Product Recalls in Maryland

Product recalls affecting Maryland — including food, drugs, consumer products, medical devices, and vehicles distributed to Maryland. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,825 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,825 in last 12 months

Showing 1182111840 of 29,093 recalls

Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 8B Recalled by RAYSEARCH LABORATORIES AB Due to Software error...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 8A Service Pack 1 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 8A Recalled by RAYSEARCH LABORATORIES AB Due to Software error...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 4.0 to RayStation 5 Service Pack 2 - Product Recalled by...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 8B Service Pack 2 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 5 Service Pack 3 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 6 Service Pack 3 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· Carefusion 2200 Inc

Recalled Item: Mueller Knife Handle Recalled by Carefusion 2200 Inc Due to Becton Dickinson...

The Issue: Becton Dickinson and Company, is conducting a voluntary recall on the V....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 7 Recalled by RAYSEARCH LABORATORIES AB Due to Software error was...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 9A Recalled by RAYSEARCH LABORATORIES AB Due to Software error...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 9B Service Pack 1 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 8B Service Pack 1 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 6 Service Pack 2 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 6 Recalled by RAYSEARCH LABORATORIES AB Due to Software error was...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: (1) Atellica Data Manager software version 1.0 Siemens Material Number...

The Issue: Unexpected interface driver behavior identified (QC) Results May Be Assigned...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: PHANTOM CS DISTRACTION SCREW Recalled by TeDan Surgical Innovations LLC Due...

The Issue: Lack of pouch seal. Product is labelled as sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: PHANTOM CS QUICK START DISTRACTION SCREW Recalled by TeDan Surgical...

The Issue: Lack of pouch seal. Product is labelled as sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: (1) CentraLink Data Management System software version 16.0.2 Siemens...

The Issue: Unexpected interface driver behavior identified (QC) Results May Be Assigned...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· Mediana Co., Ltd.

Recalled Item: DIRECT SUPPLY Attendant VITAL SIGNS MONITOR Recalled by Mediana Co., Ltd....

The Issue: Failures were found in the temperature measurement function while in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2020· TeDan Surgical Innovations LLC

Recalled Item: PHANTOM CS QUICK START DISTRACTION SCREW Recalled by TeDan Surgical...

The Issue: Lack of pouch seal. Product is labelled as sterile.

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

Class II — Potential Health HazardOngoing