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. 891 recalls have been distributed to District of Columbia in the last 12 months.
Showing 45821–45840 of 47,654 recalls
Recalled Item: The TM Ardis Interbody System Inserter Stainless Steel Recalled by Zimmer,...
The Issue: Zimmer Spine is has received complaints of difficulty in turning the implant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX PENTRA ML Recalled by Horiba Instruments, Inc dba Horiba Medical Due to...
The Issue: Horiba Medical is recalling ABX PENTRA ML because they have confirmed an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware that patient mismatch without a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S5 Double Roller Pump 85 Recalled by Sorin Group USA, Inc. Due to Sorin...
The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sorin C5 Perfusion System Recalled by Sorin Group USA, Inc. Due to Sorin...
The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helion and Xenion surgical lights Recalled by Trumpf Medical Systems, Inc....
The Issue: Incidents regarding fractures of the front joint of the spring arm have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Male Recalled by Cure Medical LLC Due to The firm initiated the product...
The Issue: The firm initiated the product recall because labeling on some of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S5 Single Roller Pump 150 Recalled by Sorin Group USA, Inc. Due to Sorin...
The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S5 Mast Roller Pump 85 Recalled by Sorin Group USA, Inc. Due to Sorin Group...
The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S5 Mast Roller Pump 150 Recalled by Sorin Group USA, Inc. Due to Sorin Group...
The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareStream Dental CS 2100 X-ray system Product Usage: The expected Recalled...
The Issue: There have been approximately 2% of the x-ray generators manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iris Diagnostics Division iQ Control/Focus Set Recalled by Iris Diagnostics...
The Issue: The firm initiated this recall because complaints from customers reported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mx8000 IDT Whole Body Computed Tomography X-ray system Distributed by...
The Issue: The low contrast pins in the Image Quality (IQ) phantom deteriorates over...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrig Trigger Release Sterile Micro Hook Blade Product Usage: The...
The Issue: Instratek, Inc.has received multiple complaints of the 1052 Trigger Finger...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ MOSAIQ is an image-enabled electronic medical record system (EMR)...
The Issue: A patient was seriously mistreated after a user made and saved an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareStream Dental Kodak 2200 Intraoral X-ray system Product Usage: The...
The Issue: There have been approximately 2% of the x-ray generators manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareStream Dental CS 2200 X-ray system Product Usage: The expected Recalled...
The Issue: There have been approximately 2% of the x-ray generators manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareStream Dental Kodak 2100 Intraoral X-ray system Product Usage: The...
The Issue: There have been approximately 2% of the x-ray generators manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Popcorn Indiana Bacon Ranch Popcorn Net Wt. 3.5 oz - Recalled by Dale &...
The Issue: Various flavors of popcorn were manufactured on a conveyor belt which tested...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Popcorn Indiana Dark Fudge Chocolate Chip Kettlecorn Net Wt. 5.5 oz Recalled...
The Issue: Various flavors of popcorn were manufactured on a conveyor belt which tested...
Recommended Action: Do not consume. Return to store for a refund or discard.