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
Drug Recalls Center
2,090 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.
2,090
Total Drug Recalls
24
High Risk Medications
FDA
Official Source
Important Medication Safety Information
- Do not stop taking prescribed medications without consulting your healthcare provider
- Contact your pharmacist or doctor if you have a recalled medication
- Check lot numbers carefully - not all batches may be affected
- Return recalled medications to your pharmacy for proper disposal
Looking for a specific drug? Use the search page to find recalls by medication name, manufacturer, or NDC number.
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 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 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 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
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 Penner Pacific Bathing Spa Recalled for Missing UDI (158 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
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 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
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 DRUG
Viona Pharmaceuticals Recalls Tavaborole Topical Solution 5% Over Discoloration (2025)
TAVABOROLE
Discoloration
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 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
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 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
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 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 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 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
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 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
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