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. 1,912 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
1,912 in last 12 months

Showing 2424124260 of 52,535 recalls

Medical DeviceApril 17, 2019· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: AngioDynamics Solero Microwave Tissue Ablation (MTA) System: Solero...

The Issue: Updated Warning Statements in the Operator's Manual/Directions for Use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1) Solero...

The Issue: Updated Warning Statements in the Operator's Manual/Directions for Use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1) Solero...

The Issue: Updated Warning Statements in the Operator's Manual/Directions for Use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1)Solero...

The Issue: Updated Warning Statements in the Operator's Manual/Directions for Use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1)Solero...

The Issue: Updated Warning Statements in the Operator's Manual/Directions for Use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2019· Ad-Tech Medical Instrument Corporation

Recalled Item: AD-TECH Spencer Probe Depth Electrode Product Usage: The Ad-Tech Depth...

The Issue: An Ad-Tech Clinical Specialist, attended a case on April 15, 2019. During...

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

Class II — Potential Health HazardOngoing