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. 1,090 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
1,090 in last 12 months

Showing 13781–13800 of 29,093 recalls

Medical DeviceJune 17, 2019· Datascope Corp.

Recalled Item: CS100 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...

The Issue: If battery maintenance is not performed appropriately, the battery may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2019· Datascope Corp.

Recalled Item: Cardiosave Rescue IABP Recalled by Datascope Corp. Due to If battery...

The Issue: If battery maintenance is not performed appropriately, the battery may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2019· Intuitive Surgical, Inc.

Recalled Item: da Vinci Surgical System Recalled by Intuitive Surgical, Inc. Due to One da...

The Issue: One da Vinci Xi Endoscope Controller in the field was improperly calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2019· Bard Peripheral Vascular Inc

Recalled Item: EQUISTREAM¿ XK Long-Term Hemodialysis Catheter....

The Issue: Incorrect Peel-Apart Introducer Sheath in Kit.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2019· Bard Peripheral Vascular Inc

Recalled Item: EQUISTREAM¿ XK Long-Term Hemodialysis Catheter....

The Issue: Incorrect Peel-Apart Introducer Sheath in Kit.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2019· TELEFLEX-MORRISVILLE

Recalled Item: Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 Recalled by...

The Issue: Device vented gas below the stated pressure.

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 14, 2019· Stanley Security Solutions Inc

Recalled Item: STANLEY Healthcare Arial 54315 Network Manager Recalled by Stanley Security...

The Issue: STANLEY Healthcare has received reports of outages on the Arial nurse call...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2019· SpineFrontier, Inc.

Recalled Item: A-CIFT SoloFuse Fixed Angle Driver Recalled by SpineFrontier, Inc. Due to...

The Issue: There is a potential for the driver to bind up when attempting to advance...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis dMP Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A tolerance issue in the power supply of the generator control above a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee floor MN Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A tolerance issue in the power supply of the generator control above a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2019· Becton Dickinson & Company

Recalled Item: BD Vacutainer PST Gel and Lithium HeparinN (LH) Blood Collection Tubes...

The Issue: False elevation of carboxyhemoglobin (COHb) results have been reported when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zeego Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A tolerance issue in the power supply of the generator control above a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee multi Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A tolerance issue in the power supply of the generator control above a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis dTA Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A tolerance issue in the power supply of the generator control above a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee floor Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A tolerance issue in the power supply of the generator control above a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis TA Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A tolerance issue in the power supply of the generator control above a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis dFC Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A tolerance issue in the power supply of the generator control above a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis BA Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A tolerance issue in the power supply of the generator control above a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis BC Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A tolerance issue in the power supply of the generator control above a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis FC Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A tolerance issue in the power supply of the generator control above a...

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

Class II — Potential Health HazardOngoing