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 1618116200 of 29,093 recalls

Medical DeviceJune 8, 2018· Bio-Rad Laboratories, Inc

Recalled Item: MRSASelect Recalled by Bio-Rad Laboratories, Inc Due to Abnormal coloration...

The Issue: Abnormal coloration of agar plates and the growth of non-characteristic MRSA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Bio-Rad Laboratories, Inc

Recalled Item: MRSASelect II Recalled by Bio-Rad Laboratories, Inc Due to Abnormal...

The Issue: Abnormal coloration of agar plates and the growth of non-characteristic MRSA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2018· GE Medical Systems, LLC

Recalled Item: GE Healthcare MRI Systems Recalled by GE Medical Systems, LLC Due to The...

The Issue: The latest on-site software version may not have been reinstalled at some...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2018· GE Medical Systems, LLC

Recalled Item: GE Healthcare MRI Systems Recalled by GE Medical Systems, LLC Due to The...

The Issue: The latest on-site software version may not have been reinstalled at some...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2018· GE Medical Systems, LLC

Recalled Item: GE Healthcare MRI Systems Recalled by GE Medical Systems, LLC Due to The...

The Issue: The latest on-site software version may not have been reinstalled at some...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2018· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...

The Issue: The firm has learned that some RayStation/RayPlan users have commissioned...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2018· GE Medical Systems, LLC

Recalled Item: Discovery MR750w Nuclear Magnetic Resonance Imaging System labeled as the...

The Issue: GE Medical Systems has discovered a small area on the bore surface of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2018· Tosoh Bioscience Inc

Recalled Item: G8 Automated HPLC Analyzer: HLC-723G8-ST Recalled by Tosoh Bioscience Inc...

The Issue: HbAE is known to interfere with the HbA1c assay on the current version of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Single Chamber Temporary External Pacemaker Recalled by Medtronic Inc.,...

The Issue: A subset of Medtronic Model 53401 Single Chamber External Pulse Generators...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2018· Fx Solutions

Recalled Item: Fx SOLUTIONS CENTERED HEAD CoCr 50x19 Recalled by Fx Solutions Due to Breach...

The Issue: Breach in the external blister of certain lots of Humelock Offset Head 50 X...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2018· Richard-Allan Scientific Company

Recalled Item: EZ Single Cytofunnel Brown Recalled by Richard-Allan Scientific Company Due...

The Issue: Mislabeled product

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

Class III — Low RiskOngoing
Medical DeviceJune 4, 2018· Intuitive Surgical, Inc.

Recalled Item: EndoWrist Suction Irrigator Recalled by Intuitive Surgical, Inc. Due to The...

The Issue: The firm has identified the potential for a silicone particle to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2018· Neomed Inc

Recalled Item: NeoMed Enteral Feeding Tubes with Enteral Only Connectors Recalled by Neomed...

The Issue: Potential for the tethered plug on the hub of the NeoMed Enteral Feeding...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2018· Leica Microsystems, Inc.

Recalled Item: Leica Microsystems products labeled as the following: Leica M320 Microscope...

The Issue: Possible failure of screws which hold the gas spring fixation bracket in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2018· Fx Solutions

Recalled Item: Fx SOLUTIONS OFFSET HEAD CoCr 50x20 Recalled by Fx Solutions Due to Breach...

The Issue: Breach in the external blister of certain lots of Humelock Offset Head 50 X...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2018· B. Braun Medical, Inc.

Recalled Item: 26-Lead Transfer Set for use with APEX¿ Compounding System Recalled by B....

The Issue: There is a potential for valves on the 26-Lead Transfer Set to be...

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

Class II — Potential Health HazardOngoing