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. 2,591 recalls have been distributed to District of Columbia in the last 12 months.
Showing 11381–11400 of 47,654 recalls
Recalled Item: Artis icono biplane- Model No. 11327600 Artis icono floor- Model No....
The Issue: Siemens has become aware of a potential hardware issue with Artis Q, Artis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q floor- Model No. 10848280 Artis Q ceiling- Model Recalled by Siemens...
The Issue: Siemens has become aware of a potential hardware issue with Artis Q, Artis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis pheno- Model No. 10849000 Recalled by Siemens Medical Solutions USA,...
The Issue: Siemens has become aware of a potential hardware issue with Artis Q, Artis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The BioZorb LP Marker is an implantable radiopaque marker used Recalled by...
The Issue: Hologic BioZorb LP Marker, (Product number F0221), lot number 22A0RL,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter CLEARLINK System Recalled by Baxter Healthcare Corporation Due to...
The Issue: Firm noted an increase in customer reports of leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Subdermal Needle Electrode Recalled by Technomed Europe Due to...
The Issue: Burns of varying degrees can occur to patients with electrodes left in while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Timolol Maleate Ophthalmic Solution Recalled by Akorn, Inc Due to...
The Issue: Identification of an unknown impurity at the 12-month stability point....
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CoViPoint COVID test kit (MultiPLEX/Direct) Kit Item Numbers: BC-DK0200...
The Issue: Distribution of COVID Test Kits without FDA Approval, Clearance or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nighttime Sleep-Aid (doxylamine succinate HCl) tablets Recalled by LNK...
The Issue: Labeling: Not Elsewhere Classified: Carton incorrectly identifies product as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetaminophen Injection Recalled by Baxter Healthcare Corporation Due to...
The Issue: Temperature Abuse: Product distributed in trucks with labels attached to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eclectic Herb Vitamin Herb Blend vita biotic dietary supplement Recalled by...
The Issue: Product's ingredients names such as Oregon Grape, Cayenne Root, and Ginger...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: LineSider Spinal System pedicle screws Recalled by Integrity Implants Inc....
The Issue: Potential for intraoperative screw head separation at weld location.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker EVOLVE Recalled by Wright Medical Technology, Inc. Due to The outer...
The Issue: The outer label does not match the device inside the package. The affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker EVOLVE Recalled by Wright Medical Technology, Inc. Due to The outer...
The Issue: The outer label does not match the device inside the package. The affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE CLEARPRO TRACH T-PIECE CLOSED SUCTION CATHETER Recalled by MEDLINE...
The Issue: Potential for the suction catheter to come apart from the green connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE CLEARPRO TRACH DOUBLE SWIVEL CLOSED SUCTION CATHETER Recalled by...
The Issue: Potential for the suction catheter to come apart from the green connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE CLEARPRO DOUBLE SWIVEL CLOSED SUCTION CATHETER Recalled by MEDLINE...
The Issue: Potential for the suction catheter to come apart from the green connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zynrelef (bupivacaine and meloxicam) Recalled by HERON THERAPEUTICS, INC....
The Issue: Defective Delivery System: An incorrect 10 mL (12 mL) Luer (slip) syringe...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Difluprednate Ophthalmic Emulsion 0.05% Recalled by CIPLA Due to Lack of...
The Issue: Lack of Assurance of Sterility: Complaints received of defective container...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FABCO ORS DENTAL ROLLS Recalled by Carwild Corporation Due to Sterility with...
The Issue: Sterility with new cotton source not validated
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.