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. 2,395 recalls have been distributed to District of Columbia in the last 12 months.
Showing 43001–43020 of 47,654 recalls
Recalled Item: DICOM Export Format for Sum Dose with Velocity v3.0.0. A Recalled by...
The Issue: An anomaly was detected such that, under certain conditions, a summed dose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic O-arm Imaging System Mobile X-ray system. Model No. BI-700-00027...
The Issue: Review of on-system electronic product labeling and Instructions for comply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD 100NX Cassettes Recalled by Advanced Sterilization Products Due to...
The Issue: The recall of the STERRAD 100NX Cassettes was initiated because Advanced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KIT cobas 4800 HPV AMP/DET 240T / 960T US-IVD Recalled by Roche Molecular...
The Issue: During an internal investigation, a formulation error that occurred was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DIANEAL Low Calcium (2.5 mEq/L) Peritoneal Dialysis Solution with 1.5%...
The Issue: Defective Container: There is a potential for frangible components to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GYRUS ACMI Recalled by Gyrus Medical, Inc Due to On April 29, 2013 Olympus...
The Issue: On April 29, 2013 Olympus Surgical Technologies America R&D received results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.2mm Drill Bit. This is a component within the PediLoc Recalled by...
The Issue: OrthoPediatrics has initiated a voluntary recall of Part # 01-1050-002,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nestle Nutrition Recalled by Nestle HealthCare Nutrition Due to Nestle...
The Issue: Nestle HealthCare Nutrition, Inc. is initiating a recall on some of Compat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terazosin Hydrochloride Capsules Recalled by Teva Pharmaceuticals USA, Inc....
The Issue: Labeling -label error on declared strength: unopened, sealed bottle of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Stereotactic Circular Collimator - 3D Line stereotatic Hardware Accessories...
The Issue: Potential for clinical errors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRI Cocaine Metabolite Assay Recalled by Microgenics Corp Due to...
The Issue: Surveillance of reagent stability for specific lots of DRI Cocaine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Super-DMZ Rx 2.0 Capsules Recalled by Mira Health Products Ltd. Due to...
The Issue: Marketed without an Approved NDA/ANDA; product contains the steroid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: B-50 capsules Recalled by Mira Health Products Ltd. Due to Marketed without...
The Issue: Marketed without an Approved NDA/ANDA; product found to contain methasterone...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: METHA-DROL Extreme capsules Recalled by Mira Health Products Ltd. Due to...
The Issue: Marketed without an Approved NDA/ANDA; product found to contain dimethazine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olanzapine Tablets Recalled by Torrent Pharma Inc Due to Defective...
The Issue: Defective Container; This action is being taken as a precautionary measure...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tapered Navigator Certain Surgical Kit Product Usage: Molded plastic tray...
The Issue: During recent revised sterilization validation testing, the included...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navigator Surgical Kit Product Usage: Molded plastic tray used in Recalled...
The Issue: During recent revised sterilization validation testing, the included...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contra-Angle Torque Driver Kit Product Usage: Molded plastic tray used...
The Issue: During recent revised sterilization validation testing, the included...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contra-Angle Torque Driver Kit For Certain Internal Connection Product...
The Issue: During recent revised sterilization validation testing, the included...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contra-Angle Torque Driver Kit For Certain and External Connection Product...
The Issue: During recent revised sterilization validation testing, the included...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.