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. 2,629 recalls have been distributed to District of Columbia in the last 12 months.
Showing 5721–5740 of 27,451 recalls
Recalled Item: Visera Hysterovideoscope Olympus HYF Type V Recalled by Olympus Corporation...
The Issue: IFU labeling is being updated to revise EtO gas mixture and elimination of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHOROPTOR VRX DIGITAL SYSTEM-Digital intended for the subjective Recalled by...
The Issue: Phoroptor VRx Head may detach from the bracket that connects the Phoroptor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOxBOXi Nitric Oxide Delivery System Recalled by NOXBOX LTD Due to...
The Issue: Replacement of the internal Sample Pump due to high failure rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper series Recalled by Philips Medical Systems Nederland B.V. Due to...
The Issue: A foot switch pedal may get stuck in the active position when the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion Recalled by Philips Medical Systems Nederland B.V. Due to A foot...
The Issue: A foot switch pedal may get stuck in the active position when the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDiagnost-Eleva Recalled by Philips Medical Systems Nederland B.V. Due...
The Issue: A foot switch pedal may get stuck in the active position when the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim" XR 7 Implantable Pulse Generator (previously known Recalled by...
The Issue: Firm has received complaints from patients who are unable to exit MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim Plus 5 Implantable Pulse Generator Product Description: Recalled by...
The Issue: Firm has received complaints from patients who are unable to exit MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim XR 5 Implantable Pulse Genterator (previously known Recalled by...
The Issue: Firm has received complaints from patients who are unable to exit MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity 5 Implantable Pulse Generator Product Description: The Recalled by...
The Issue: Firm has received complaints from patients who are unable to exit MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity 7 Implantable Pulse Generator Product Description: The Recalled by...
The Issue: Firm has received complaints from patients who are unable to exit MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim DRG Implantable Pulse Generator Product Description: The Recalled...
The Issue: Firm has received complaints from patients who are unable to exit MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim Plus 7 Implantable Pulse Generator Product Description: Recalled by...
The Issue: Firm has received complaints from patients who are unable to exit MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PORTEX 0.5u HYDROPHOBIC DISC FILTER Recalled by Smiths Medical ASD Inc. Due...
The Issue: Smiths Medical identified a labeling error in which the barcode (UDI) was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquilex Fluid Control System-Intended to provide fluid distension of the...
The Issue: The display of inflow volume can reach its limit of 30,000 ml during long...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayCare software Recalled by RAYSEARCH LABORATORIES AB Due to An issue was...
The Issue: An issue was found in Software RayCare 5A, 5B, 6A, including service packs,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L-Aneurysm Clip TITANIUM Paddle-Clip Recalled by Peter Lazic Gmbh Due to...
The Issue: Wrong product coloring. The paddle clips should be blank, but they are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L-Aneurysm Clip TITANIUM Paddle-Clip Recalled by Peter Lazic Gmbh Due to...
The Issue: Wrong product coloring. The paddle clips should be blank, but they are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Embrace2- Indicated for use as an adjunct to seizure monitoring Recalled by...
The Issue: May have a battery life lasting less than the full 48 hours, requiring the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP Family 50 Series Models as follows: In vitro Recalled by...
The Issue: Sample misidentification could occur under specific conditions and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.