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
These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
Immediate attention
High Risk Recalls
4,262 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
- High-risk recalls
- 4,262
- Action level
- Stop use
What to do if you own a recalled product
- Stop using the product immediately
- Keep the product away from children
- Follow the remedy instructions provided
- Contact the manufacturer for a refund or replacement
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
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
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 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 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
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 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
BigTree Sales Recalls BT-GERMWAND-LRG-WHT UV-C Wand for Unsafe Radiation Risk (2025)
BigTree Sales
The subject
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
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
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
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
Baxter Healthcare Recalled 473,040 CLEARLINK IV Solution Sets for Leakage Risk (2025)
Baxter Healthcare
IV sets
Health & Personal Care
HIGH
FDA DEVICE
ConvaTec DuoDERM Extra Thin Dressings Recalled in 2025 for Foreign Matter
Wound dressing may have foreign matter on the product.
ConvaTec
Wound dressing
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 18,720 CLEARLINK Non-DEHP IV Sets for Leakage Risk (2025)
Baxter Healthcare
IV sets