FDA Medical devices recall ·
Allura Xper FD20 OR Table Product Codes: (1)722023, (2) 722035, (3) 722015 recall
- Recall number
- Z-2628-2025
- Date
- (initiated September 3, 2025)
- Company / brand
- Philips Medical Systems Nederland B.V.
Veenpluis 4-6, Best, N/A, Netherlands - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 174 units (45 US, 129 OUS)
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Allura Xper FD20 OR Table Product Codes: (1)722023, (2) 722035, (3) 722015; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;
Why was it recalled?
Systems may not perform as intended due to the deterioration of certain internal components (the CMOS battery, hard disk drive, and/or power supply unit). If this deterioration occurs, motorized movements of the system will become unavailable. Manual movements of the stand (longitudinal, transversal and rotational for ceiling mounted systems and rotational for floor mounted systems) and table longitudinal movements remain available. Imaging (X-ray) functionality remains available.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Product Codes: (1)722023, (2) 722035, (3) 722015; UDI-DI: (1) 00884838059085, (2) 00884838054240, (3) N/A; Serial numbers: (1) 27, 116, 12, 175, 98, 35, 142, 179, 46, 64, 110, 124, 66, 117, 109, 42, 138, 82, 83, 127, 75, 118, 41, 121, 70, 119, 112, 25, 159, 137, 47, 173, 114, 167, 164, 4, 16, 14, 107, 9, 13, 105, 5, 132, 2, 21, 38, 102, 52, 84, 56, 150, 144, 149, 134, 60, 15, 68, 126, 79, 145, 123, 135, 157, 32, 53, 152, 108, 95, 34, 87, 94, 57, 58, 165, 86, 125, 103, 3, 31, (2) 123, 38, 85, 101, 117, 21, 57, 145, 119, 100, 47, 127, 52, 131, 124, 89, 46, 74, 59, 121, 34, 72, 111, 128, 84, 10, 11, 40, 108, 144, 266, 80, 113, 130, 122, 109, 96, 53, 58, 104, 56, 69, 71, 75, 76, 208, 110, 149, 49, 105, 82, 136, 15, 146, 48, 16, 95, 64, 17, 106, 81, 29, 116, 102, 13, 12, 32, 35, 62, 107, 142, 43, 77, 94, 33, 37, 61, 51, 50, 19, 28, 97, 148, 114, 3, 151, 79, 129, 65, 25, 26, 103, 98, (3) 3;
Distribution
Worldwide distribution - US Nationwide and the countries of Albania, Algeria, Argentina, Australia, Austria, Azerbaijan, Bangladesh, Belarus, Belgium, Brazil, Bulgaria, Canada, Chile, China, Colombia, Costa Rica, Cuba, Cyprus, Czech Republic, Denmark, Dominican Rep, Ecuador, Egypt, Estonia, Fiji, Finland, France, FrenchPolynesia, Georgia, Germany, Greece, Honduras, Hong Kong, Hungary, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kenya, Kosovo, Lao, Lebanon, Libya, Lithuania, Macedonia, Malaysia, Malta, Martinique, Mauritius, Mexico, Mongolia, Morocco, Myanmar, Nepal, Netherlands, New Caledonia, New Zealand, Norway, Oman, Pakistan, Palestine, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Qatar, R¿union, Romania, Russian Fed., Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Africa, South Korea, Spain, Sri Lanka, Sudan, Sweden, Switzerland, Syria, Taiwan, Tanzania, Thailand, Tunisia, T¿rkiye, Ukraine, United Kingdom, Uruguay, Utd.Arab.Emir., Uzbekistan, Venezuela, Vietnam, Yemen.
States: Georgia
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-2628-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.