Health & Personal Care
HIGH
FDA DRUG
Viorele Desogestrel/Ethinyl Estradiol Recall 2025 for Impurities
Viorele
Failed Impurities/Degradation
immediate action Recalls
2,756 recalls tagged with “immediate action”.
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 BiOS Battery Recall Affects 5,067 Units Worldwide
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland Recall Expands for Allura Xper FD20/15 OR Table Model 722059 (2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The BIOS
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
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
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 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 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
Food & Beverages
HIGH
FDA FOOD
ICF Factory Recalls 12 Pints Vanilla G. Nutt Ice Cream Over undeclared Almond (2025)
ICF Factory
May contained
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
Health & Personal Care
HIGH
FDA DEVICE
Baxter Healthcare Recalled 473,040 CLEARLINK IV Solution Sets for Leakage Risk (2025)
Baxter Healthcare
IV sets
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 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
Health & Personal Care
HIGH
FDA DEVICE
ImaCor ClariTEE Miniaturized TEE Probe CLT-010 Recalled Over Reversed Articulation Risk (2025)
Production assembly error resulting in the potential for reversed articulation, where moving the lever forward caused the probe tip to anteflex rather than retroflex, and vice versa.
ImaCor
Production assembly
Food & Beverages
HIGH
FDA FOOD
Herbal Creations Colostrum Powder Recall for Milk Allergen Labeling Error (2025)
Bulk packaged dietary ingredient manufacturer product label does not declare Milk as an allergen ingredient.
Herbal Creations
Bulk packaged
Health & Personal Care
HIGH
FDA DEVICE
Baxter Healthcare Recalls 8,368 CLEARLINK CONTINU-FLO IV Sets for Leakage Risk (2025)
Baxter Healthcare
IV sets
Tag Statistics
Total Recalls
2,756