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. 2,648 recalls have been distributed to Maryland in the last 12 months.
Showing 34141–34160 of 52,535 recalls
Recalled Item: FlexLab Automation Modules Recalled by Siemens Healthcare Diagnostics, Inc....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Professional Hospital Supply Recalled by Covidien LLC Due to Added...
The Issue: Added Instructions for Use: After application, inspect the Light Glove for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Devon Light Glove packaged in sterile surgical kits : Recalled by...
The Issue: Added Instructions for Use: After application, inspect the Light Glove for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FindrWIRZ Guidewire System Catalog# 40-05 Cardiology: The system is intended...
The Issue: A complaint was received on September 27th, 2016 at a medical center in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Devon Light Glove sub-assembly non-sterile For Kit Packers Product...
The Issue: Added Instructions for Use: After application, inspect the Light Glove for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System The Monaco system is used to make Recalled by Elekta, Inc....
The Issue: When creating 3D plans using either MU or Dose weighting modes, if the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clonazepam Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...
The Issue: Failed Impurities/Degradation Specifications: out of specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clonazepam Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...
The Issue: Failed Impurities/Degradation Specifications: out of specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brownwood Farms Yankee Bourbon BBQ Sauce. 19oz glass bottles and 1 gallon...
The Issue: Products contain soy ingredients not declared on the label.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brownwood Farms Apple Riesling Salsa. 21oz glass bottles and 1 Recalled by...
The Issue: Products contain yellow#5 ingredients not declared on the label.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brownwood Farms BBQ Mustard Glaze. 11oz glass bottles and 1 Recalled by...
The Issue: Products contain soy ingredients not declared on the label.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brownwood Farms Jalapeno Cherry Butter. 12oz glass bottles and 1 gallon....
The Issue: Products contain yellow#5 ingredients not declared on the label.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brownwood Farms Jalapeno Cherry Salsa. 21oz glass bottles and 1 Recalled by...
The Issue: Products contain yellow#5 ingredients not declared on the label.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brownwood Farms Peach Salsa. 17oz glass bottles. Private labels: Bowers...
The Issue: Products contain yellow#5 ingredients not declared on the label.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brownwood Farms Cherry BBQ Sauce. 21oz glass bottles Recalled by Brownwood...
The Issue: Products contain soy ingredients not declared on the label.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...
The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...
The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5...
The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5...
The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5...
The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.