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. 2,360 recalls have been distributed to District of Columbia in the last 12 months.
Showing 46541–46560 of 47,654 recalls
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: 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: Advanta 2 Bed. The Advanta 2 Bed is intended for Recalled by Hill-Rom, Inc....
The Issue: During an evaluation of Advanta 2 siderail samples returned from the field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: superDimension Systems AAS00016-xx with Software Version 4.0-4.9. Indicated...
The Issue: superDimension, Inc., is conducting a recall of certain superDimension...
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: 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: 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: 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: ZEE Antiseptic Wipes Recalled by Dukal Corp. Due to Microbial contamination...
The Issue: Microbial contamination of Non Sterile Product; contamination with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dukal Corporation BZK Swab Recalled by Dukal Corp. Due to Microbial...
The Issue: Microbial contamination of Non Sterile Product; contamination with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kleenex Luxury Foam Hand Sanitizer Recalled by Kimberly-Clark Corporation...
The Issue: Microbial Contamination of Non-Sterile Products; The affected lots were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kleenex Foam Hand Sanitizer Recalled by Kimberly-Clark Corporation Due to...
The Issue: Microbial Contamination of Non-Sterile Products; The affected lots were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IQF Oysters 3lbs Recalled by KOREAN FARM, INC. Due to Korean Farm is...
The Issue: Korean Farm is recalling Assi Brand Korean Oysters because they have been...
Recommended Action: Do not consume. Return to store for a refund or discard.
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: 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: Ocean Manna Korean IQF Oysters Recalled by Pacific Giant, Inc Due to Pacific...
The Issue: Pacific Giant is recalling all frozen (IQF) oyster meat and 1/2 shell...
Recommended Action: Do not consume. Return to store for a refund or discard.
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.
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: 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.