Philips Medical Systems North America Co. Phillips Philips BV Endura R2.2 Mobile X-ray system. The Type Product Code 718074 can be found under the X-ray trolley cover on the front lower right side of the module or under the stand cover. The device brochure is labeled in part: "Philips...Mobile C-Arm system BV Endura". Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Philips BV Endura R2.2 Mobile X-ray system. The Type Product Code 718074 can be found under the X-ray trolley cover on the front lower right side of the module or under the stand cover. The device brochure is labeled in part: "Philips...Mobile C-Arm system BV Endura".
Brand
Philips Medical Systems North America Co. Phillips
Lot Codes / Batch Numbers
127 units are identified with Site Numbers: 544982, 546114, 546792, 546793, 547164, 548598, 548686, 548983, 549986, 549987, 550126, 550127, 550281, 550409, 550838, 550959, 551127, 551274, 551492, 551525, 551589, 551695, 551730, 552376, 552393, 552394, 552398, 552444, 552467, 552468, 552669, 552990, 553098, 553171, 553271, 553860, 553917, 553976, 553989, 554350, 554363, 554497, 554507, 554658, 554779, 555001, 555021, 555243, 555395, 555463, 555517, 555821, 556135, 556171, 556192, 556202, 556215, 556531, 556587, 556608, 556612, 556678, 556862, 556947, 556977, 556979, 557037, 557063, 557147, 557510, 557520, 557590, 558233, 558237, 558613, 558868, 558975, 559070, 559663, 559665, 41416327, 41443832, 41443860, 41445126, 41445430, 41445445, 41445552, 41445931, 41446303, 41566246, 41585083, 41630870, 41658558, 41661638, 41765654, 41796621, 41905206, 41938039, 41955473, 41957114, 42045315, 42162893, 42291865, 42326711, 42373518, 42382482, 42394051, 42472756, 42551956, 42608281, 42639034, 42824768, 42861875, 42869100, 42880805, 42966787, 43181969, 43209307, 43209310, 43341471, 43453560, 43618928, 43618930, 43721228, 43722015, 45050110, and 45149708.
Products Sold
127 units are identified with Site Numbers: 544982, 546114, 546792, 546793, 547164, 548598, 548686, 548983, 549986, 549987, 550126, 550127, 550281, 550409, 550838, 550959, 551127, 551274, 551492, 551525, 551589, 551695, 551730, 552376, 552393, 552394, 552398, 552444, 552467, 552468, 552669, 552990, 553098, 553171, 553271, 553860, 553917, 553976, 553989, 554350, 554363, 554497, 554507, 554658, 554779, 555001, 555021, 555243, 555395, 555463, 555517, 555821, 556135, 556171, 556192, 556202, 556215, 556531, 556587, 556608, 556612, 556678, 556862, 556947, 556977, 556979, 557037, 557063, 557147, 557510, 557520, 557590, 558233, 558237, 558613, 558868, 558975, 559070, 559663, 559665, 41416327, 41443832, 41443860, 41445126, 41445430, 41445445, 41445552, 41445931, 41446303, 41566246, 41585083, 41630870, 41658558, 41661638, 41765654, 41796621, 41905206, 41938039, 41955473, 41957114, 42045315, 42162893, 42291865, 42326711, 42373518, 42382482, 42394051, 42472756, 42551956, 42608281, 42639034, 42824768, 42861875, 42869100, 42880805, 42966787, 43181969, 43209307, 43209310, 43341471, 43453560, 43618928, 43618930, 43721228, 43722015, 45050110, and 45149708.
Philips Medical Systems North America Co. Phillips is recalling Philips BV Endura R2.2 Mobile X-ray system. The Type Product Code 718074 can be found under the X-r due to Reliability of the Stand-Trolley cable may result in loss of images on the monitor during an examination. This intermittent problem can lead to System. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Reliability of the Stand-Trolley cable may result in loss of images on the monitor during an examination. This intermittent problem can lead to System lock-up, where no radiation is possible and images are not visible on the monitor
Recommended Action
Per FDA guidance
On 10/04/2008, Philips began sending the URGENT-Device Correction BV Pulsera R2.2 and Endura R2.2 letters to their customers. On 09/03/2008, the firm issued the Field Change Order (FCO) 71800024 and the firm's representative will replace the stand-trolley cable free of charge. Customers should contact Philips Call Center at 1-800-722-9377, #5, #2, and reference "FCO 71800024" with any questions.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026