Philips Medical Systems DMC GmbH recalls Radiography 7300 C

Recalling company

Philips Medical Systems DMC GmbH

Product

Radiography 7300 C; Model Number: 712037;

Reason

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.

Classification

Class II – may cause temporary or medically reversible health consequences

Recall date

Oct 1, 2025

Reported

Nov 19, 2025

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.,

Status

Ongoing

Quantity

284 units

Lot / codes

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, 24

Company location

Hamburg

Recall type

Voluntary: Firm initiated

Recall number

Z-0466-2026

Agency

U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-0466-2026 in the FDA Enforcement Report. Also see FDA recall press releases.