Health & Personal Care
HIGH
FDA DEVICE
Penner Patient Care Recalls 15 Penner Pacific Bathing Spa Devices for Missing UDI (2025)
The device does not bear a unique device identifier.
Penner Patient Care
The device
immediate action Recalls
2,756 recalls tagged with “immediate action”.
Health & Personal Care
HIGH
FDA DEVICE
Penner Pacific Bathing Spa Recalled for Missing Unique Device Identifier (UDI) in 206 Units
The device does not bear a unique device identifier.
Penner Patient Care
The device
Health & Personal Care
HIGH
FDA DEVICE
Penner Patient Care Bathing Spa Devices Recall for Missing Unique Device Identifier (Z-1500-2026)
The device does not bear a unique device identifier.
Penner Patient Care
The device
Health & Personal Care
HIGH
FDA DEVICE
Siemens Artis Pheno Fluoroscopic X-Ray System Recalled for 20 Units in 2025
Limited system movements after startup .
Siemens Medical Solutions USA
Limited system
Health & Personal Care
HIGH
FDA DEVICE
Max Mobility Permobil MX2+ SpeedControl Dial Recalled for 15,834 Units in 2025
Due to a faulty electrical connection between the speed control Dial and the wheelchair motor, their is a potential for lost of control of the device potentially resulting in minor or major injuries.
Max Mobility
Due to
Health & Personal Care
HIGH
FDA DRUG
Viona Pharmaceuticals Recalls Tavaborole Topical Solution 5% Over Discoloration (2025)
TAVABOROLE
Discoloration
Health & Personal Care
HIGH
FDA DEVICE
Max Mobility/Permobil Recalls 8,413 Smart Drive MX2+ SpeedControl Dials (2025)
Due to a faulty electrical connection between the speed control Dial and the wheelchair motor, their is a potential for lost of control of the device potentially resulting in minor or major injuries.
Max Mobility
Due to
Food & Beverages
HIGH
FDA FOOD
Domino Foods Recalls 4,500 Bags of Pure Cane Granulated Sugar Over Contamination Risk (2025)
Domino Foods recalled 4,500 bags of Pure Cane Granulated Sugar distributed in California and Utah. The sugar may contain foreign objects. Consumers should stop using it and contact Domino Foods for refund or replacement.
Domino Foods
Potential contamination
Food & Beverages
HIGH
FDA FOOD
H & N Group Frozen Shrimp Recalled for Cs-137 Contamination (2025)
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)
H & N Group
Product manufactured
Health & Personal Care
HIGH
FDA DEVICE
Max Mobility/Permobil Recalls 25,389 MX2+ SpeedControl Dial Units (2025)
Due to a faulty electrical connection between the speed control Dial and the wheelchair motor, their is a potential for lost of control of the device potentially resulting in minor or major injuries.
Max Mobility
Due to
Food & Beverages
HIGH
FDA FOOD
Baker's Authority Everything Bagel Mix Recall Affects 197 Units for Sesame Allergy Risk
Product label does not list ingredients including major food allergen: sesame. Additional undeclared ingredients include: poppy seeds, dried garlic, dried onion, and sea salt
Baker's Authority
Product label
Food & Beverages
HIGH
FDA FOOD
Baker's Authority Recalls 78 Units of Three Seed Mix for Sesame Allergen (2025)
Product label does not list ingredients including major food allergen: sesame. Additional undeclared ingredients include: millet and flax
Baker's Authority
Product label
Health & Personal Care
HIGH
FDA DEVICE
Applied Medical Technology NutraGlide ENFit Nasal Feeding Tube Recall — 200 Units (2025)
The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
Applied Medical Technology
The nasal
Health & Personal Care
HIGH
FDA DEVICE
Applied Medical Technology NutraGlide ENFit Nasal Feeding Tube Recall 840 Units (2025)
The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
Applied Medical Technology
The nasal
Health & Personal Care
HIGH
FDA DEVICE
Applied Medical Technology Recalls NutraGlide ENFit Nasal Feeding Tube 5F-6F x 55 in (1,780 units)
Applied Medical Technology recalled 1,780 NutraGlide ENFit nasal feeding tubes distributed in Massachusetts and Rhode Island. Distal tips on these devices may detach at lower than expected forces. Stop using immediately and follow the recall instructions.
Applied Medical Technology
The nasal
Health & Personal Care
HIGH
FDA DEVICE
Applied Medical Technology NutraGlide ENFit Nasal Feeding Tubes Recalled for 390 Units in 2025
The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
Applied Medical Technology
The nasal
Health & Personal Care
HIGH
FDA DEVICE
Agilent Technologies Denmark ApS Recalls 67 FLEX CD20 Antibody for Potential Weak Staining
Their is the potential for weak staining which may result in false negative CD20 identification.
Agilent Technologies Denmark ApS
Their is
Health & Personal Care
HIGH
FDA DEVICE
Agilent Technologies Recalls 65 FLEX Monoclonal CD20 Antibodies Over Weak Staining Risk (GA60461-2CN
Their is the potential for weak staining which may result in false negative CD20 identification.
Agilent Technologies Denmark
Their is
Health & Personal Care
HIGH
FDA DRUG
Lannett Lisdexamfetamine Recall Alerts 40 mg Capsules for Label Mix-Up (2025)
Labeling: Label Mix-up. A bottle labeled as Lisdexamphetamine Dimesylate Capsules 40mg, contained Lisdexamphetamine Dimesylate Capsules 30mg.
Lisdexamfetamine Dimesylate
Labeling: Label
Health & Personal Care
HIGH
FDA DEVICE
Agilent FLEX Monoclonal CD20 Antibody Recalled for 4,145 Units (2025)
Their is the potential for weak staining which may result in false negative CD20 identification.
Agilent Technologies
Their is
Tag Statistics
Total Recalls
2,756