Product Recalls in Maine

Product recalls affecting Maine — including food, drugs, consumer products, medical devices, and vehicles distributed to Maine. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,602 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
1,602 in last 12 months

Showing 45414560 of 27,655 recalls

Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion STERILE BLOOD COLLECTION TUBE Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion STERILE #5 LARYNGEAL MIRROR(505709) Recalled by MEDLINE...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion manual surgical kits labeled as: a) STERILE ALLIS TISS FCP 10"...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Centurion hook kits labeled as: a) STERILE SKIN HOOK FINE (EA3975F) Recalled...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· Agfa N.V.

Recalled Item: Agfa DX-D 100 system-Digital Radiography mobile X-ray System. A mobile...

The Issue: Steel cable installed inside the mobile column which supports the weight of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE SWABSTICKS ALCOHOL 3PK Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON Redwood 1.0 Diagnostic Ultrasound System Recalled by Siemens Medical...

The Issue: On ultrasound systems, when Cardiac DICOM SR feature is configured to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· Human Care Hc Sweden Ab

Recalled Item: Altair 330 lbs w/o Hanger Bar Recalled by Human Care Hc Sweden Ab Due to...

The Issue: Patient lift hanger bar may come loose, which could potentially pose risks...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation Auxiliary ES . Intended to securely Recalled by...

The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation ES (Med ES Main) . Intended Recalled by CareFusion 303,...

The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· Magellan Diagnostics, Inc.

Recalled Item: The LeadCare¿ II Blood Lead Test System relies on electrochemistry Recalled...

The Issue: Calibration Buttons being used in the kitting process were incorrectly...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON Juniper Diagnostic Ultrasound System Recalled by Siemens Medical...

The Issue: On ultrasound systems, when Cardiac DICOM SR feature is configured to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON Maple Diagnostic Ultrasound System Recalled by Siemens Medical...

The Issue: On ultrasound systems, when Cardiac DICOM SR feature is configured to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE SWABSTICKS PVP 3 PK Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Product may have a weak seal which may result in a breach of sterility of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation Auxiliary 4000 . Intended to securely Recalled by...

The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation 4000 . Intended to securely store Recalled by CareFusion...

The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2024· Baxter Healthcare Corporation

Recalled Item: Surgical Tools and Cardiovascular Specialty marketing brochures Recalled by...

The Issue: The Surgical Tools and Cardiovascular Specialty marketing brochures...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2024· Baxter Healthcare Corporation

Recalled Item: Surgical Tools and Cardiovascular Specialty marketing brochures Recalled by...

The Issue: The Surgical Tools and Cardiovascular Specialty marketing brochures...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2024· Baxter Healthcare Corporation

Recalled Item: Surgical Tools and Cardiovascular Specialty marketing brochures Recalled by...

The Issue: The Surgical Tools and Cardiovascular Specialty marketing brochures...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2024· Bolton Medical Inc.

Recalled Item: RELAY PRO Thoracic Stent-Graft System Recalled by Bolton Medical Inc. Due to...

The Issue: The stent-graft inside the delivery system was the incorrect size.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing