FDA Medical devices recall ·
Philips Zenition 70, Model Number: 718133 recall
- Recall number
- Z-0353-2025
- Date
- (initiated October 7, 2024)
- 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
- 2,247 units (582 US, 84 Canada, 1,581 R.O.W.)
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Philips Zenition 70, Model Number: 718133
Why was it recalled?
Potential for the Mains Control Unit board fuse may blow out during system start-up or during a procedure.
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
Model Number: 718133; UDI-DI: (01)00884838091528(21); Serial Numbers: 420, 4093, 2851, 3947, 2571, 4211, 3325, 3326, 2324, 3665, 491, 480, 579, 580, 581, 582, 4138, 71, 3657, 3660, 3889, 669, 670, 671, 233, 3416, 4351, 4352, 4353, 4355, 3971, 3972, 4387, 4278, 2880, 3366, 4062, 4063, 3374, 4201, 4083, 1290, 3894, 932, 933, 4309, 1796, 3355, 3680, 4156, 562, 1983, 4206, 3395, 1310, 3758, 63, 1787, 2888, 684, 235, 557, 4014, 2056, 3658, 3661, 1801, 108, 109, 3354, 572, 1901, 4431, 1086, 1868, 1899, 1758, 2081, 4223, 626, 652, 654, 655, 829, 1786, 2957, 3800, 1904, 3393, 4155, 4302, 3523, 4170, 4432, 651, 85, 4013, 3973, 1902, 563, 2202, 1903, 4386, 234, 2720, 202, 553, 3686, 822, 672, 3631, 72, 3892, 3893, 3895, 3896, 4176, 3491, 2958, 1219, 3392, 653, 1195, 1900, 4147, 2938, 1072, 101, 103, 2106, 1569, 3394, 1848, 1852, 4020, 4186, 3604, 106, 4096, 561, 1802, 4094, 3348, 1837, 944, 1192, 1625, 1194, 4396, 4279, 4280, 3683, 1944, 3940, 2887, 1204, 62, 1536, 1212, 20, 52, 1675, 2380, 2381, 2681, 2276, 2342, 1525, 1224, 2105, 3385, 3459, 1581, 2680, 4111, 2172, 3583, 1599, 1945, 4252, 1451, 4167, 4171, 3133, 3135, 3585, 3933, 3623, 1619, 1621, 29, 3582, 2549, 3048, 2203, 3560, 2721, 435, 474, 49, 3741, 1422, 1423, 1, 10, 11, 12, 13, 2, 3, 4, 5, 6, 7, 8, 9, 1143, 2715, 2804, 1839, 3118, 1196, 50, 4570, 2705, 32, 1376, 1377, 1379, 1381, 2747, 65, 3313, 66, 68, 69, 70, 512, 796, 1919, 2639, 2155, 2156, 1922, 1095, 1096, 2323, 3496, 3497, 3870, 1288, 2570, 311, 3387, 3682, 4035, 4036
Distribution
Worldwide distribution - US Nationwide and the countries of Albania, Algeria, Argentina, Australia, Austria, Bahrain, Bangladesh, Belgium, Bolivia, Brazil, Bulgaria, Chile, China, Colombia, Croatia, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, El Salvador, Estonia, Faroe Islands, Fiji, Finland, France, French Guiana, Germany, Gibraltar, Greece, Guatemala, Hong Kong, Hungary, Iceland, India, Indonesia, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kenya, Korea, Republic of, Kuwait, Lao People's Democratic Republic, Lebanon, Lithuania, Malaysia, Malta, Martinique, Mauritius, Mexico, Morocco, Myanmar, Netherlands, New Zealand, Nicaragua, Nigeria, Norway, Pakistan, Palestine, State of, Panama, Peru, Philippines, Poland, Portugal, R¿union, Romania, Russian Federation, Rwanda, Saudi Arabia, Serbia, Singapore, Slovakia, South Africa, Spain, Suriname, Sweden, Switzerland, Taiwan, Thailand, Trinidad and Tobago, Turkey, Ukraine, United Arab Emirates, United Kingdom, Uzbekistan, Viet Nam, Yemen.
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-0353-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.