Health & Personal Care
HIGH
FDA DEVICE
Penner Patient Care Penner Pacific Bathing Spa Recalled for Missing UDI (158 Units)
The device does not bear a unique device identifier.
Penner Patient Care
The device
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
Change Healthcare Radiology Solutions Software Version 14.2.2 Recalled for Incomplete Reports
Due to software issue, radiology reports may not be fully displayed when viewing.
CHANGE HEALTHCARE CANADA
Due to
Health & Personal Care
HIGH
FDA DEVICE
Penner Patient Care Bathing Spa Recalled for Missing UDI in 2025
The device does not bear a unique device identifier.
Penner Patient Care
The device
Health & Personal Care
HIGH
FDA DEVICE
Penner Pacific Bathing Spa Recall: 10 Units Missing UDI (2025)
The device does not bear a unique device identifier.
Penner Patient Care
The device
Health & Personal Care
HIGH
FDA DEVICE
Penner Patient Care Penner Pacific Bathing Spa Recalled for Missing UDI (25 Units, 2025)
The device does not bear a unique device identifier.
Penner Patient Care
The device
Health & Personal Care
HIGH
FDA DEVICE
Penner Patient Care Recalls 26 Penner Pacific Bathing Spa Units for Missing UDI Label (2026)
The device does not bear a unique device identifier.
Penner Patient Care
The device
Health & Personal Care
HIGH
FDA DEVICE
Penner Patient Care's Penner Pacific Bathing Spa Recalled for Missing UDI in 21 Units (2025)
The device does not bear a unique device identifier.
Penner Patient Care
The device
Health & Personal Care
HIGH
FDA DEVICE
Penner Pacific Bathing Spa Recalled for Missing Unique Device Identifier in 190 US Units (2025-2026)
Penner Patient Care recalls 190 Bathing Spa devices nationwide after discovering the units lack a unique device identifier. The issue involves missing UDI on the device. Stop using the device immediately and follow the recall instructions.
Penner Patient Care
The device
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
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
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
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
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 DRUG
Viona Pharmaceuticals Recalls Tavaborole Topical Solution 5% Over Discoloration (2025)
TAVABOROLE
Discoloration
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 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
Baker’s Authority Graham Cracker Meal Recalled for Undeclared Allergens in 5lb Bags (2025)
Baker’s Authority recalled 70 units of Graham Cracker Meal on August 12, 2025. The product ships to multiple states. Undeclared wheat and soy allergens are listed on the label. The recall urges consumers to avoid consumption and seek refunds or replacements.
Bakers Authority
Product label
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