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. 2,584 recalls have been distributed to District of Columbia in the last 12 months.
Showing 12181–12200 of 27,451 recalls
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: Spy-Phi Drape (HH2000) sold as a Spy-Phi Pack (HH9006). Only Recalled by...
The Issue: Sterile drapes packaged in an unsealed pouch.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spy-Phi Drape only (HH2020) Pack of 20 HH2000 (Sold internationally Recalled...
The Issue: Sterile drapes packaged in an unsealed pouch.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America BodyGuard Infusion Pump System Recalled by CME America, LLC Due...
The Issue: Infusion Pump Systems may have a delivery inaccuracy of up to 13%, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cocoon Convective Warming System Recalled by Care Essentials Pty., Ltd. Due...
The Issue: Potential for thermal damage near the power cord connector and Power Entry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cocoon Convective Warming System Recalled by Care Essentials Pty., Ltd. Due...
The Issue: Potential for thermal damage near the power cord connector and Power Entry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Humidity Pack (Qty 5) Recalled by Siemens Healthcare...
The Issue: A software error is causing the analyzer to incorrectly eject affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Humidity Pack (Qty 1) Recalled by Siemens Healthcare...
The Issue: A software error is causing the analyzer to incorrectly eject affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA Brain 3.0 Application-Brain Recalled by MEDTECH SAS Due to Some...
The Issue: Some cross-sectional images from the image acquisitions of the patients head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA One 3.1 Brain Application Recalled by MEDTECH SAS Due to Some...
The Issue: Some cross-sectional images from the image acquisitions of the patients head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...
The Issue: Lot numbers and products inadvertently not included in the scope of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...
The Issue: Lot numbers and products inadvertently not included in the scope of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...
The Issue: Lot numbers and products inadvertently not included in the scope of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...
The Issue: Lot numbers and products inadvertently not included in the scope of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.