Philips Medical Systems Nederland B.v.
209 recalls on record · Latest: Aug 19, 2026
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Agency notice ledger
Federal filing book Philips Medical Systems Ned… HEAVY-BOOK · SINGLE-AGENCY
#66 of 14,151 · 209 notices · 0.200% archive
- BOOK 209 notices
- RANK #66 of 14,151
- SHARE 0.200% archive
- AGENCY FDA Devices (209)
- CAT medical devices
- CATS 1 category
- LATEST Aug 19, 2026
- PHOTO Exactech, Inc.
Nearest notice-volume peer: Exactech, Inc. (2 notice gap)
Philips Medical Systems Nederland B.v. accounts for about 0.200% of the 104,423-notice archive on 209 distinct filings — a heavy share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →
How Philips Medical Systems Ned… compares to 14,151 recalling firms
Philips Medical Systems Nederland B.v. ranks 66th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.
Philips Medical Systems Ned… vs all firms by recall-notice count
Where this firm's archive sits among every tracked recalling manufacturer
209 66th of 14151 higher than 14,085 of 14,151 firms
Firms, banded by distinct federal recall-event inventory
Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13
Philips Medical Systems Ned… in the notice-volume neighbourhood
Distinct federal recall events among this firm and nearest nationwide peers
- Exactech, Inc.
Exactech, Inc.
211 notices
- Medtronic Vas…
Medtronic Vascular
211 notices
- Philips Medic… (this)
Philips Medical Systems Nederland B.v.
209 notices
- Volkswagen
Volkswagen
207 notices
- Teleflex Medi…
Teleflex Medical
204 notices
- Terumo Cardio…
Terumo Cardiovascular Systems Corporation
204 notices
What this shows Philips Medical Systems Nederland B.v. holds about 0.200% of archive notices alongside 209 distinct filings.
FDA Devices Moderate Feb 12, 2025
Azurion 7 B12 System Code: (1) 722067 (2) 722225 (3) 722235
FDA Devices Moderate Feb 12, 2025
Allura CV20 System Code: 722031
FDA Devices Moderate Feb 12, 2025
Azurion 7 B20 System Code: (1) 722068 (2) 722226 (3) 722236
FDA Devices Moderate Feb 12, 2025
AlluraXper FD20 System Code: (1) 722006 (2) 722012 (3) 722028
FDA Devices Moderate Feb 12, 2025
AlluraXperFD20/10 System Code: (1) 722029
FDA Devices Moderate Feb 12, 2025
AlluraXper FD20 Biplane System Code: (1) 722008 (2) 722013
FDA Devices Moderate Feb 12, 2025
Azurion 7 M20 System code: (1) 722224 (2) 722079 (3) 722234 (4) 722282 System Code: (1) 722078 (2) 722223 (3) 722233
FDA Devices Moderate Feb 12, 2025
AlluraXper FD20 OR Table System Code: (1) 722023 (2) 722035
FDA Devices Moderate Feb 12, 2025
AlluraXperFD20/15 System Code: (1) 722058
FDA Devices Moderate Feb 12, 2025
Azurion 5 M12 System Code: (1) 722227 (2) 722231
FDA Devices Moderate Feb 12, 2025
AlluraXper FD10/10 System Code: (1) 722005 (2) 722011 (3) 722027
FDA Devices Moderate Feb 12, 2025
Allura Xper FD10 Catalog (1) 722003 (2) 722010 (3)722026
FDA Devices Moderate Feb 12, 2025
Azurion 5 M20 System Code: (1) 722228 (2) 722232 (3) 722281
FDA Devices Moderate Feb 12, 2025
Allura Xper FD20/20 System Code: (1) 722038
FDA Devices Moderate Feb 12, 2025
Azurion 7 M12 System Code: (1) 722078 (2) 722223 (3) 722233
FDA Devices Moderate Feb 12, 2025
Azurion 3 M15 System Code: (1) 722064 (2) 722222 (3) 722280
FDA Devices Moderate Feb 12, 2025
AlluraXper FD20 Biplane OR Table System Code: (1) 722020 (2) 722025
FDA Devices Moderate Feb 12, 2025
Allura Xper FD10C System Code: (1) 722001
FDA Devices Moderate Dec 18, 2024
Philips Allura Xper Systems (R7.6-R8.1). Labeled as the following: 1. Allura Xper FD10, Model Number: 722010. 2. Allura Xper FD10/10, Model Number: 722011. 3. Allura Xper FD20, Model Number: 722012. 4. Allura Xper FD20 Biplane, Model Number: 722013. 5. Allura Xper FD10 OR Table, Model Number: 722022. 6. Allura Xper FD20 OR Table, Model Number: 722023. 7. Allura Xper FD20 Biplane OR Table, Model Number: 722025.
