HIGH
FDA DEVICE
Penner Pacific Bathing Spa, Model Numbers 760010-1, 770010-1
The device does not bear a unique device identifier.
Penner Patient Care
The device
All Product Recalls
Browse through 2,852 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
HIGH
FDA DEVICE
Penner Pacific Bathing Spa, Model Numbers 360020-1P
The device does not bear a unique device identifier.
Penner Patient Care
The device
Food & Beverages
HIGH
FDA FOOD
Wegmans Cheese Flight Recalled Due to Listeria Contamination
Wegmans Food Markets recalled 4,884 units of its Assorted Cheese Flight on August 12, 2025. The product may be contaminated with Listeria monocytogenes, a serious foodborne pathogen. The recall affects consumers in NY, PA, MA, NJ, MD, VA, NC, DE, CT, and DC.
Wegmans Food Markets
Products may
Health & Personal Care
HIGH
FDA DEVICE
Max Mobility Recalls Smart Drive MX2+ Due to Control Hazard
Max Mobility recalled 8,413 Smart Drive MX2+ SpeedControl Dials on August 12, 2025. A faulty electrical connection poses a risk of losing control of the wheelchair, leading to potential injuries. Healthcare providers should stop using the device immediately and follow recall instructions.
Max Mobility
Due to
Health & Personal Care
HIGH
FDA DEVICE
Max Mobility Recalls Smart Drive MX2+ Due to Control Hazard
Max Mobility recalled 15,834 Smart Drive MX2+ SpeedControl Dials on August 12, 2025. A faulty electrical connection may lead to loss of control, causing injuries. Users should stop using the device immediately and follow recall instructions.
Max Mobility
Due to
Food & Beverages
HIGH
FDA FOOD
Baker's Authority Everything Bagel Mix Recalled Over Allergen Risk
Baker's Authority recalled 197 units of Everything Bagel Mix on August 12, 2025. The product fails to list sesame, a major food allergen, on its label. Consumers should avoid consumption and seek refunds.
Bakers Authority
Product label
Food & Beverages
HIGH
FDA FOOD
Wegmans Camembert Cheese Recalled Due to Listeria Risk
Wegmans Food Markets recalled 4,884 units of Medium Camembert Soft Ripened Cheese on August 12, 2025. The product may be contaminated with Listeria monocytogenes, posing a serious health risk. Consumers should not eat the cheese and should contact the company for refunds.
Wegmans Food Markets
Products may
Food & Beverages
HIGH
FDA FOOD
Wegmans Brie Cheese Recalled Due to Listeria Risk
Wegmans Food Markets recalled 4,884 units of Caramel Apple Pecan Topped Brie Cheese on August 12, 2025. The cheese may be contaminated with Listeria monocytogenes, a serious pathogen. Consumers should not consume this product and seek a refund.
Wegmans Food Markets
Products may
Health & Personal Care
HIGH
FDA DRUG
Viona Pharmaceuticals Recalls Tavaborole Topical Solution Over Discoloration Hazard
Viona Pharmaceuticals recalled 3,960 bottles of Tavaborole Topical Solution on August 12, 2025. The product may show discoloration, posing health risks to consumers. This recall affects topical solutions distributed nationwide in the USA.
TAVABOROLE
Discoloration
Food & Beverages
HIGH
FDA FOOD
H & N Group Recalls Frozen Shrimp Over Contamination Risk
H & N Group recalled 17,214 cases of frozen shrimp on August 12, 2025. The product may be contaminated with Cesium-137 due to unsanitary manufacturing conditions. Consumers should not consume the shrimp and seek refunds immediately.
H & N Group
Product manufactured
Health & Personal Care
HIGH
FDA DEVICE
Siemens Medical Solutions Recalls Fluoroscopic X-Ray System
Siemens Medical Solutions USA recalled 20 Artis Pheno. Image-Intensified Fluoroscopic X-Ray Systems due to limited system movements after startup. The recall, announced on August 12, 2025, affects devices distributed nationwide across several states.
