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. 2,529 recalls have been distributed to District of Columbia in the last 12 months.
Showing 19101–19120 of 47,654 recalls
Recalled Item: Terumo Advanced Perfusion Assembly Pump Guts Recalled by Terumo...
The Issue: These roller pumps were assembled with pump shafts that may fail at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1 Roller Pump Recalled by Terumo...
The Issue: These roller pumps were assembled with pump shafts that may fail at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion Assembly Pump Guts Recalled by Terumo...
The Issue: These roller pumps were assembled with pump shafts that may fail at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1 Roller Pump Recalled by Terumo...
The Issue: These roller pumps were assembled with pump shafts that may fail at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System...
The Issue: The products are being recalled due to reports of breakage broke at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System...
The Issue: The products are being recalled due to reports of breakage broke at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Healthineers Uroskop Omnia max Model: 10762473 - Product Usage:...
The Issue: Two software issues (1) Using the override function in case of blocked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Healthineers Ysio Max - Interventional Fluoroscopic X-Ray System...
The Issue: Two software issues (1) Using the override function in case of blocked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Healthineers Luminos Agile Max Model: 10762472 - Product Usage:...
The Issue: Two software issues (1) Using the override function in case of blocked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Healthineers Luminos dRF Max Model: 10762471- Product Usage: is...
The Issue: Two software issues (1) Using the override function in case of blocked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ysio Max Recalled by Siemens Medical Solutions USA, Inc Due to A software...
The Issue: A software bug may lead to one image to be assigned to two different...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos Agile Max Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Siemens became aware of an issue of incorrect use of the bypass key...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos Agile Max Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A software bug may lead to one image to be assigned to two different...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos dRF Max Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Siemens became aware of an issue of incorrect use of the bypass key...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminos dRF Max Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A software bug may lead to one image to be assigned to two different...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uroskop Omnia max Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Siemens became aware of an issue of incorrect use of the bypass key...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dutasteride Capsules Recalled by AVKARE Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: High out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Garlic Parmesan Sauce Recalled by Golden State Foods Due to Notification by...
The Issue: Notification by supplier of a recall of starch ingredient due to metal...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Taco Bell Creamy Jalapeno Sauce Recalled by Golden State Foods Due to...
The Issue: Notification by supplier of a recall of starch ingredient due to metal...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pizza Hut Garlic Dipping Sauce Recalled by Golden State Foods Due to...
The Issue: Notification by supplier of a recall of starch ingredient due to metal...
Recommended Action: Do not consume. Return to store for a refund or discard.