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. 2,565 recalls have been distributed to District of Columbia in the last 12 months.
Showing 15161–15180 of 47,654 recalls
Recalled Item: Toshiba Vantage Tiitan 1.5T with Standard gradient Recalled by Canon Medical...
The Issue: The MRI system contains a component that does not meet the appropriate flame...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon Vantage Tiitan 1.5T Recalled by Canon Medical System, USA, INC. Due to...
The Issue: The MRI system contains a component that does not meet the appropriate flame...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon Vantage Galan 3T Recalled by Canon Medical System, USA, INC. Due to...
The Issue: The MRI system contains a component that does not meet the appropriate flame...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nonsterile Sterile Cesarean Birth Drape with Dual Layer Anesthesia Screen...
The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Cesarean Birth Drape with Dual Layer Anesthesia Screen Recalled by...
The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Femoral Angiography Drape with Single Pouch Recalled by Cardinal...
The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nonsterile Femoral Angiography Drape Recalled by Cardinal Health 200, LLC...
The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nonsterile Femoral Angiography Drape with Single Pouch Recalled by Cardinal...
The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nonsterile Radial/Femoral Angiography Drape Recalled by Cardinal Health 200,...
The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Femoral Angiography Drape Recalled by Cardinal Health 200, LLC Due...
The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Radial/Femoral Angiography Drape Recalled by Cardinal Health 200,...
The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUNSTAR G.U.M PERIOSHIELD Oral Health Rinse Recalled by Sunstar Americas,...
The Issue: Products may be contaminated with micro-organisms Burkholderia cepacia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...
The Issue: Defective Delivery System: The number of customer complaints for ripping...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...
The Issue: Defective Delivery System: The number of customer complaints for ripping...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FREELITE Human Kappa Free Kit for use on the Roche cobas c Systems Recalled...
The Issue: The high and low level "Quality Controls" demonstrate a positive bias of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 High Performance. radiography and fluoroscopy system...
The Issue: Following a system restart where the Table Height 2 (TH2) is the default...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90. radiography and fluoroscopy system Recalled by Philips...
The Issue: Following a system restart where the Table Height 2 (TH2) is the default...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 High Performance. radiography and fluoroscopy system...
The Issue: Following a system restart where the Table Height 2 (TH2) is the default...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 Flex/Value/Chest/ER. radiography and fluoroscopy system...
The Issue: Following a system restart where the Table Height 2 (TH2) is the default...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 Flex / Value. radiography and fluoroscopy system Recalled...
The Issue: Following a system restart where the Table Height 2 (TH2) is the default...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.