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 5501–5520 of 27,451 recalls
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sapphire Infusion Pumps Recalled by EITAN MEDICAL LTD Due to Infusion Pumps...
The Issue: Infusion Pumps with affected software revision may fail to detect air in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Viewer Workflow Manager Recalled by GE Healthcare Due to When...
The Issue: When using Universal Viewer or Centricity Universal Viewer with Workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer Workflow Manager Recalled by GE Healthcare Due...
The Issue: When using Universal Viewer or Centricity Universal Viewer with Workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: F2-01 Frame Recalled by GE Medical Systems China Co., Ltd. Due to There is a...
The Issue: There is a potential interruption of data communication between E-modules...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Real Intelligence CORI RI.KNEE v2.0 TKA (Total Knee Arthroplasty) software...
The Issue: CORI software was missing a planning stage that appears in cases of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AU/DxC AU Chemistry Transferrin Immune complexes formed in Recalled by...
The Issue: The firm has identified that the Transferrin reagent does not meet the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX Modena-IVD Clinical Chemistry Analyser Catalog Number: RX9000 Recalled by...
The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX Monaco-IVD Clinical Chemistry Analyser Catalog Number: RX5000 Recalled by...
The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX Imola-IVD Clinical Chemistry Analyzer Catalog Number: RX4900. RX4900R ()...
The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.