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Lower risk Medical device recall · FDA · Published October 1, 2025

Philips Radiography 7300 C Model 712037 May Require Extra Effort to Move Vertically

Philips recalls Radiography 7300 C models from July 2024 to June 2025 that may require extra force to move vertically due to manufacturing issues. Affected units have specific serial numbers and model numbers.

🇺🇸 FDA recall #Z-0466-2026Medical devicePhilips ›
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Recalling firmPhilips Medical Systems DMC GmbHDevelopment And Manufacturing Ctr., Rontgenstr. 24 · Hamburg, Germany
✎ GovInfoNow plain-language explainer

Philips is recalling certain Radiography 7300 C models (model number 712037) produced between July 2024 and June 2025 because some ceiling suspension telescopic carriages may be difficult to move vertically. This could cause extra physical effort for users during operation. Read more at govinfonow.com/recall/51120-philips-radiography-7300-c-model-712037-may-require-extra-effort.

Source Summary by GovInfoNow · govinfonow.com/recall/51120-philips-radiography-7300-c-model-712037-may-require-extra-effort · Updated August 18, 2026 · FDA enforcement record: FDA #Z-0466-2026

Cite this page

“Philips Radiography 7300 C Model 712037 May Require Extra Effort to Move Vertically.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/51120-philips-radiography-7300-c-model-712037-may-require-extra-effort. Based on FDA recall #Z-0466-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0466-2026%22&limit=1).

The FDA announced on Oct. 1, 2025, that Philips Medical Systems DMC GmbH is recalling Radiography 7300 C units due to potential manufacturing issues. The ceiling suspension telescopic carriages may be difficult to move vertically because additional force is required for manual movement.

How to tell if you have it

  • Brand: Philips
  • Product: Radiography 7300 C
  • Model Number: 712037
  • UDI-DI: 00884838116016
  • Serial Numbers: 6, 7, 8, 9, 11, 12, 13, 14, 15, 17, 24860004 through 24860126 (excluding listed gaps), 24860128 through 24860131, 24860133, 24860135, 24860137, 24860139 through 24860146, 24860148, 24860149, 24860150, 24860153, 24860157 through 24860159, 24860163 through 24860170, 24860172 through 24860187, 24860191, 24860192, 24860193, 24860196 through 24860200, 24860203 through 24860205, 24860207 through 24860214, 24860216 through 24860229, 24860232 through 24860241, 24860248, 24860252, 24860254 through 24860257, 24860259, 24860260, 24860261, 24860262, 24860264 through 24860273, 24860275 through 24860278, 24860280 through 24860284, 24860286, 24860288, 24860289, 24860290, 24860294 through 24860299, 24860302, 24860306, 24860308, 24860310 through 24860312, 24860314, 24860315, 24860317 through 24860319, 24860321, 24860322, 24860324, 24860325, 24860328, 24860332, 24860337 through 24860340, 24860342 through 24860344, 24860352, 24860355 through 24860357, 24860361, 24860363, 24860365 through 24860370, 24860372, 24860373, 24860376, 24860382 through 24860384, 24860388, 24860390 through 24860394, 24860401, 24860404, 24860407, 24860410, 24860411, 24860416, 24860420, 24860425
  • Manufacture Date: July 2024 through June 2025

The hazard

The FDA said the ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically. This issue requires additional force or physical exertion for manual movement due to potential manufacturing issues.

Context

GovInfoNow's records show Philips Medical Systems DMC GmbH has 1 other recall on record since 2021-05-19, including a 2021-05-19 notice for the Philips DigitalDiagnost C90 regarding incorrect radiation dose risk. Other recent recalls of similar products include Siemens ARTIS icono ceiling (2026-05-20), Siemens ARTIS Icono Biplane (2026-05-20), and Canon Alphenix INFX-8000C X-ray System (2025-12-19).

How to tell if you have this one

Check if your Radiography 7300 C has model number 712037 and serial numbers listed in the recall (e.g., 24860004, 24860006, etc.). The units were manufactured from July 2024 through June 2025.

  • Brand
    Philips
  • Category
    Medical device
FDA recall event · 6 products