FDA Devices Moderate Nov 20, 2024
Philips Zenition 50, Model Number: 718096
FDA Devices Moderate Nov 20, 2024
Philips Zenition 70, Model Number: 718133
FDA Devices Moderate Sep 25, 2024
System Code Name: 722282 Azurion 7 M20 722281 Azurion 5 M20 722236 Azurion 7 B20 722235 Azurion 7 B12 722234 Azurion 7 M20 722233 Azurion 7 M12 722228 Azurion 5 M20 722227 Azurion 5 M12 722226 Azurion 7 B20 722225 Azurion 7 B12 722224 Azurion 7 M20 722223 Azurion 7 M12 722222 Azurion 3 M15 722221 Azurion 3 M12 722079 Azurion 7 M20 722078 Azurion 7 M12 722068 Azurion 7 B20 722067 Azurion 7 B12 722064 Azurion 3 M15 722063 Azurion 3 M12
FDA Devices Moderate Sep 25, 2024
System Name: 722044 INTEGRIS Allura 15-12 (biplane) 722030 Integris CV Cesar-Powerpack-Visub-Nicol 722021 INTEGRIS Allura 9 (biplane) 722018 Integris Allura 9 722017 Integris H5000 F / Allura 9F 722016 Integris H5000 C / Allura 9C
FDA Devices Moderate Sep 25, 2024
System Name: 722059 Allura Xper FD20/15 OR Table 722058 Allura Xper FD20/15 722039 Allura Xper FD20/20 OR Table 722038 Allura Xper FD20/20 722035 Allura Xper FD20 OR Table 722029 Allura Xper FD20/10 722028 Allura Xper FD20 722027 Allura Xper FD10/10 722026 Allura Xper FD10 722025 Allura Xper FD20 Biplane OR Table 722023 Allura Xper FD20 OR Table 722020 Allura Xper FD20 Biplane OR Table 722015 Allura Xper FD20 OR Table 722013 Allura Xper FD20 Biplane 722012 Allura Xper FD20 722011 Allura Xper FD1
FDA Devices Moderate Sep 25, 2024
System Name: 708038 MultiDiagnost Eleva with Flat Detector 708037 MultiDiagnost Eleva with Flat Detector 708036 MultiDiagnost Eleva 708034 MultiDiagnost Eleva with Flat Detector 708032 MultiDiagnost Eleva
FDA Devices Moderate Sep 11, 2024
Philips Azurion 7M20 systems with FlexArm ceiling-mounted system, Interventional Fluoroscopic X-Ray System, Model Numbers 722079 and 722224
FDA Devices Moderate Aug 28, 2024
Philips Allura Xper systems (R8.1 with Poly-G Stand) Interventional Fluoroscopic X-Ray System, Model Numbers 722010, 722012, 722013
FDA Devices Moderate Aug 14, 2024
Philips Azurion Interventional Fluoroscopic X-ray System with Software Version Number: R1.0, R1.1, R1.2- Intended for Image guidance in diagnostic, interventional, and minimally invasive surgery procedures for the following clinical application areas: vascular, non-vascular, cardiovascular, and neuro procedure. Model Numbers: 722063, 722064, 722067, 722068, 722078 and 722079
FDA Devices Moderate Jun 5, 2024
Philips Allura Xper FD10 system with an ADN7NT patient table. Model Number: 722010, Software Version Number 8.1.100.
FDA Devices Moderate Jun 5, 2024
Philips Allura Xper FD20 Biplane system with an ADN7NT patient table. Model Number: 722013, Software Version Number 8.1.100.
FDA Devices Moderate Jun 5, 2024
Philips Interventional Hemodynamic Application R.1.2X, R.1.3.0, R1.2.1. Software that enables invasive investigation of cardiac and vascular diseases.
FDA Devices Moderate Jun 5, 2024
Philips Allura Xper FD20 system with an ADN7NT patient table. Model Number: 722012, Software Version Number 8.1.100.
