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. 2,542 recalls have been distributed to District of Columbia in the last 12 months.
Showing 16521–16540 of 27,451 recalls
Recalled Item: IntelliVue Multi Measurement Server Recalled by Philips Electronics North...
The Issue: Distorted ST-Segment when using 12-Lead ECG Monitoring with Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza systems with SW VB20A Recalled by Siemens Medical Solutions USA,...
The Issue: When a prior study is being replaced in the workflow step, in certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Recalled by Smiths Medical ASD Inc. Due to Potential for the...
The Issue: Potential for the syringe barrel clamp mechanism to loosen, decreasing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Recalled by Smiths Medical ASD Inc. Due to Potential for the...
The Issue: Potential for the syringe barrel clamp mechanism to loosen, decreasing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUIOS CL Flow Cytometer System The AQUIOS CL Flow Cytometer Recalled by...
The Issue: Beckman Coulter has identified that an incorrect setting using a proprietary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza Picture Archiving and Communication System (PACS) with software...
The Issue: Software update to correct several issues that include (1)Potential data...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TCC-EZ Recalled by Integra LifeSciences Corp. Due to A quarantined lot of...
The Issue: A quarantined lot of the devices was released for sale. Devices from this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A20975A "Working insert Recalled by Olympus Corporation of the Americas Due...
The Issue: Olympus has received complaints about fragments of adhesive which detached...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xper Flex Cardio Physiomonitoring system. Used to facilitate invasive...
The Issue: Intermittent communication between the host system and the FlexCardio
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 3 M12 Recalled by Philips Electronics North America Corporation Due...
The Issue: When using the downscale option with the Allura R9 system or Azurion R1.1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Unity software Recalled by Merge Healthcare, Inc. Due to The software...
The Issue: The software is not identifying the patient as having atypical hyperplasia,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Immunoassay Premium Plus Controls (3x4x5mL and 12x5mL packages) Recalled by...
The Issue: The ACTH in Immunoassay Premium and Premium Plus quality control does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Immunoassay Premium Controls (3x4x5mL and 12x5mL packages) Recalled by...
The Issue: The ACTH in Immunoassay Premium and Premium Plus quality control does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NS357R Vega PS Tibia Trial/Preparation Plateau size T4 (Component of...
The Issue: The NS357R Vega PS Tibia Trial/Preparation Plateau size T4 may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oncentra Brachy 4.5 radiation therapy software The firm name on Recalled by...
The Issue: Incorrect source step size may occur in the software plans
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norian Drillable Inject Recalled by Synthes USA Due to The contract supplier...
The Issue: The contract supplier notified DePuy Synthes on June 16, 2017 that the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transfer/Gait Belt Recalled by Medline Industries Inc Due to The locking...
The Issue: The locking mechanism on the belt may fail to secure/hold the strap when in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transfer/Gait Belt Recalled by Medline Industries Inc Due to The locking...
The Issue: The locking mechanism on the belt may fail to secure/hold the strap when in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norian Drillable Inject Recalled by Synthes USA Due to The contract supplier...
The Issue: The contract supplier notified DePuy Synthes on June 16, 2017 that the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Module model 8100 manufactured between November 2011 and March...
The Issue: The recalling firm has received reports of increased or decreased flows that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.