Health & Personal Care
HIGH
FDA DEVICE
Spacelabs Healthcare DVI Display Cables Recalled for EMI Risk in 16,898 Units (2025)
Spacelabs Healthcare
Due to
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Health & Personal Care Recalls
1,882 product recalls found in this category. Browse active safety alerts and related categories from the same official source network.
- Active recalls
- 1,882
- Pages
- 95
High activity category
This category has a significant number of recalls. Check it regularly if you own products in this area.
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
LOW
FDA DEVICE
Philips S4-1 Ultrasound Transducer Recall: 41 Units Nationwide in 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 DRUG
Endo USA Recalls 1,041 Cartons of Everolimus 5mg Tablets Over IP-C Impurity (2025)
Failed Impurities/Degradation Specifications: Out of specification for impurity IP-C.
Everolimus
Failed Impurities/Degradation
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
Philips Ultrasound OMNI III TEE Transducer Recall for Labelling Clarification (75 Units) 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
Philips Recal Size 40 L12-5 Ultrasound Transducers for Labeling Life Span Recall (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 L17-5 Transducer Recalled for Useful-Life Labeling (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
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
LOW
FDA DEVICE
Philips 3D6-2 Ultrasound Transducer Recalled for Labeling Clarification (17 Units, 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
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 Recalled 11 Mini Multi TEE Transducers Over Useful-Life Labeling (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
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 DRUG
Zydus Lifesciences Entecavir 0.5 mg Tablets Recalled Nationwide for Impurity Degradation Failures (D
Zydus Lifesciences Ltd.
Failed Impurity/Degradation
Health & Personal Care
HIGH
FDA DRUG
Zydus Lifesciences Entecavir 1 mg Tablets Recalled for Impurity Degradation Issues (2025)
Zydus Pharmaceuticals USA Inc.
Failed Impurity/Degradation
Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems High-Index Medical Kits Recalled for Re-Gassing After EO Sterilization Non
American Contract Systems
Identified products
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
Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems Basic Biopsy Tray Recalled for Re-Gassing Hazard (32,433 Units) 2025Recall
American Contract Systems
Identified products
Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems Recalling 32,433 UDPG88W PICC G-TUBE Pack in 2025 Recall
American Contract Systems
Identified products
Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems Recalls 32,433 Cardiac Cath Lab Kits Due to Re-Gassed Sterilization Risk (
American Contract Systems
Identified products
Related Categories
Category Statistics
Total Recalls
1,882
Pages
95