All 6 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Ongoing
  • Distribution
    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.,
Recall numberProduct, codes & lotsQuantity
Z-0461-2026ProxiDiagnost N90; Model Number: 706110;; Model Number: 706110; UDI-DI: 00884838103221; Serial Number: 10001185, 10001205, 10001220, 10001224, 10001225, 10001227, 10001228, 10001229, 10001230, 10001231, 10001234, 10001235, 10001236, 10001237, 10001239, 10001245, 10001247, 10001248, 10001249, 10001250, 10001251, 10001253, 10001256, 10001257, 10001258, 10001261, 10001262, 10001264, 10001265, 10001266, 10001269, 10001270, 10001271, 10001272, 10001273, 10001274, 10001275, 10001276, 10001277, 10001278, 10001282;41 units
Z-0462-2026CombiDiagnost R90; Model Number: 709031;; Model Number: 709031; UDI-DI: 00884838101456; Serial Number: 100001385, 100001402, 100001409, 100001412, 100001415, 100001416, 100001417, 100001424, 100001426, 100001432, 100001449, 100001460, 100001464, 100001476, 100001480, 100001483, 100001488;17 units
Z-0463-2026Precision CRF; Model Number: 706400;; Model Number: 706400; UDI-DI: 00884838110588; Serial Number: 19, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 10001178, 10001179, 10001181, 10001182, 10001184, 10001185, 10001186, 10001187, 10001188, 10001189, 10001190, 10001191, 10001192, 10001193, 10001194, 10001195, 10001196, 10001197, 10001199, 10001200, 10001201, 10001202, 10001203, 10001204, 10001205, 10001206, 10001208, 10001209;42 units
Z-0464-2026DigitalDiagnost 4 (1) High Performance, (2) Flex/Value; Model Number: (1) 712031, (2) 712032;; 1. Model Number: 712031; UDI-DI: 00884838065321; Serial Numbers: 10001181, 10001182, 10001185, 10001186, 10001188, 10001189, SN16000022, SN20000013; 2. Model Number: 712032; UDI-DI: 00884838074514; Serial Numbers: 10001179, 19000341, 19000342, 19000343;12 units
Z-0465-2026DigitalDiagnost C90 (1) High Performance, (2) Flex/Value/Chest/ER; Model Number: (1) 712034, (2) 712035;; 1. Model Number: 712034; UDI-DI: 00884838090699; Serial Numbers: 22860392, 22860404, 22860437, 22860556, 22860559, 22860578, 22860581, 22860583, 22860584, 23860409, 23860424, 23860428, 23860607, 23860625, 23860632, 23860652, 23860656, 23860658, 23860665, 23860667, 23860668, 23860669, 23860680, 23860684, 23860693, 23860700, 23860717, 23860769, 23860780, 23860812, 23860820, 23860823, 23860824, 24860041, 24860042, 24860043, 24861002, 24861010, 24861018, 24861020, 24861021, 24861031, 24861036, 24861039, 24861040, 24861041, 24861042, 24861055, 24861063, 24861072, 24861076, 24861083, 24861086, 24861088, 24861091, 24861105, 24861106, 24861107, 24861108, 24861110, 24861112, 24861114, 24861118, 24861121, 24861123, 24861124, 24861125, 24861126, 24861128, 24861130, 24861132, 24861133, 24861135, 24861136, 24861137, 24861138, 24861140, 24861141, 24861142, 24861143, 24861150, 24861153, 24861155, 24861160, 24861162, 24861165, 24861175, 24861203, 24861206, 24861207, 24861208, 24861216, 24861225, 24861226, 24861233, 24861234, 24861237, 24861238, 24861239, 24861240, 24861241, 24861242, 24861243, 24861245, 24861254, 24861255, 24861256, 24861257, 24861258, 24861259, 24861261, 24861262, 24861263, 24861264, 24861265, 24861268, 24861269, 24861271, 24861285, 24861286, 24861290, 24861291, 24861294, 24861295, 24861297, 24861298, 24861299, 24861300, 24861301, 24861305, 24861308, 24861314, 24861317, 24861318, 24861319, 24861320, 24861321, 24861324, 24861326, 24861327, 24861328, 24861329, 24861331, 24861340, 24861341, 24861342, 24861343, 24861344, 24861346, 24861352, 24861360, 24861361, 24861362, 24861363, 24861364, 24861365, 24861366, 24861367, 24861369, 24861370, 24861372, 24861373, 24861378, 24861381, 24861382, 24861385, 24861386, 24861387, 24861388, 24861389, 24861391, 24861397, 24861398, 24861399, 24861400, 24861401, 24861404, 24861405, 24861407, 24861408, 24861410, 24861411, 24861412, 24861413, 24861414, 24861418, 24861419, 24861420, 24861421, 24861423, 24861424, 24861428, 24861429, 24861435, 24861436, 24861438, 24861439, 24861440, 24861441, 24861442, 24861443, 24861446, 24861450, 24861451, 24861455, 24861456, 24861459, 24861460, 22860131; 2. Model Number: 712035; UDI-DI: 00884838090705; Serial Numbers: 23860438, 24861021, 24861023, 24861037, 24861044, 24861045, 24861046, 24861047, 24861054, 24861055, 24861061, 24861062, 24861063, 24861064;223 units
Z-0466-2026Radiography 7300 C; Model Number: 712037;; 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;284 units
Based on the official FDA remedy

What to do — step by step

  1. Check Model Number

    Verify your Radiography 7300 C has model number 712037 and a serial number from the list provided in the recall.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “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,…” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA published this recall 49 days after the firm started it.

1. Firm started the recall: Oct 1, 202512. FDA classified it Class II: Nov 7, 202523. Published in FDA’s Enforcement Report: Nov 19, 202532025
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-0466-2026 (October 1, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0466-2026 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA