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. 2,445 recalls have been distributed to District of Columbia in the last 12 months.
Showing 33041–33060 of 47,654 recalls
Recalled Item: Henry Schein Single Use Syringe Luer-Lock Recalled by Becton Dickinson &...
The Issue: BD 10 mL Syringe Luer-Lok Tip with BD PrecisionGlide Needle 21G x 1 (0.8 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuroBlate System SideFire Select 2.2 mm Directional Laser Probe Recalled by...
The Issue: Monteris received a report that the sapphire lens on a 2.2SF probe fractured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magellan Robotic Catheter Accessory Kits Recalled by Hansen Medical Inc Due...
The Issue: Firm's quarterly dose audit testing showed that one batch was radiated below...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoWrist Stapler 45 and Stapler 30 instruments used on the Recalled by...
The Issue: Potential for unexpected motion of the Xi Stapler jaws on the da Vinci Xi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Escitalopram Tablets USP 20 mg Recalled by Lupin Limited Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Lot and/or Expiration Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zemplar (paricalcitol) capsules Recalled by AbbVie Inc. Due to Failed...
The Issue: Failed Content Uniformity Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Weck EFx Classic Fascial Closure System Recalled by Teleflex Medical Due to...
The Issue: Incorrect expiration date was printed on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 16 Computed Tomography X-ray systems is intended to produce...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance BigBore Oncology Computed Tomography X-ray systems Recalled by...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 Computed Tomography X-ray systems is intended to Recalled...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance BigBore Radiology Computed Tomography X-ray systems Recalled by...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 Computed Tomography X-ray systems is intended to produce...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT 16 Power Computed Tomography X-ray systems is intended...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Computed Tomography X-ray systems is intended to produce...
The Issue: Software defect causing intermittently slow response of Host.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 500 Intelligent Lab System running on software versions...
The Issue: Discrepant patient results on Dimension Vista Intelligent Lab Systems....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 1500 Intelligent Lab System running on software versions...
The Issue: Discrepant patient results on Dimension Vista Intelligent Lab Systems....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit Recalled by CareFusion 303, Inc. Due to The Alaris PC units...
The Issue: The Alaris PC units model 8015 may display a system error code 133.6080 due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CELL-DYN Emerald Cleaner Recalled by Abbott Laboratories Due to Three lots...
The Issue: Three lots of CELL-DYN Emerald Cleaner may have occurrences where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magnesium Sulfate Inj. Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: Confirmed customer complaint for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chlorhexidine gluconate Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: Out-of-specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.