Health & Personal Care
HIGH
FDA DEVICE
Iantrek CycloPen CP-300 Cyclodialysis System Recalled for Sterile Packaging Integrity (2025)
Potential for compromised integrity of the sterile packaging.
Iantrek
Potential for
electronic Recalls
325 recalls tagged with “electronic”.
Health & Personal Care
HIGH
FDA DEVICE
Philips Ultrasound X3-1 Transducer Recalled for Labeling Clarification in 2026 (17 Units)
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips Ultrasound
To provide
Health & Personal Care
HIGH
FDA DEVICE
GE Medical Systems AW Server 2.0, AW Server 3.0, 3.1, 3.2 Recalled For Security Breach Risk (2025)
Firm has identified a security vulnerability in AW Server products. If exploited, a malicious actor could compromise the confidentiality, integrity, and availability of patient data.
GE Medical Systems
Firm has
Health & Personal Care
HIGH
FDA DEVICE
Philips Ultrasound S5-2 Transducer Recall 2025 - 1 Unit Nationwide
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips Ultrasound
To provide
Health & Personal Care
HIGH
FDA DEVICE
Philips Ultrasound C9-4 Transducer Recalled for Lifespan Labelling — 1 Unit (2025)
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips Ultrasound
To provide
Health & Personal Care
HIGH
FDA DEVICE
GE Healthcare CSCS V3 MAS800 Central Station Recalled for 2,306 Units Worldwide (2025)
GE Healthcare
GE HealthCare
Health & Personal Care
HIGH
FDA DEVICE
Spacelabs Healthcare Recalling 8,179 DVI Display Cables Over EMI Interference Risk (2025)
Spacelabs Healthcare
Due to
Health & Personal Care
HIGH
FDA DEVICE
Philips X7-2 Ultrasound Transducer Recall for 5 Units Nationwide (2026)
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips Ultrasound
To provide
Health & Personal Care
HIGH
FDA DEVICE
Philips Ultrasound OMNI II TEE Transducer Recall Two Units Nationwide (2025)
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips Ultrasound
To provide
Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems Recalls 32,433 Basic Biopsy Trays Re-Gassed After EO Sterilization (2025)
American Contract Systems
Identified products
Food & Beverages
HIGH
FDA FOOD
Pacific Coast Producers Fruit Cocktail Recalled for Lead Contamination in 15 oz Cans (609 cases)
Potential contamination with heavy metal (Lead).
Pacific Coast Producers
Potential contamination
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20 OR Table Recalled for 174 Units Worldwide in 2025
Philips Medical Systems Nederland
Systems may
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20/10 Recall 45 Units Worldwide in 2025
Philips Medical Systems Nederland B.V.
Systems may
Health & Personal Care
HIGH
FDA DEVICE
Inpeco FlexLab X System Potassium Test System Recalled for Unvalidated Hemolysis, Icterus, Lipemia H
Inpeco S.A.
The FlexLab
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20/20 Recall 115 Units Over Startup-Battery Risk (2025)
Philips Medical Systems Nederland
The BIOS
Food & Beverages
HIGH
FDA FOOD
New Spirit Naturals Recalled 178 Units of Super Muscle Support Powder for Milk Allergen (2025)
New Spirit Naturals
undeclared allergen
Food & Beverages
HIGH
FDA FOOD
New Spirit Naturals Protein Powder Recall Affects 79 Units Over Milk Allergen Disclosure
New Spirit Naturals
undeclared allergen
Health & Personal Care
HIGH
FDA DEVICE
BigTree Sales Recalls BT-GERMWAND-LRG-WHT UV-C Wand for Unsafe Radiation Risk (2025)
BigTree Sales
The subject
Health & Personal Care
HIGH
FDA DEVICE
Getinge 88-Series Washer-Disinfector 88-5 Recalled for Overheat Risk in 788 Units (2025)
Potential for device to overheat during operation f the circulation pressure calibration was not performed or had been performed incorrectly, and the low-pressure alarm is not triggered.
Getinge Disinfection Ab
Potential for
Health & Personal Care
HIGH
FDA DEVICE
Baxter Healthcare Recalled 69,936 CLEARLINK IV Extension Sets for Leak Risk (2025)
Baxter Healthcare recalled 69,936 CLEARLINK System Non_DEHP Extension Sets sold nationwide to hospitals and clinics. The IV extension sets may leak. Healthcare providers should stop using the device and follow Baxter's recall instructions.
Baxter Healthcare
IV sets