Recalls affecting District of Columbia
Notices that name District of Columbia in their distribution area, plus every nationwide recall — nationwide recalls reach District of Columbia too.
-
Class II · 9 months ago
Philips Medical Systems Nederland B.v. Allura Xper FD10 recall: Philips has identified that in a limited number of impacted systems the drip
Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field…
-
Class II · 9 months ago
Medline Kits containing B. Braun IV Administration Sets and Pump recall: Medline kits contain B. Braun IV Administration Sets and Pump Administration
Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the…
-
Class II · 9 months ago
Medline Kits containing B. Braun IV Administration Sets and Pump recall: Medline kits contain B. Braun IV Administration Sets and Pump Administration
Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the…
-
Class II · 9 months ago
C-Rad Positioning Ab Brand Name: Catalyst+ Product Name: Catalyst, Catalyst+ Model/ recall: Due to issues with the system's stereotactic radiosurgery (SRS) treatment
Due to issues with the system's stereotactic radiosurgery (SRS) treatment cannot be guaranteed for all couch angles and system setups. n certain…
-
Class II · 9 months ago
Philips Medical Systems Nederland B.v. Allura Xper FD20 Biplane recall: Philips has identified that in a limited number of impacted systems the drip
Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field…
-
Class II · 9 months ago
Philips Medical Systems Nederland B.v. Allura Xper FD20 OR Table recall: Philips has identified that in a limited number of impacted systems the drip
Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field…
-
Class II · 9 months ago
Medline Kits containing B. Braun IV Administration Sets and Pump recall: Medline kits contain B. Braun IV Administration Sets and Pump Administration
Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the…
-
Class II · 9 months ago
Medline Kits containing B. Braun IV Administration Sets and Pump recall: Medline kits contain B. Braun IV Administration Sets and Pump Administration
Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the…
-
Class II · 9 months ago
Medline medical procedure convenience kits labeled as: 1) WCH recall: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators
Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the…
-
Class II · 9 months ago
Medline medical procedure convenience kits labeled as: 1) Thoracic recall: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators
Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the…
-
Class II · 9 months ago
Boston Scientific Coyote Over-The-Wire PTA Balloon Dilation Catheter recall: Boston Scientific is initiating the removal of certain batches of Coyote"
Boston Scientific is initiating the removal of certain batches of Coyote" Over-the-Wire (OTW) Percutaneous Transluminal Angioplasty (PTA) Balloon…
-
Class II · 9 months ago
Medtronic Inc Abre Venous Self-Expanding Stent System, Model numbers AB9G14120090 recall: Stents may be impacted by a Nitinol anomaly which causes a reduced stent
Stents may be impacted by a Nitinol anomaly which causes a reduced stent diameter when deployed and corresponding reduced radial force. Issue may…
-
Class II · 9 months ago
ICU Medical, Inc. Plum Duo Infusion System, List Number 40002-04-01 recall: ICU Medical received one lot of defective primary speakers from our supplier
ICU Medical received one lot of defective primary speakers from our supplier that may fail to produce an audible sound. If the primary speaker in…
-
Class II · 9 months ago
Thoratec LLC CentriMag Blood Pump, REF: 102953, 201-20003, 201-90010, 201-90016 recall: Acute circulatory support system pump may not fit into the motor and reports
Acute circulatory support system pump may not fit into the motor and reports received of the pump not being securely locked into the motor using the…
-
Class II · 9 months ago
Instrumentation Laboratory The product is used for the evaluation of the intrinsic recall: Potential for microbial contamination
Potential for microbial contamination.
-
Class II · 9 months ago
Philips Medical Systems Nederland B.v. Allura Xper FD20 Biplane recall: Philips has identified that in a limited number of impacted systems the drip
Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field…
-
Class II · 9 months ago
Medline Kits containing B. Braun IV Administration Sets and Pump recall: Medline kits contain B. Braun IV Administration Sets and Pump Administration
Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the…
-
Class II · 9 months ago
Medline Kits containing B. Braun IV Administration Sets and Pump recall: Medline kits contain B. Braun IV Administration Sets and Pump Administration
Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the…
-
Class II · 9 months ago
Medicrea, IB3D Universal Implant Inserter recall: Due to complaints, orthopedic rotation tool handle may untread from the shaft
Due to complaints, orthopedic rotation tool handle may untread from the shaft resulting in the inability to rotate implant.
-
Class II · 9 months ago
ICU Medical Inc. Portex Spinal Tray recall: Affected lots of syringes may have a crack on the syringe collar
Affected lots of syringes may have a crack on the syringe collar, which may lead to delayed or repeated blood draw/fluid delivery. This issue may…
-
Class II · 9 months ago
Philips Medical Systems Nederland B.v. Allura Xper FD10 recall: Philips has identified that in a limited number of impacted systems the drip
Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field…
-
Class II · 9 months ago
Mobius Imaging, LLC Detachable 10in Pendant Upgrade component for the AIRO Computed recall: AIRO pendant replacement kits and upgrade do not possess the "Safe Hand
AIRO pendant replacement kits and upgrade do not possess the "Safe Hand Position Warning" label.
-
Class II · 9 months ago
Fresenius Kabi USA, LLC Ivenix Infusion System , LVP Software: LVP-SW-0005 recall: Emphasizing instructions for LVP duration programming located in the IFU
Emphasizing instructions for LVP duration programming located in the IFU.
-
Class II · 9 months ago
Philips Azurion Systems with software versions R2.1.10 and R2.2.10 recall: Six (6) identified software issues which may result in the following: system
Six (6) identified software issues which may result in the following: system keeps restarting, AMC triple drive, C-Partition of Suite PC running out…