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. 2,787 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,787 in last 12 months

Showing 1660116620 of 29,093 recalls

Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: Straight Plate Recalled by Orthofix, Inc Due to Firm is conducting a...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: MTP Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: CC Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: Locking Screw Recalled by Orthofix, Inc Due to Firm is conducting a...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: TN Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: L-Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: Rival View Kit Locking and Non-Locking Screw D 2.7MM Recalled by Orthofix,...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: H-Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: Rival Reduce Kit Locking and Non-Locking Screw D 2.0MM Recalled by Orthofix,...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: Box Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: Lapidus Plate Recalled by Orthofix, Inc Due to Firm is conducting a...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· Orthofix, Inc

Recalled Item: Y-Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...

The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2018· Visaris DOO

Recalled Item: Visaris Vision/Auto Recalled by Visaris DOO Due to A failure of the tube arm...

The Issue: A failure of the tube arm suspension is possible while the tube arm height...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2018· Visaris DOO

Recalled Item: Visaris Vision/Auto Recalled by Visaris DOO Due to A failure of the tube arm...

The Issue: A failure of the tube arm suspension is possible while the tube arm height...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2018· Visaris DOO

Recalled Item: Visaris Vision/Auto Recalled by Visaris DOO Due to A failure of the tube arm...

The Issue: A failure of the tube arm suspension is possible while the tube arm height...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2018· Abbott

Recalled Item: Thoratec HeartMate 3 LVAS Implant Kit Recalled by Abbott Due to Reports of...

The Issue: Reports of outflow graft twist occlusions. Patients whose devices experience...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 4, 2018· Handpiece Headquarters

Recalled Item: Henry Schein CU 1000 Halogen Curing Light Recalled by Handpiece Headquarters...

The Issue: Tip of the curing light was too hot causing a heat sensation in the patients.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2018· Deerfield Imaging, Inc.

Recalled Item: IMRIS IMRI 1.5T AND 3T S System Product Usage: The Recalled by Deerfield...

The Issue: The DC power to the IFOSS collision detector control panel at your facility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2018· Menarini Silicon Biosystems

Recalled Item: CELLSEARCH¿ CIRCULATING Tumor Cell Kits (IVD) (Product Code 7900001)...

The Issue: Unusually high number of total images/unassigned events may require...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version...

The Issue: Service technician improperly documented final release testing on product,...

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

Class II — Potential Health HazardOngoing