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. 2,636 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,636 in last 12 months

Showing 3714137160 of 52,535 recalls

DrugFebruary 16, 2016· Actavis Elizabeth LLC

Recalled Item: Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 16, 2016· Actavis Elizabeth LLC

Recalled Item: Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 16, 2016· Genzyme Corporation

Recalled Item: Thyrogen (thyrotropin alfa for injection) Recalled by Genzyme Corporation...

The Issue: Presence of Particulate Matter: Glass particles found in the product after...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 16, 2016· Genzyme Corporation

Recalled Item: Thyrogen (thyrotropin alfa for injection) Recalled by Genzyme Corporation...

The Issue: Presence of Particulate Matter: Glass particles found in the product after...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 16, 2016· Progressive Gourmet Inc.

Recalled Item: Sausage Recalled by Progressive Gourmet Inc. Due to Potential Listeria...

The Issue: Manufactured in a plant where routine environmental swabs tested positive...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 4.5 mm Cannulated Screw Recalled by Synthes (USA) Products LLC Due to...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 4.5 mm Cortex Screw Recalled by Synthes (USA) Products LLC Due to Labeling...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 6.5 mm Cannulated Screw Recalled by Synthes (USA) Products LLC Due to...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 7.0 mm and 7.3 mm Cannulated Screw Recalled by Synthes (USA) Products LLC...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 6.5 mm Cancellous Screw Recalled by Synthes (USA) Products LLC Due to...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 3.5 mm and 4.0 mm Cannulated Screw Recalled by Synthes (USA) Products LLC...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 4.0 mm Cortex Screw Recalled by Synthes (USA) Products LLC Due to Labeling...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Blood Urea Nitrogen (BUN) Flex reagent cartridge The...

The Issue: Siemens Healthcare Diagnostics has determined that Dimension Vista Blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: The two sets of wires (4 total wires) exiting from the EMI filters were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: CIOS ALPHA (Image-intensified fluoroscope x-ray system) Product Usage: The...

The Issue: Siemens found a defective part in their production line which could increase...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: Synthes Interlocking Bolt Recalled by Synthes (USA) Products LLC Due to...

The Issue: DePuy Synthes is initiating a voluntary medical device recall of certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Biomet, Inc.

Recalled Item: Verso Shoulder Forked Retractor (Comprehensive Instrumentation 2 Prong...

The Issue: Zimmer Biomet Inc. Verso Shoulder Forked Retractor (Comprehensive...

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

Class II — Potential Health HazardOngoing
FoodFebruary 15, 2016· Winter Gardens Quality Foods, Inc.

Recalled Item: Blue Ridge Farms Macaroni Salad Recalled by Winter Gardens Quality Foods,...

The Issue: The supplier of the salad oil used in the above product(s) has voluntarily...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 15, 2016· Winter Gardens Quality Foods, Inc.

Recalled Item: Blue Ridge Farms Potato Salad 01045 Recalled by Winter Gardens Quality...

The Issue: The supplier of the salad oil used in the above product(s) has voluntarily...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 15, 2016· Winter Gardens Quality Foods, Inc.

Recalled Item: Blue Ridge Farms Supreme Tuna Salad Recalled by Winter Gardens Quality...

The Issue: The supplier of the salad oil used in the above product(s) has voluntarily...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund