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
stop use immediately Recalls
2,229 recalls tagged with “stop use immediately”.
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 FD20 Biplane OR Table Recall for BIOS Battery Depletion (2025)
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The BIOS
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
Inpeco Recall: 8 FlexLab FLX Potassium Test System Units Over Unverified HIL Function (2025)
Inpeco
The FlexLab
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 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
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 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 DRUG
Fagron Compounding Services Bevacizumab Syringe Recall Affects 109,320 Units Nationwide
Lack of Assurance of Sterility
Fagron Compounding Services
Lack of
Food & Beverages
HIGH
FDA FOOD
Tas Tematic Foods Frozen Shrimp IQF 2-lb Bags Recalled for Nitrofuran Contamination (2025)
Product which was on FDA hold for high levels of Nitrofuran was inadvertently distributed.
Tas Tematic Foods
Product which
Health & Personal Care
HIGH
FDA DEVICE
Baxter Healthcare Recalls 49,200 CONTINU-FLO IV Solution Sets for Leakage Risk (2025)
Baxter Healthcare recalls 49,200 CONTINU-FLO IV Solution Sets distributed nationwide in the United States. IV sets may leak. Healthcare facilities and patients should stop using the device immediately and follow Baxter's recall instructions.
Baxter Healthcare
IV sets
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 NES Turbo Elite Laser Atherectomy Catheter Recall: 199 Units (2025)
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
Northeast Scientific
Potential for
Health & Personal Care
HIGH
FDA DEVICE
Baxter CLEARLINK Paclitaxel IV Set Recalled for Leak Hazard in 2025 (27,072 Units)
Baxter
IV sets
Health & Personal Care
HIGH
FDA DEVICE
Baxter Healthcare Recalls 8,368 CLEARLINK CONTINU-FLO IV Sets for Leakage Risk (2025)
Baxter Healthcare
IV sets
Health & Personal Care
HIGH
FDA DEVICE
Baxter Healthcare CLEARLINK CONTIN-FLO IV Infusion Sets Recalled for Leaks (106,176 Units)
Baxter Healthcare
IV sets