Siemens Medical Solutions USA
Limited system
Food & Beverages
HIGH
FDA FOOD
Domino Foods Recalls Granulated Sugar Due to Contamination Risk
Domino Foods, Inc. recalled 4,500 bags of granulated sugar on August 12, 2025. The recall stems from potential contamination with foreign objects. The affected products were distributed in California and Utah.
Domino Foods
Potential contamination
Food & Beverages
HIGH
FDA FOOD
Wegmans Grilling Camembert Recalled Due to Listeria Risk
Wegmans Food Markets recalled 4,884 units of Grilling Camembert on August 12, 2025, due to possible contamination with Listeria monocytogenes. The affected products are packaged in black and gold metal trays and distributed in several states including New York and Pennsylvania. Consumers should not consume this product and seek a refund or replacement.
Wegmans Food Markets
Products may
Food & Beverages
HIGH
FDA FOOD
Baker's Authority Graham Cracker Meal Recalled Over Allergen Risks
Baker's Authority recalled 70 units of Graham Cracker Meal on August 12, 2025, due to undeclared allergens. The product lacks proper labeling for wheat and soy, posing a serious health risk to allergic consumers. These items were distributed across multiple states including NY, CA, and TX.
Bakers Authority
Product label
Health & Personal Care
HIGH
FDA DEVICE
Max Mobility Recalls Smart Drive MX2+ Dial Over Control Loss Risk
Max Mobility recalled 25,389 Smart Drive MX2+ SpeedControl Dials on August 12, 2025. A faulty electrical connection can lead to loss of control, posing injury risks. Users must stop using the device immediately and follow recall instructions.
Max Mobility
Due to
Food & Beverages
HIGH
FDA FOOD
Baker's Authority Seed Mix Recalled for Undeclared Allergen Risk
Baker's Authority recalled 78 units of Three Seed Mix on August 12, 2025. The product lacks proper labeling for sesame, a major allergen. Consumers should not consume this product and seek a refund.
Bakers Authority
Product label
Health & Personal Care
HIGH
FDA DEVICE
Applied Medical Technology Recalls Nasal Feeding Tubes Due to Detachment Hazard
Applied Medical Technology recalled 1,780 NutraGlide Nasal Feeding Tubes on August 12, 2025, after reports of distal tips detaching. This recall affects tubes distributed in Massachusetts and Rhode Island. The detachment poses a high risk for patients requiring enteral nutrition.
Applied Medical Technology
The nasal
Health & Personal Care
HIGH
FDA DEVICE
Applied Medical Technology Recalls NutraGlide Nasal Feeding Tubes Due to Detachment Risk
Applied Medical Technology recalled 200 NutraGlide Nasal Feeding Tubes on August 12, 2025. The distal tips may detach under lower than expected forces, posing a risk to patients. This recall affects devices distributed in Massachusetts and Rhode Island.
Applied Medical Technology
The nasal
Health & Personal Care
HIGH
FDA DEVICE
Applied Medical Technology Recalls Nasal Feeding Tubes Over Detachment Risk
Applied Medical Technology recalled 390 NutraGlide Nasal Feeding Tubes on August 12, 2025, due to a risk of distal tips detaching. This recall affects models distributed in Massachusetts and Rhode Island. Patients and healthcare providers must stop using these devices immediately.
Applied Medical Technology
The nasal
Health & Personal Care
HIGH
FDA DEVICE
Applied Medical Technology Recalls Nasal Feeding Tube Due to Detachment Hazard
Applied Medical Technology recalled 840 NutraGlide Nasal Feeding Tubes on August 12, 2025. The tubes may have distal tips that detach unexpectedly, posing a risk to patients. Healthcare providers and patients must stop using the device immediately and follow recall instructions.
Applied Medical Technology
The nasal
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