SCNHD LA L7-4 HDI Transducer Probe
Pending LLM rewrite. Source: FDA_DEVICE Z-2400-2025.
- Product
- SCNHD LA L7-4 HDI Transducer Probe
- Category
- Medical Device
- Distribution
- Distributed nationwide
Manufacturer
101 recalls in our database name Philips Ultrasound, Inc as the manufacturing or recalling firm.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
Pending LLM rewrite. Source: FDA_DEVICE Z-2400-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2385-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2368-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2366-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2370-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2049-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2054-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2064-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2062-2025.
Philips Ultrasound is recalling Philips S5-1 Transducers because they were refurbished beyond their useful life, which may affect device performance and safety.
Pending LLM rewrite. Source: FDA_DEVICE Z-2063-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2066-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2060-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2065-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2057-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2067-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2061-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2048-2025.
Philips Ultrasound, Inc. is recalling Philips C9-5EC transducer devices that were refurbished beyond their useful life, which may affect device performance and safety.
Philips Ultrasound is recalling approximately 5,230 eL18-4 EMT ultrasound transducers that were refurbished beyond their useful life, which may affect device performance or safety.
Philips Ultrasound, Inc. is recalling Philips C5-2 Transducers because they were refurbished beyond their useful life. The affected devices were distributed domestically nationwide and internationally across 49 countries.
Philips Ultrasound, Inc. is recalling Philips XL14-3 Transducers because they were refurbished beyond their useful life, which may affect device performance and patient safety during ultrasound examinations.
Philips Ultrasound, Inc. is recalling Philips S7-2 Transducer ultrasound devices that were refurbished beyond their useful life. The affected devices have been distributed domestically and internationally.
Philips Ultrasound is recalling 5,230 L8-4 transducer units that were refurbished beyond their useful life, which may affect device safety and performance. The units were distributed nationwide and internationally.
Philips Ultrasound is recalling Philips eL18-4 Transducers because they were refurbished beyond their useful life, which may affect device performance and patient safety.