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. 2,448 recalls have been distributed to District of Columbia in the last 12 months.
Showing 26741–26760 of 27,451 recalls
Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSI Stealth 360-degree Orbital Atherectomy Device (OAD) Recalled by...
The Issue: CSI has initiated a recall on specific lot numbers of Stealth 360-degree...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Modular Perfusion System 9000 Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varian brand Varian Eclipse Treatment Planning System for radiotherapy...
The Issue: Varian has identified an anomaly with the Eclipse Treatment Planning (for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Modular Perfusion System 9000 Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Modular Perfusion System 8000 base Recalled by Terumo Cardiovascular...
The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1. System 1 base 100/120V. The Recalled by...
The Issue: Terumo Cardiovascular Systems has received several reports of malfunctions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIRS for MATRIX Spine System. Minimally Invasive Reduction Screw (MIRS)...
The Issue: Synthes is initiating a Medical Device Labeling Correction following a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom surgical kits and trays: GEO-MED TOTAL KNEE PACK PGYBK Recalled by...
The Issue: Surgical kits and trays contain Stryker Hytrel Togas which were recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Echelon MRI System/Oasis MRI Recalled by Hitachi Medical Systems...
The Issue: Hitachi discovered a software error with a feature called Multi-Planar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioDynamics Angiographic catheter --- Soft-Vu (JB-1) Non-braided. ---...
The Issue: AngioDynamics is recalling one lot of Soft-Vu Angiographic catheters because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Module Model 8100 (formerly Medley Pump Module) Subsequent...
The Issue: The recall was initiated because Carefusion has identified a potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA Satellite Automated Multi-Parameter Analyzer This system is a fully...
The Issue: Following a single customer complaint that incorrect INR values were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Xcelera Connect Recalled by Philips Healthcare Inc. Due to Xcelera...
The Issue: Xcelera Connect R2.1 L 1 SP2 , incomplete information arriving from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The 2.7mm Drilling Guide is a reusable instrument used in Recalled by...
The Issue: Integra' s quality system noted an adverse trend in complaints for breakage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: seprafilm¿ Procedure Pack ADHESION BARRIER Re-order Number: 5086-02 Product...
The Issue: Sterility of product may be compromised due to packaging defect
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: seprafilm¿ Single Site ADHESION BARRIER Re-order Number: 6641-01 Product...
The Issue: Sterility of product may be compromised due to packaging defect
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...
The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...
The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.