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. 2,366 recalls have been distributed to District of Columbia in the last 12 months.
Showing 45181–45200 of 47,654 recalls
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: Command Instrument Broach Handle. Used in Total Hip Arthroplasty. Catalog...
The Issue: Reports of handle fracture and subsequent disassociation of cam assembly...
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: HealthTronics Endocare 3.8mm RenalCryo Cryoprobe Recalled by Healthtronics,...
The Issue: The Endocare 3.8mm RenalCryo Cryoprobe is being recalled because the label...
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: 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.
Recalled Item: Medisystems 17 Gauge x 1" inch AV Fistula Needle Product Recalled by...
The Issue: Single needle packs in each case ( 10 needles per case) are mislabeled on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medisystems 15 Gauge x 3/5 inch Buttonhole Needle Set Product Recalled by...
The Issue: A total of 5 (ea) single needle pouches are mislabeled as 15 Ga x1" instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlowGate Balloon Guide Catheter Recalled by Concentric Medical Inc Due to...
The Issue: Firm received complaints of resistance and possible collapse of the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista (R) Urinary/Cerebrospinal Fluid Protein (UCFP) Flex (R)...
The Issue: Siemens has confirmed an increase on absorbance errors when calibrating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Synergy XVI. Radiation Therapy Digital Imager. Product XVI R3.5.1...
The Issue: The DICOM tags do not contain sufficient information for XVI to identify the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HAMILTON-T1 Ventilator with software versions 1.1.2 or lower. The HAMILTON...
The Issue: Analysis of a customer complaint has shown that during ventilation of small...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Taztia XT(diltiazem HCI extended release capsules Recalled by Watson...
The Issue: Failed Dissolution Specification: Out of a specification result occurred...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zicam Extreme Congestion Relief (oxymetazoline HCl) nasal gel Recalled by...
The Issue: Microbial Contamination of Non-Sterile Products: Product may be contaminated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Flanax (aluminum hydroxide Recalled by Belmora LLC Due to Defective...
The Issue: Defective Container: Product lacks tamper evident breakaway band on cap.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Surgical microscope The device is used to improve the visibility Recalled by...
The Issue: The brake in the Z axis and/or brakes in the AB and C axes failed during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical microscope The device is used to improve the visibility Recalled by...
The Issue: The brake in the Z axis and/or brakes in the AB and C axes failed during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...
The Issue: Small holes (approximately 1 mm or less) found in device unit level...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.