Philips Azurion Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of…
Medical device recall Z-1152-2024. Published in FDA’s Enforcement Report on Feb 28, 2024.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Feb 28, 2024. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Ongoing its status, in FDA’s file
- Nationwide FDA’s word, and 49 states named
- 13, 133 (3,408 US; 9,725 ROW) how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
Disk Bay may not perform as intended. System may stop functioning and imaging may not be possible, resulting in delay of procedure.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Philips Azurion Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of the affected system. Affected PCs: XRay PC, Suite PC, and FlexViewing PC Azurion Model Name - Model Number: Azurion 3 M12 722063 722221; Azurion 3 M15 722064 722222; Azurion 5 M20 722228; Azurion 7 B12 722067 722225; Azurion 7 B20 722068 722226; Azurion 7 M12 722078 722223; Azurion 7 M20 722079 722224;
13, 133 (3,408 US; 9,725 ROW), in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
Azurion 3 M12 722063 - UDI-DI 00884838085275 or 00884838086777 Serial Numbers 108 122 131 132 56 64 84 96 98 , 722221 - UDI-DI 00884838099203 Serial Numbers 19 3 6 7 9 ; Azurion 3 M15 722064 - UDI-DI 00884838085282 Serial Numbers 201 209…
Every code shown here, 1,997 characters
Azurion 3 M12 722063 - UDI-DI 00884838085275 or 00884838086777 Serial Numbers 108 122 131 132 56 64 84 96 98 , 722221 - UDI-DI 00884838099203 Serial Numbers 19 3 6 7 9 ; Azurion 3 M15 722064 - UDI-DI 00884838085282 Serial Numbers 201 209 218 229 238 258 259 260 261 267 270 291 314 335 64 , 722222 - UDI-DI 00884838099210 Serial Numbers 12 15 17 19 23 ; Azurion 5 M20 722228 - UDI-DI 00884838099234 Serial Numbers 10 17 18 23 24 25 26 29 38 49 62 ; Azurion 7 B12 722067 - UDI-DI 00884838059290, 00884838064775, or 00884838085350 Serial Numbers 103 104 109 114 115 123 131 132 133 141 147 148 150 163 172 173 190 192 208 214 221 225 234 244 250 26 277 278 36 41 42 46 57 69 70 71 75 81 92 98 , 722225 - UDI-DI 00884838099265 Serial Numbers 28 29 37 41 53 72 ; Azurion 7 B20 722068 - UDI-DI 00884838059207, 00884838064775, 00884838085367, or 00884838101883 Serial Numbers 101 103 104 107 109 110 111 113 114 117 130 136 137 143 146 147 149 150 153 170 172 178 184 196 205 213 225 232 239 243 247 251 261 262 270 271 277 279 282 285 288 295 304 308 319 320 322 323 324 329 330 335 337 350 354 356 361 370 373 374 400 406 407 413 418 42 431 440 442 443 446 457 462 467 469 470 472 477 479 487 490 494 505 510 511 520 524 528 547 564 64 73 75 76 78 82 84 85 89 95 , 722226 - UDI-DI 00884838099272 or 00884838101883 Serial Numbers 100 105 107 108 11 112 113 117 120 121 122 123 124 125 126 127 129 139 143 144 147 153 159 173 174 180 181 19 220 255 59 67 75 78 98 ; Azurion 7 M12 722078 - UDI-DI 00884838085251 or 00884838101890 Serial Numbers 1007 121 125 136 141 143 163 165 166 170 187 215 22 224 232 239 240 249 251 256 257 258 269 271 278 279 289 290 291 292 293 294 296 298 302 305 308 309 31 317 327 359 360 364 376 379 383 384 396 399 402 410 412 415 425 436 437 438 441 445 456 465 478 479 480 481 483 488 491 493 497 500 513 520 521 522 523 524 532 535 536 537 538 539 544 545 546 550 556 557 558 559 566 571 576 585 598 603 611 612 613 626 627 635 644 645 649 654 656 657 658 661 677 679 684…
FDA’s list runs to 5,716 characters. The first part is shown; the rest is on FDA’s record.
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
Worldwide Distribution: US nationwide including states of: AL, AK, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI, WV, & WY; and OUS (International) to countries of: Afghanistan, Albania, Algeria, Argentina, Australia, Austria, Azerbaijan, Bahrain, Bangladesh, Belarus, Belgium, Bolivia, Bosnia and Herzegovina, Brazil, Brunei Darussalam, Bulgaria, Cambodia, Canada, Cayman Islands, Chile, China, Colombia, Costa Rica, Croatia, Cuba, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, Estonia, Fiji, Finland, France, French Polynesia, Gabon, Georgia, Germany, Ghana, Greece, Guadeloupe, Guinea, Honduras, Hong Kong, Hungary, Iceland, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kenya, Korea, Republic of, Kosovo, Kuwait, Kyrgyzstan, Lao People’s Democratic Republic, Latvia, Lebanon, Libya, Lithuania, Macedonia, Malaysia, Malta, Martinique, Mauritius, Mexico, Moldova, Mongolia, Morocco, Myanmar, Nepal, Netherlands, New Caledonia, New Zealand, Nicaragua, Nigeria, Norway, Oman, Pakistan, Palestine, State of, Panama, Papua New Guinea, Paraguay, Peru, Philippines, Poland, Portugal, Qatar, Reunion, Romania, Russian Federation, Saudia Arabia, Senegal, Serbia, Singapore, Slovakia, Slovenia, South Africa, Spain, Sri Lanka, Sudan, Sweden, Switzerland, Syrian Arab Republic, Taiwan, Tanzania, Thailand, Trinidad and Tobago, Tunisia, Turkey, Turkmenistan, Ukraine, United Arab Emirates, United Kingdom, Uruguay, Uzbekistan, Viet Nam, and Yemen.
The states and territories these words name
49 states and territories.
Every one of them
- Alaska
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- District of Columbia
- Delaware
- Florida
- Georgia
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- North Dakota
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- Tennessee
- Texas
- Utah
- Virginia
- Vermont
- Washington
- Wisconsin
- West Virginia
- Wyoming
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
The words say it went outside the United States too.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Ongoing, in FDA’s file.
“A recall which is currently in progress.”
openFDA, on “On-Going”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Jan 2, 2024.
- FDA classified it on Feb 16, 2024.
- FDA’s Enforcement Report published it on Feb 28, 2024.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., of Best, Netherlands.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- FDA’s list of codes runs to 5,716 characters; the first part is shown here, and the rest is on FDA’s record.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
-
U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.