PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Recall: Azurion 3 M12 System Code: (1) 722063 (2) 7
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Recall: Azurion 3 M12 System Code: (1) 722063 (2) 7 is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.; Product: Azurion 3 M12 System Code: (1) 722063 (2) 722221; Reason for recall: Potential safety issue with t
| Recalling firm | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
|---|---|
| Product | Azurion 3 M12 System Code: (1) 722063 (2) 722221 |
| Reason for recall | Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Ongoing |
| Distribution | Worldwide distribution - US Nationwide and the countries of Canada, Afghanistan, Albania, Algeria, Argentina, Armenia, Australia, Austria, Azerbaijan, Bahrain, Bangladesh, Belarus, Belgium, Bolivia, Bosnia and Herzegovina, Brazil, Brunei Darussalam, Bulgaria, Cambodia, Cayman Islands, Chile, China, |
| Recall initiated | 20250113 |
| Recall number | Z-1087-2025 |
| Category | device |
| Country | Netherlands |
$29/mo
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