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. 2,616 recalls have been distributed to District of Columbia in the last 12 months.
Showing 8101–8120 of 27,451 recalls
Recalled Item: Non-Sterile Double Ended Trial Kit Recalled by restor3d Inc. Due to Product...
The Issue: Product labeled incorrectly. The lot was labeled with Small footprint when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evans Wedge Disposable Trials Recalled by restor3d Inc. Due to During...
The Issue: During re-work of disposable instruments to relabel for 4-year shelf-life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedMinder Medication Dispenser- Intended to serve as a medication reminder...
The Issue: Discontinuation of the Emergency Alert watch or pendant will no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smart Toe II Intramedullary Arthrodesis Implant Recalled by Stryker GmbH Due...
The Issue: The nickel-sensitivity statement on the outer carton may be partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Anti-Kappa PE (Cat. No. 346587) is an analyte specific Recalled by...
The Issue: Anti-Kappa APC & Anti-Kappa PE analyte reagents may exhibit uncharacteristic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Anti-Kappa APC (Cat. No. 341098) is an analyte specific Recalled by...
The Issue: Anti-Kappa APC & Anti-Kappa PE analyte reagents may exhibit uncharacteristic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products LH Reagent Pack Product Code: 1350198...
The Issue: Falsely high or delayed patient and QC results may occur due to low end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Prolactin Reagent Pack Product Code:...
The Issue: Falsely high or delayed patient and QC results may occur due to low end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products FSH Reagent Pack- IVD 1931922 Recalled by...
The Issue: Falsely high or delayed patient and QC results may occur due to low end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Uretero-reno videoscope Recalled by Olympus Corporation of the...
The Issue: The bending section of the URF-V2 may crack, resulting in an abnormal shape...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire Recalled by Arthrex, Inc. Due to Products do not meet length and...
The Issue: Products do not meet length and diameter specifications.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Medtronic formerly...
The Issue: The audible alarm may not sound and/or the omni-directional LED visual alarm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inactivated macrolide and quinolone-resistant Mycoplasma genitalium Recalled...
The Issue: QC process was not adequate for the specification range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott SE TactiCath Sensor Enabled Contact Force Ablation Catheter Recalled...
The Issue: Devices were manufactured with a "First Use Date" preprogrammed in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott SE TactiCath Sensor Enabled Contact Force Ablation Catheter Recalled...
The Issue: Devices were manufactured with a "First Use Date" preprogrammed in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic IN.PACT AV Recalled by Medtronic Vascular, Inc. Due to Packaging...
The Issue: Packaging for Balloon Catheters may be damaged resulting in loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic IN.PACT Admiral Recalled by Medtronic Vascular, Inc. Due to...
The Issue: Packaging for Balloon Catheters may be damaged resulting in loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TearCare version 1.0 SmartHubs Recalled by Sight Sciences, Inc. Due to...
The Issue: Ophthalmic devices distributed prior to the recently-obtained 510(k)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra Pure Non-Woven Sponges Non-Sterile 4-Ply 5 Recalled by Steris...
The Issue: Product not approved for release for US distribution
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra Pure Non-Woven Sponges Non-Sterile 4-Ply 2 Recalled by Steris...
The Issue: Product not approved for release for US distribution
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.