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. 2,448 recalls have been distributed to District of Columbia in the last 12 months.
Showing 26321–26340 of 27,451 recalls
Recalled Item: CareStream Dental CS 2200 X-ray system Product Usage: The expected Recalled...
The Issue: There have been approximately 2% of the x-ray generators manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iris Diagnostics Division iQ Control/Focus Set Recalled by Iris Diagnostics...
The Issue: The firm initiated this recall because complaints from customers reported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareStream Dental Kodak 2200 Intraoral X-ray system Product Usage: The...
The Issue: There have been approximately 2% of the x-ray generators manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareStream Dental CS 2100 X-ray system Product Usage: The expected Recalled...
The Issue: There have been approximately 2% of the x-ray generators manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareStream Dental Kodak 2100 Intraoral X-ray system Product Usage: The...
The Issue: There have been approximately 2% of the x-ray generators manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrig Trigger Release Sterile Micro Hook Blade Product Usage: The...
The Issue: Instratek, Inc.has received multiple complaints of the 1052 Trigger Finger...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mx8000 IDT Whole Body Computed Tomography X-ray system Distributed by...
The Issue: The low contrast pins in the Image Quality (IQ) phantom deteriorates over...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ MOSAIQ is an image-enabled electronic medical record system (EMR)...
The Issue: A patient was seriously mistreated after a user made and saved an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDLab¿ 1265 system blood gas analyzer Product Usage: RAPIDLab...
The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDLab¿ 1260 system blood gas analyzer Product Usage: RAPIDLab...
The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDLab¿ 1245 system blood gas analyzer Product Usage: RAPIDLab...
The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDLab¿ 1240 system blood gas analyzer Product Usage: RAPIDLab...
The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDPoint¿ 400 system blood gas analyzer Product Usage: These...
The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDPoint¿ 500 system blood gas analyzer Product Usage: RAPIDPoint...
The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDPoint¿¿ 405 system blood gas analyzer Product PUsage: These...
The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BariAir Therapy System The BariAir Therapy System is a risk Recalled by KCI...
The Issue: KCI has issued a medical device correction for the BariAir Therapy System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS System versions 3.X and higher and 4.X and Recalled by Ge...
The Issue: There is a potential loss of image(s) associated with the Centricity to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hologic Fluoroscan Mini C-Arm Model with InSight2 Recalled by Hologic, Inc....
The Issue: InSight2, version 4.0 and 4.0.1 - DICOM images stored in PACS may be flipped...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy F/M Acetabular Shell without holes SOLID HA. Several ODs: 38MM...
The Issue: Some units of Trilogy shells manufactured since March 2009 may be below the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Acetabular Shell with Cluster Holes. The Trilogy Acetabular System...
The Issue: Some units of Trilogy shells manufactured since March 2009 may be below the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.