stop use immediately Recalls

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 Recalls 15 Penner Pacific Bathing Spa Devices for Missing UDI (2025)

The device does not bear a unique device identifier.

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 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.

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.

Siemens Artis Pheno Fluoroscopic X-Ray System Recalled for 20 Units in 2025

Limited system movements after startup .

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.

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)

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.

Viona Pharmaceuticals Recalls Tavaborole Topical Solution 5% Over Discoloration (2025)

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

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 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 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 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.

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 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 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.

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.

Baxter Continu-Flo Intravascular Set Recalled for Tubing Separation — 14,400 Units in 2025

Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for one lot of Continu-Flo solution sets listed below due to customer reports of tubing separation.