Product Recalls in District of Columbia
Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,485 recalls have been distributed to District of Columbia in the last 12 months.
Showing 22181–22200 of 47,654 recalls
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: Zimmer Biomet Alvarado Knee Holder Base Plate Assembly and Foot Piece...
The Issue: Foreign Material in the Alvarado Knee Holder Base Plate Assembly and Foot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIVCO Solstice(TM) SRS Immobilization System Recalled by Med Tec Inc Due to...
The Issue: There is a potential for movement of the Solstice Tilting Head Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity c Cuvette Segments Recalled by Abbott Gmbh & Co. KG Due to...
The Issue: Individual cuvettes within the Alinity c Cuvette Segment may become seated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.