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 5281–5300 of 27,451 recalls
Recalled Item: Integra Cranial access kit (without Prep solutions) Bit and Guard-For...
The Issue: Defect in the outer packaging of the Cranial Access Kits can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial Access Kit-For access to the subarachnoid space or Recalled...
The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra¿ Cranial Access Kit-For access to the subarachnoid space or Recalled...
The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial Access Kit -For access to the subarachnoid space Recalled by...
The Issue: Defect in the outer packaging of the Cranial Access Kits can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial Access Kit-For access to the subarachnoid space or Recalled...
The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial Access Kit- For access to the subarachnoid space Recalled by...
The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra¿ Cranial Access Kit-For access to the subarachnoid space or Recalled...
The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Combo Kit Consists OF 10-110/INS-4500/INS-7040- For access to the...
The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Platform 100-240V- 50/60Hz 1440w Recalled by AURIS HEALTH INC Due to...
The Issue: Their is the potential that software issues may result in flipped image of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Platform Recalled by AURIS HEALTH INC Due to Their is the potential...
The Issue: Their is the potential that software issues may result in flipped image of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Platform Recalled by AURIS HEALTH INC Due to Their is the potential...
The Issue: Their is the potential that software issues may result in flipped image of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIKSTIK Recalled by Microbiologics Inc Due to A complaint investigation...
The Issue: A complaint investigation showed that the bulk pellets (lot 794-142) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LYFO-DISK Recalled by Microbiologics Inc Due to A complaint investigation...
The Issue: A complaint investigation showed that the bulk pellets (lot 794-142) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS icono (ceiling configuration) Recalled by Siemens Medical Solutions...
The Issue: Potential hardware issue for ARTIS icono ceiling system: collision sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFIRE Blood Culture Identification 2 (BCID2) Panel Recalled by BioFire...
The Issue: Routine quality control testing of affected blood culture identification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray TORCH . HTFA-ASY-0104 is the BIOFIRE TORCH Base Recalled by...
The Issue: Due to an increased risk of degradation of the power entry switch resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitality Polyaxial Screw Recalled by Zimmer Biomet Spine Inc. Due to Spinal...
The Issue: Spinal fixation system 7.5mmx 50mm screws are packaged with the correct...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tracheostomy care kits: (1) Medline Tracheostomy Clean and Care Tray...
The Issue: The component tracheostomy brush has a sharp edge at the tip that can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Nursing Skills kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: The component tracheostomy brush has a sharp edge at the tip that can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Nurse Kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to The...
The Issue: The component tracheostomy brush has a sharp edge at the tip that can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.