Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20 BiOS Battery Recall Affects 5,067 Units Worldwide
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The BIOS
Category hub
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
Beckman Coulter Phosphorus Reagent Recall: 2,146 Units for Calibration Failures
Specific SYNCHRON Systems Modular Chemistry Phosphorus (PHOSm REF 467868) reagent lots may fail calibration before the lot expiration date which causes a delay in obtaining patient results.
Beckman Coulter
Specific SYNCHRON
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 Biplane Recalled for BIOS Battery Failure in 501 Units (2025)
Philips Medical Systems Nederland
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland Faces High-Risk Recall for Allura Xper FD20/15 BIOS Battery
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland recalls 5 Allura Xper FD20/20 OR Tables for BIOS battery startup
Philips Medical Systems Nederland B.V.
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems FD20 Biplane OR Table Recall for BIOS Battery Depletion (2025)
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD10C Recall for 2 US Units Over BIOS Battery Startup Failure (2025)
Philips Medical Systems Nederland B.V.
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD10 Recalled for BIOS Battery Startup Failure (2,317 Units Worldwide, 2025)
Philips Medical Systems Nederland
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
PHILIPS Allura Xper FD10/10 Recall Tied to BIOS Battery Depletion
Philips Medical Systems Nederland B.V.
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Philips Recalling 298 Allura Xper FD20 OR Tables Worldwide Over BIOS Battery Risk (2025)
Philips
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland Recall: BIOS Battery Causes Startup Failures in Allura Xper CV20 7
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Inpeco Recall: 8 FlexLab FLX Potassium Test System Units Over Unverified HIL Function (2025)
Inpeco
The FlexLab
Health & Personal Care
HIGH
FDA DRUG
High-Risk Antibiotic Recall: Sulfamethoxazole and Trimethoprim 800/160 mg Double Strength Packets Re
Presence of a Foreign Substance: A specific lot of auxiliary polyester coil, used in product packaging by manufacturer (Amneal Pharmaceuticals LLC) was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
SULFAMETHOXAZOLE AND TRIMETHOPRIM
Presence of
Health & Personal Care
HIGH
FDA DRUG
Major Pharmaceuticals Sulfamethoxazole and Trimethoprim 800 mg/160 mg 100-Tablets Recall 2025
Presence of a Foreign Substance: A specific lot of auxiliary polyester coil, used in product packaging by manufacturer (Amneal Pharmaceuticals LLC) was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Sulfamethoxazole and Trimethoprim
Presence of
Health & Personal Care
HIGH
FDA DEVICE
LeMaitre Vascular Artegraft Collagen Vascular Grafts Recall 2025: 28 U.S. Units Affected
The bovine carotid arteries used to produce the impacted grafts from affected lots were sourced using raw material from a supplier that had not been reviewed and approved by the appropriate regulatory authority.
LeMaitre Vascular
The bovine
Health & Personal Care
HIGH
FDA DRUG
AvKARE Norgestimate and Ethinyl Estradiol Tablets Recall for Uniformity Issue (2025)
AvKARE
Failed Content
Health & Personal Care
HIGH
FDA DEVICE
Canon Medical System SPOT Fluoro Digital Radiography System Recall Affects 8 Units in US (2025)
Canon Medical System
It has
Health & Personal Care
HIGH
FDA DRUG
Fagron Compounding Services Bevacizumab Syringe Recall Affects 109,320 Units Nationwide
Lack of Assurance of Sterility
Fagron Compounding Services
Lack of
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
Related Categories
Category Statistics
Total Recalls
1,882
Pages
95