Skip to content
RecallWatchMedical Device Safety
Class IIOngoingZ-0466-2026

Philips Medical Systems DMC GmbH recalls Radiography 7300 C

Philips Medical Systems DMC GmbHHamburg, GermanyReported Nov 19, 2025 · 8 months ago
Legal News Analyst ·

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.

Affected product

Check your device

Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.

Radiography 7300 C; Model Number: 712037;

Lot / code information

Model
712037
UDI
00884838116016
Serial #
6, 7, 8, 9, 11, 12 — +278 moreShow all
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

What the firm is doing

On October 1, 2025, "URGENT MEDICAL DEVICE CORRECTION" letters dated September 30, 2025, were sent to customers. The letters described the problem, product and actions to be taken. Actions to be taken: It is safe to continue to use the system(s) in accordance with the intended use. It is recommended that customers use the motorized movement option until the technical solution has been implemented. The system may experience motor drive errors if the force for movement exceeds 110N, which restricts the motorized movement. If the motorized movement does not function, customers should contact their local service representative. B. Circulate this notice to all users of this device so that they are aware of the issue and associated hazard/harm. C. Please retain this Urgent Medical Device Correction letter with your system(s) until the solution is installed; ensure the notice is in a place likely to be seen/viewed. 5. Actions planned by Philips to correct the problem. Philips will provide the technical solution details when finalized. This notice has been reported to the appropriate Regulatory Agencies. If you need any further information or support concerning this issue, please contact your local Philips representative. For North America, contact the Customer Care Solutions Center (1-800-722-9377, 8AM 8PM EST, Monday-Friday).

DistributionShow details

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.,

Class IIWhat this means

Use of the product may cause temporary or medically reversible adverse health consequences.

Sources & references

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.

Taylor Coteus
Legal News Analyst

Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.

More Class II recalls