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. 2,459 recalls have been distributed to District of Columbia in the last 12 months.
Showing 23941–23960 of 27,451 recalls
Recalled Item: Optiflux F18Nre Flux Dialyzers Recalled by Fresenius Medical Care Holdings,...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F180NRe High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F200NRe High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux B200 Flux Dialyzers Recalled by Fresenius Medical Care Holdings,...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F160NR High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F160NRe High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator used Model numbers: M3535A...
The Issue: HeartStart MRx Defibrillator Monitor therapy connection could experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nice-En-Smooth Berry Burst Recalled by Altasource LLC dba Meta Labs LLC Due...
The Issue: Firm is not registered as a drug manufacturer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mega-Gen His Personal Lubricant Recalled by Altasource LLC dba Meta Labs LLC...
The Issue: Firm is not registered as a drug manufacturer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amo-O Herbal Stimulator Recalled by Altasource LLC dba Meta Labs LLC Due to...
The Issue: Firm is not registered as a drug manufacturer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hot Ice Recalled by Altasource LLC dba Meta Labs LLC Due to Firm is not...
The Issue: Firm is not registered as a drug manufacturer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Citation TMZF HA 132 degrees Neck Angle Recalled by Stryker Howmedica...
The Issue: Stryker received a report from the field indicating that a citation TMZF HA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Recalled by Siemens Medical Solutions Diagnostics Due to There...
The Issue: There is a potential for incorrect results to be reported from processing of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OneTray Sealed Sterilization Containers Product Usage: A rigid sterilization...
The Issue: The wrong sterilization time was on the label. The label lists Steam Gravity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otto Bock Aerial and Aerial Active Wheelchair Cushions. Material numbers:...
The Issue: Otto Bock is recalling all Aerial and Aerial Active Wheelchair Cushions from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar infusion pump Recalled by Hospira Inc. Due to The connection between...
The Issue: The connection between the beeper subassembly and the pump may fail. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAQUET PLEGIOX Cardioplegia Heat Exchanger The PLEGIOX Cardioplegia Heat...
The Issue: The MAQUET post-marketing vigilance program has identified a discrepancy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE1055: Prevena Dressing Recalled by KCI USA, INC. Due to Prevena...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE2001: Prevena Incision Management Customizable System Box Product Usage:...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes CMF Battery Powered Driver Recalled by Synthes, Inc. Due to The CMF...
The Issue: The CMF Battery Powered Driver graphic case contains outlines of the Battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.