Health & Personal Care Recalls

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

Limited system movements after startup .

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/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 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.

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 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 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 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.

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 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 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.

Glenmark Theophylline Extended-Release 400mg Recall Expanded for Failed Dissolution Tests (2025)

Quallent Pharmaceuticals Health LLC Recall Expands for Duloxetine Delayed-Release Capsules Over Imp-

CGMP deviations: N-nitroso-duloxetine impurity above the proposed interim limit.

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.

PHILIPS IntelliSpace Cardiovascular Software 8.0.0.4 Recall Affects 4 Units Nationwide

Software issue that results in the display of outdated information.

Schiller Argus PB-3000 Vital Signs Monitor Recall Affects 266 US Units

Vital sign monitoring instrument may trigger an error message during blood pressures measurements, Specifically, when the initial inflation pressure is set in the high-pressure range.

Medline Medline Extremity Pack DYNJ45701B Sterile Kit Recall Affects 88 Units (2025)

Convenience kits labeled as sterile have not gone through the sterilization process.

Medline Industries Recalls 22 Sterile Convenience Kits DYNJ0382730O, DYNJ61038B (2025)

Convenience kits labeled as sterile have not gone through the sterilization process.

Séfralls Minoxidil Hair Generation Serum Recalled for Child Poisoning Risk (2025)

This recall involves Séfralls Hair Generation Serum. The hair serum comes in an amber dropper bottle with a white and gold dropper and a white, black and gold label. "Séfralls" and "Minoxidil" are printed on the label located on the front of the bottle.