FDA Devices Moderate Feb 28, 2024
Philips Azurion Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of the affected system. Affected PCs: FlexViewing PC Azurion Model Name - Model Number: Azurion 7 B12 722067; Azurion 7 B20 722068; Azurion 7 M12 722078 722223; Azurion 7 M20 722079;
FDA Devices Moderate Feb 28, 2024
Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of affected systems. Affected PCs: FlexVision PC Allura Xper Model Name - Model Number: Allura Xper FD10 722003 722010 722026; Allura Xper FD10/10 722005 722011 722027; Allura Xper FD20 722006 722012 722028; Allura Xper FD20 Biplane 722008 722013; Allura Xper FD20 Biplane OR Table 722025; Allura Xper FD20 OR Table 722023 722035; Allura Xper FD20/10
FDA Devices Moderate Feb 28, 2024
Azurion 7 with a Certeray generator-To perform image guidance in diagnostic, interventional, and minimally invasive surgery procedures Models: (1) 722223, (2) 722224, (3) 722225, (4) 722226
FDA Devices Moderate Feb 28, 2024
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;
FDA Devices Moderate Feb 28, 2024
Azurion 3 with a Certeray generator -To perform image guidance in diagnostic, interventional, and minimally invasive surgery procedures Models: (1) 722221 (2) 722222 (3) 722280
FDA Devices Moderate Feb 28, 2024
Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of affected systems. Affected PCs: Imaging Processing PC, Host PC, FlexVision PC Allura Xper Model Name - Model Number: Allura Xper FD10 722003 722010 722026; Allura Xper FD10 OR Table 722022; Allura Xper FD10/10 722005 722011 722027; Allura Xper FD10C 722001; Allura Xper FD20 722006 722012 722028; Allura Xper FD20 Biplane 722008 722013; Allura Xper FD20 Biplan
FDA Devices Moderate Feb 28, 2024
Azurion 5 with a Certeray generator-To perform image guidance in diagnostic, interventional, and minimally invasive surgery procedures Models: (1) 722227 (2) 722228
FDA Devices Moderate Feb 28, 2024
Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the DIMMs (Dual In-line Memory Modules) used with affected systems. Allura Xper Model Name - Model Number: Allura Xper FD10 722003 722010 722026; Allura Xper FD10/10 722005 722011 722027; Allura Xper FD10C 722001; Allura Xper FD20 722006 722012 722028; Allura Xper FD20 Biplane 722008 722013; Allura Xper FD20 Biplane OR Table 722025; Allura Xper FD20 OR Table 722023 722035; Allura Xper FD20/1
FDA Devices Moderate Feb 7, 2024
Philips Azurion system, Interventional fluoroscopic x-ray system. System Product Name - Model Numbers Azurion 3M12 -722063, 722221; Azurion 3M15 - 722064, 722222; Azurion 5M12 - 722227; Azurion 5M20 - 722228; Azurion 7B12/12 - 722067, 722225; Azurion 7B20/15 - 722068, 722226; Azurion 7M12 - 722078, 722223; Azurion 7M20 - 722079, 722224; Azurion 3 M15 (China) - 722280;
FDA Devices Moderate Feb 7, 2024
Azurion 7 M20 FlexArm system (Software version R2.x) with Maquet Magnus Table (Software version 05.02.12)
FDA Devices Moderate Feb 7, 2024
Azurion 7 M20 FlexArm system (Software version R2.x) with Maquet Magnus Table (Software version 05.02.12)
FDA Devices Moderate Dec 27, 2023
Philips Azurion systems with monoplane fixed ceiling mounts: 722078 Azurion 7 M12 722079 Azurion 7 M20 722223 Azurion 7 M12 722224 Azurion 7 M20 722227 Azurion 5 M12 722228 Azurion 5 M20
FDA Devices Moderate Dec 27, 2023
Philips Allura systems with monoplane fixed ceiling mounts: 722001 Allura Xper FD10C 722003 Allura Xper FD10 722006 Allura Xper FD20 722010 Allura Xper FD10 722012 Allura Xper FD20 722015 Allura Xper FD20 OR Table 722016 Integris H5000 C / Allura 9C 722018 Integris Allura 9 722022 Allura Xper FD10 OR Table 722023 Allura Xper FD20 OR Table 722026 Allura Xper FD10 722028 Allura Xper FD20 722033 Allura Xper FD10 OR Table 722035 Allura Xper FD20 OR Table 722043 Integris Allura 15 & 1
FDA Devices Moderate Sep 20, 2023
Philips Allura Xper, Allura Centron, Allura CV, Azurion, UNIQ Clarity, and MultiDiagnost-Eleva systems
FDA Devices Moderate Sep 13, 2023
Allura Xper series
FDA Devices Moderate Sep 13, 2023
Azurion
FDA Devices Moderate Sep 13, 2023
MultiDiagnost-Eleva
FDA Devices Moderate Sep 6, 2023
Wireless Foot Switch distributed with Philips Allura Xper and Azurion Interventional Fluoroscopic X-Ray Systems
Philips Medical Systems Ned… carries an outsized archive share
Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.
Similar recall count
Nearest multi-notice firms by distinct-event totals (209 here — heavy-book).
Similar medical devices volume
Nearest multi-notice firms in the same narrow category lane.
Frequently Asked Questions
How many federal recall notices name Philips Medical Systems Ned…? ▼
PlainRecalls indexes 209 distinct federal recall events naming Philips Medical Systems Nederland B.v., aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Philips Medical Systems Ned… sit among other recalling firms? ▼
Philips Medical Systems Nederland B.v. ranks #66 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Philips Medical Systems Ned…'s notices? ▼
FDA Devices accounts for 209 of this firm's 209 indexed notices.
What product category dominates Philips Medical Systems Ned…'s filing book? ▼
Filings for Philips Medical Systems Nederland B.v. span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Philips Medical Systems Nederland B.v.: 209 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.
Firm-level totals aggregate distinct federal recall events naming Philips Medical Systems Nederland B.v.; individual notices remain authoritative on each linked recall page.
Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026