, 24860157, 24860158, 24860159, 24860163, 24860164, 24860165, 24860166, 24860167, 24860168, 24860169, 24860170, 24860172, 24860173, 24860174, 24860175, 24860177, 24860178, 24860179, 24860180, 24860181, 24860182, 24860183, 24860184, 24860185, 24860186, 24860187, 24860191, 24860192, 24860193, 24860196, 24860197, 24860198, 24860200, 24860203, 24860204, 24860205, 24860207, 24860208, 24860209, 24860210, 24860211, 24860212, 24860213, 24860214, 24860216, 24860217, 24860218, 24860219, 24860220, 24860221, 24860222, 24860223, 24860224, 24860225, 24860226, 24860227, 24860228, 24860229, 24860232, 24860233, 24860234, 24860235, 24860236, 24860237, 24860238, 24860239, 24860240, 24860241, 24860248, 24860252, 24860254, 24860255, 24860256, 24860257, 24860259, 24860260, 24860261, 24860262, 24860264, 24860265, 24860266, 24860267, 24860268, 24860269, 24860270, 24860271, 24860272, 24860273, 24860275, 24860276, 24860277, 24860278, 24860280, 24860281, 24860282, 24860283, 24860284, 24860286, 24860288, 24860289, 24860290, 24860294, 24860295, 24860296, 24860297, 24860298, 24860299, 24860302, 24860306, 24860308, 24860310, 24860311, 24860312, 24860314, 24860315, 24860317, 24860318, 24860319, 24860321, 24860322, 24860324, 24860325, 24860328, 24860332, 24860337, 24860338, 24860339, 24860340, 24860342, 24860343, 24860344, 24860352, 24860355, 24860356, 24860357, 24860361, 24860363, 24860365, 24860366, 24860367, 24860368, 24860369, 24860370, 24860372, 24860373, 24860376, 24860382, 24860383, 24860384, 24860388, 24860390, 24860391, 24860392, 24860393, 24860394, 24860401, 24860404, 24860407, 24860410, 24860411, 24860416, 24860420, 24860425;

Where was it sold?

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from Philips Medical Systems DMC

All 11

Reported	Class	Recall	Company	Reason	Where
19 Nov 2025Device	CLASS II	DigitalDiagnost 4 High Performance, Flex/Value recalled	Philips Medical Systems DMC	Other	Nationwide
19 Nov 2025Device	CLASS II	CombiDiagnost R90 recalled by Philips Medical Systems DMC	Philips Medical Systems DMC	Other	Nationwide
19 Nov 2025Device	CLASS II	ProxiDiagnost N90 recalled by Philips Medical Systems DMC	Philips Medical Systems DMC	Other	Nationwide
19 Nov 2025Device	CLASS II	Precision CRF recalled by Philips Medical Systems DMC	Philips Medical Systems DMC	Other	Nationwide
19 Nov 2025Device	CLASS II	DigitalDiagnost C90 High Performance, Flex/Value/Chest/ER recalled	Philips Medical Systems DMC	Other	Nationwide

Other Imaging Equipment recalls

All 2,336

Reported	Class	Recall	Company	Reason	Where
9 Sep 2026Device	CLASS II	Medline Convenience Kits containing BD ChloraPrep Clear recalled	Medline Industries	Lead & Heavy Metals	Nationwide
9 Sep 2026Device	CLASS II	Medline Convenience Kits: Ultrasound Breast Pack recalled	Medline Industries	Sterility	Nationwide
2 Sep 2026Device	CLASS II	Alphenix Models Infx-8000C Infx-8000F Infx-8000V This device is recalled	Canon Medical System, USA	Other	Nationwide
2 Sep 2026Device	CLASS II	Merge PACS and Merge OrthoPACS recalled by Merge Healthcare	Merge Healthcare	Labeling Errors	Nationwide
19 Aug 2026Device	CLASS II	Philips Azurion recalled by Philips Medical Systems	Philips Medical Systems Nederland B.v	Lead & Heavy Metals