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. 2,411 recalls have been distributed to District of Columbia in the last 12 months.
Showing 40021–40040 of 47,654 recalls
Recalled Item: Vitamin B12 Cyanocobalamin with MIC Injection USP 1000 mcg/ml Recalled by...
The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vitamin B6 Pyridoxine HCL for Injection USP Recalled by Medical Supply...
The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lipo 8 Injection USP 200 mg/ml Recalled by Medical Supply Liquidators Llc...
The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: McKesson Cardiology Hemo. McKesson Cardiology" Hemo is intended for complete...
The Issue: McKesson Cardiology Hemo front-end parameter boxes must undergo annual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The synthetic non-absorbable surgical sutures CARDIOFLON Evolution are...
The Issue: A potential splitting of the surface treatment of the thread ends on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The synthetic non-absorbable surgical sutures CARDIOXYL are composed of a...
The Issue: A potential splitting of the surface treatment of the thread ends on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxygen Mask Recalled by Salter Labs Due to The case label correctly states...
The Issue: The case label correctly states partial rebreather but the insert label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental Tapered Screw-Vent Implant Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Dental is conducting a voluntary recall of a single lot of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Essential NEO Recalled by Karl Storz Endoscopy Due to KARL STORZ...
The Issue: KARL STORZ Endoscopy-America is recalling the Essential NEO because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Doctor's Best Red Yeast Rice 1200 Recalled by Doctor's Best, Inc. Due to...
The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis discovered undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bard Peripherally Inserted Central Catheter (PICC) and Dialysis catheter...
The Issue: Potential for inadvertent scalpel stick injury involving the safety scalpel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sonopet Ultrasonic Surgical System Console Recalled by Stryker Instruments...
The Issue: The firm received complaints regarding insufficient irrigation to the tip of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MK5 NX Controller--Wheelchair controller Recalled by Invacare Corporation...
The Issue: M41 Powered Wheelchairs received through Invacare Service Parts (ISP) have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis EMPIRA NC RX PTCA Dilatation Catheter Recalled by Cordis Corporation...
The Issue: The balloon may exhibit resistance to the removal of the balloon cover....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis EMPIRA RX PTCA Dilatation Catheter Recalled by Cordis Corporation Due...
The Issue: The balloon may exhibit resistance to the removal of the balloon cover....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS ADVIA Centaur CP Immunoassay System BNP kit Recalled by Siemens...
The Issue: Complaints of failed calibration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS ADVIA Centaur CP Immunoassay System BNP kit Recalled by Siemens...
The Issue: Complaints of failed calibration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT: product code 882482 Recalled by Philips Medical Systems...
The Issue: Flat Panel Display (FPD) failed to remain securely locked in the deployed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Famotidine for Oral Suspension Recalled by Novel Laboratories, Inc. Due to...
The Issue: Failed Impurity/Degradation Specification; 12-month stability time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tolterodine Tartrate Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications; Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.