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. 945 recalls have been distributed to Maryland in the last 12 months.
Showing 46741–46760 of 52,535 recalls
Recalled Item: Bella Vi INSANE Bee Pollen Dietary Supplement Capsules Recalled by Pure Edge...
The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bella Vi BTrim MAX Dietary Supplement capsules Recalled by Pure Edge...
The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bella Vi INSANE AMP'D Dietary Supplement capsules Recalled by Pure Edge...
The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bella Vi eXtreme ACCELERATOR Dietary Supplement Capsules Recalled by Pure...
The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bella Vi AMP'D UP Advanced Weight Loss Dietary Supplement capsules Recalled...
The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS Chemistry Products Mixing Cup Arrays utilized on VITROS 250 Recalled...
The Issue: Ortho Clinical Diagnostics issued a product correction notification for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Juggerknotless Drill Bit Recalled by Biomet, Inc. Due to Investigation...
The Issue: Investigation identified that the design of the drill bit may make the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Verigene Gram Negative Blood Culture Nucleic Acid Test (BC-GN) Recalled...
The Issue: Nanosphere has received several reports relating to an increased rate of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Verigene Gram-Positive Blood Culture Nucleic Acid Test (BC-UP) performed...
The Issue: Nanosphere has received several reports relating to an increased rate of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mizuho Sugita Titanium Standard Aneurysm Clip II Recalled by Mizuho America,...
The Issue: Specific item numbers form Lots 27-J and 29-J of Sugita T2 Aneurysm Clips....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mizuho Sugita Titanium Standard Aneurysm Clip II Recalled by Mizuho America,...
The Issue: Specific item numbers form Lots 27-J and 29-J of Sugita T2 Aneurysm Clips....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Verigene Enteric Pathogens Nucleic Acid Test (EP) is a multiplexed...
The Issue: Nanosphere has received several reports relating to an increased rate of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Verigene Respiratory Virus Plus Nucleic Acid Test (RV+) on Recalled by...
The Issue: Nanosphere has received several reports relating to an increased rate of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nova StatStrip/StatSensor Hospital Blood Glucose Meter Recalled by Nova...
The Issue: Revised Battery Instructions for Removal and Expiration Date due to battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Verigene Clostridium difficile Nucleic Acid Test (CDF) is a qualitative...
The Issue: Nanosphere has received several reports relating to an increased rate of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Optima CT520 and Optima CT540 Computed Tomography (CT) systems. Recalled...
The Issue: There is an issue with the Manual Film Composer feature on some CT products....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinica Anterior Lumbar Plate (ALP) system Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Spine, Inc. is initiating a correction regarding the Trinica ALP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes TomoFix Plates The Synthes J5606-C TomoFix Osteotomy System is...
The Issue: A labeling correction was initiated related to the Surgical Technique Guide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Transradial Artery Access products Arrow Transradial Artery Access...
The Issue: There is a risk that the introducer needles packaged within the kits can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS CA 125 II Calibrators For use in the calibration Recalled by...
The Issue: Ortho Clinical Diagnostics issued a Product Correction Notification for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.