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 25921–25940 of 27,451 recalls
Recalled Item: Stryker XIA 3 Iliac Screwdriver Recalled by Stryker Spine Due to Surgeons...
The Issue: Surgeons have experienced unthreading of the screwdrivers outer shafts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraClean(R) Accessory Electrode 1 inch Coated Needle with Extended...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELECTROLASE(R) HYFRECATOR(R) ELECTRODES - SHARP Recalled by ConMed...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraClean(R) Accessory Electrode Recalled by ConMed Corporation Due to...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraClean(R) Accessory Electrode 6 inch Coated Blade Recalled by ConMed...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONMED(R) ELECTROSURGICAL SAFETY HOLSTER Recalled by ConMed Corporation Due...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELECTROLASE(R) HYFRECATOR(R) ELECTRODES - BLUNT Recalled by ConMed...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABC(R) NOZZLE Recalled by ConMed Corporation Due to ConMed received...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELECTROSURGICAL ENT NEEDLE ELECTRODE Recalled by ConMed Corporation Due to...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device)...
The Issue: HeartWare, Inc. of Miami Lakes, FL is recalling their Ventricular Assist...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraClean(R) Accessory Electrode 4 inch Coated Blade with Extended...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Goldvac(TM) UltraClean(R) Accessory Electrode 6 inch Coated Blade with...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1-DAY ACUVUE MOIST Brand Contact Lenses Recalled by Johnson & Johnson Vision...
The Issue: Limited number of individual contact lens packages may not have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR Recalled by Johnson &...
The Issue: Limited number of individual contact lens packages may not have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: nordicBrainEX Product Usage: nordicBrainEx is an image processing software...
The Issue: There is an error related to the relative geometry between fiber tracts in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion SmartSite Gravity Blood Set Model 42082E. Used to administer...
The Issue: CareFusion is recalling the SmartSite¿ Gravity Blood Set as a result of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO Sensar Intraocular Lenses (IOLs) Recalled by Abbott Medical Optics Inc...
The Issue: Two production orders of these IOLs that contain mislabeled IOLs.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Total Iron Binding Capacity (IBCT) Flex Reagent Cartridge. An...
The Issue: The analytical sensitivity claim of 6 ug/dL (1.1 umol/L) in the Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 6 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: Philips Healthcare received reports from the field stating the patient table...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension(R) IRON Calibrator (DC85) Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics has received complaints of IRON calibrations...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.