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. 1,099 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
1,099 in last 12 months

Showing 11961–11980 of 29,093 recalls

Medical DeviceApril 30, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Multi Display Manager in the Artis Systems (Image-Intensified Fluoroscopic...

The Issue: Artis systems containing a Multi Display Manager of a specific lot, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2020· GE Healthcare, LLC

Recalled Item: Giraffe OmniBed with installed Servo Oxygen module. Infant incubator and...

The Issue: Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2020· GE Healthcare, LLC

Recalled Item: Giraffe Incubator with installed Servo Oxygen module. Infant incubator....

The Issue: Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2020· Defibtech, LLC

Recalled Item: DDU-2450 Lifeline ECG Model Numbers DDU-A2450EN DDU-E2450DE DDU-E2450EN...

The Issue: A component issue may cause the AED to abort a shock delivery or reset...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2020· Defibtech, LLC

Recalled Item: DDU-2300 Lifeline/ReviveR View Recalled by Defibtech, LLC Due to A component...

The Issue: A component issue may cause the AED to abort a shock delivery or reset...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2020· Philips North America, LLC

Recalled Item: Philips HeartStart MRx Monitor/Defibrillators Model numbers M3535A Recalled...

The Issue: HeartStart XL MonitorlDefibrillators may not have been included in prior...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2020· Defibtech, LLC

Recalled Item: DDU-2400EN Lifeline PRO Recalled by Defibtech, LLC Due to A component issue...

The Issue: A component issue may cause the AED to abort a shock delivery or reset...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· Medtronic Sofamor Danek USA Inc

Recalled Item: Extremities Recalled by Medtronic Sofamor Danek USA Inc Due to Product may...

The Issue: Product may not maintain its setting characteristics for the labeled...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic Bone Void Filler Recalled by Medtronic Sofamor Danek USA Inc Due...

The Issue: Product may not maintain its setting characteristics for the labeled...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY ASY STR CONN 3/8 STRLE 24 Recalled by...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: 1/4X3/16X3/16YCONN Recalled by LivaNova USA Inc. Due to The firm has...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY Y CONN 1/4 X 1/4 X Recalled by LivaNova...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY S/1/4 TO 3/16 RED 24 REF/ Recalled by...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY 3/16 X 3/16 STR CONNW/LL24. REF/ Recalled...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY CONN REDUCER 1/2 X 3/8 24 Recalled by...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY CONN REDUCER 3/8 X 1/4 24 Recalled by...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: 3/8 STR CONN Recalled by LivaNova USA Inc. Due to The firm has identified...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: 1/4X3/8 REDUC CONN Recalled by LivaNova USA Inc. Due to The firm has...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: 1/2 - 3/8 REDUC CONN Recalled by LivaNova USA Inc. Due to The firm has...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Vein Irrigation Cannula with blunt tip. ASY BIC Recalled by LivaNova USA...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing