Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland Blames BIOS Battery Design Flaw in Allura Centron 722400 Recall (Z
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The BIOS
suffocation risk Recalls
495 recalls tagged with “suffocation risk”.
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
Northeast Scientific Recalled 561 Units of NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy C
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
Northeast Scientific
Potential for
Health & Personal Care
HIGH
FDA DEVICE
Northeast Scientific NES Reprocessed 0.9mm Turbo Elite Laser Atherectomy Catheter Recall 2025
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
Northeast Scientific
Potential for
Health & Personal Care
HIGH
FDA DEVICE
Northeast Scientific NES Reprocessed 1.4mm OTW Turbo Elite Laser Atherectomy Catheter Recall 173 Un
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
Northeast Scientific
Potential for
Health & Personal Care
HIGH
FDA DEVICE
NES Reprocessed 1.7mm RX Turbo Elite Laser Atherectomy Catheter Recall: 616 Units In US Distribution
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
Northeast Scientific
Potential for
Health & Personal Care
HIGH
FDA DEVICE
Northeast Scientific Laser Atherectomy Catheter Recalled for Sterile Barrier Breach Risk (2025)
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
Northeast Scientific
Potential for
Health & Personal Care
HIGH
FDA DEVICE
Northeast Scientific Recalled 1,019 Reprocessed Turbo Elite Atherectomy Catheters Over Sterility Bre
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
Northeast Scientific
Potential for
HIGH
Health & Personal Care
HIGH
FDA DRUG
Granules Pharmaceuticals Recalls 3,384 Bottles of Dextroamphetamine ER Capsules for Impurity Issues
Granules Pharmaceuticals
Failed Impurities/Degradation
HIGH
CPSC
CT-ENERGY Recalls nc-02 Lithium Coin Battery Chargers Over Battery Ingestion Risk (2025)
CT-ENERGY
The recalled
MEDIUM
CPSC
DT Swiss Recalls Carbon Wheels Over Crash Hazard Affecting 2740000 ID Codes and Higher (2025)
DT Swiss
A defect
Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific Extractor Pro RX Balloon Catheter Recalled Over Labeling Error (2025)
The product in incorrectly labeled. The label indicates that the skive hole should be above the balloon, while it is actually positioned below, and vice versa.
Boston Scientific
The product
Health & Personal Care
HIGH
FDA DEVICE
Siemens Medical Solutions USA BIOGRAPH One MRI System Recalled for Helium Leak Risk (1 Unit, 2025)
Siemens Medical Solutions USA
There is
Health & Personal Care
HIGH
FDA DEVICE
Howmedica Osteonics Recalls 55 EXETER V40 Surgical Stems Due to Product Mix Risk
a potential product mix where the package labeled as Catalog Number 0580-1-442, lot A00976, may contain Catalog Number 0580-1-352, lot G8754849, and vice versa. Patient labels may also be impacted.
Howmedica Osteonics
a potential
Health & Personal Care
HIGH
FDA DEVICE
Siemens MAGNETOM Cima.X MRI Recall: 9 Units Worldwide (2025)
Siemens Medical Solutions USA
There is
Health & Personal Care
HIGH
FDA DEVICE
Siemens MAGNETOM Verio Dot Upgrade MRI Recalled Over Ice Blockage Risk (46 Units) 2025
Siemens Medical Solutions USA
There is
Health & Personal Care
HIGH
FDA DEVICE
Siemens MAGNETOM Connectom.X MRI Recalled Globally Over Ice Blockage in Vent System
Siemens Medical Solutions USA
There is
Health & Personal Care
HIGH
FDA DEVICE
Siemens MAGNETOM Spectra MRI Recalled, Ice Blockage in Venting May Cause Helium Leak (2025)
Siemens Medical Solutions USA
There is
Health & Personal Care
HIGH
FDA DEVICE
Siemens MAGNETOM Lumina MRI System Recall Covers 71 Units Worldwide for Ice Blockage Risk
Siemens Medical Solutions USA recalled 71 MAGNETOM Lumina MRI systems worldwide, including US and 50+ countries, due to ice blockage in the magnet venting system that could cause a helium leak during a quench.
Siemens Medical Solutions USA
There is
Tag Statistics
Total Recalls
495