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. 2,612 recalls have been distributed to District of Columbia in the last 12 months.
Showing 9401–9420 of 27,451 recalls
Recalled Item: FRESH DAY 1 DAY TORIC Power -07.50 -0.75/060 Daily Disposable Recalled by...
The Issue: Misaligned placement of an axis mark can cause the patient to experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARITI 1 DAY TORIC Power: -07.50 -0.75/060 Daily Disposable Contact...
The Issue: Misaligned placement of an axis mark can cause the patient to experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Pacing Catheter Kit-Bipolar Electrode Catheter 5 Fr. 110 cm Recalled...
The Issue: Marketed without a 510K
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Temporary Pacing Catheter/Introducer Kit 6Fr. pacing catheter 7Fr....
The Issue: Marketed without a 510K
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Bipolar Balloon Electrode Catheter 5 Fr. 105 cm Recalled by Arrow...
The Issue: Marketed without a 510K
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Temporary Pacing Catheter/Introducer Kit 5Fr. pacing catheter 6 Fr....
The Issue: Marketed without a 510K
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5 Fr IR PowerPICC Convenience Kit Catheter Dual Lumen with Recalled by Bard...
The Issue: Catheter convenience kits contain the incorrect guidewire. Kits were labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GENOSYL DS Recalled by Vero Biotech, LLC Due to Reports received of NO...
The Issue: Reports received of NO measured below desired dose during transition between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION Posterior Stabilized OXINIUM Femoral Component Recalled by Smith &...
The Issue: The device components experienced a manufacturing process error that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cortoss Bone Augmentation Material 5cc Cartridge Recalled by Stryker Spine...
The Issue: The products experienced a 12-hour excursion from the required temperature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cortoss Bone Augmentation Material 10cc Cartridge Recalled by Stryker Spine...
The Issue: The products experienced a 12-hour excursion from the required temperature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ADVIA Chemistry XPT Chemistry System Recalled by Siemens Healthcare...
The Issue: ADVIA Chemistry System and Software Versions (V1.4 SMN 11314625 and V1.4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JELCO HYPODERMIC NEEDLE-PRO FIXED NEEDLE INSULIN SYRINGE: a) 1.0mL 28G...
The Issue: Specific models and lot numbers of the Jelco Hypodermic Needle-Pro Fixed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic LINQ II Model Number # LNQ22 Insertable Cardiac Monitor Recalled...
The Issue: Device fail to detect Brady episodes, Pause (Asystole) episodes and PVC's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PORTEX UNLTRperc Percutaneous Dilation Tracheostomy Kit Recalled by Smiths...
The Issue: One lot number of a specific model of ULTRAperc Percutaneous Dilation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Angio Cath Removal Tray Recalled by DeRoyal Industries Inc Due to...
The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExacTrac Dynamic software Recalled by Brainlab AG Due to Display of...
The Issue: Display of potential patient movement might be delayed to the user for high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Heart Cath Procedure Pack Recalled by DeRoyal Industries Inc Due to...
The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Pacemaker Tray Pgybk Recalled by DeRoyal Industries Inc Due to...
The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer - multi-component system for in vitro Recalled by...
The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.