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.
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High - Class I · 1+ years ago
E.A. Sween Company Pulled Pork Sandwich products recall: Product Contamination
Product Contamination
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Elevated risk · 1+ years ago
Martin’s and Giant/Casa Mamita Taco Dinner Kits recall: May contain undeclared milk
May contain undeclared milk.
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High - Class I · 1+ years ago
Hormel Foods Corporation Ready-To-Eat Frozen Chicken products recall: Product Contamination
Product Contamination
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NHTSA safety recall · 1+ years ago
Ford recall: The windshield glass may have visible air bubbles
The windshield glass may have visible air bubbles, which can obscure the driver's visibility. As such, these vehicles fail to comply with the…
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High - Class I · 1+ years ago
LSI, Inc. BBQ Pork Jerky products recall: Product Contamination
Product Contamination
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NHTSA safety recall · 1+ years ago
Chrysler Ram ProMaster recall: The electrical circuit for the radiator fan may overheat
The electrical circuit for the radiator fan may overheat.
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NHTSA safety recall · 1+ years ago
Honda CB1000SP Hornet SP recall: The pivot bolt on the gearshift pedal may loosen and detach
The pivot bolt on the gearshift pedal may loosen and detach, resulting in the inability to shift gears. As such, these motorcycles fail to comply…
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Elevated risk · 1+ years ago
Sauna360 Tylö Halmstad and Kiruna Hybrid Saunas recall: Fall Hazard
Fall Hazard
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Highest risk · 1+ years ago
J & D Brush Bio Ionic Hair Curling Irons recall: Burn Hazard
Burn Hazard
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Class II · 1+ years ago
Baxter Healthcare Corporation Clearlink System Solution Set, Non-Vented recall: IV sets may leak
IV sets may leak.
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Class II · 1+ years ago
Microvention Inc. Flow Re-Direction Endoluminal Devices: Fred 27 recall: Flow diverter may have a manufacturing issue related to the tantalum length
Flow diverter may have a manufacturing issue related to the tantalum length and/or tantalum attachment pattern, which may lead the device to be…
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Class I · 1+ years ago
Bronchovideoscope Olympus BF-Q170 recall: Additional IFU updates to provide further clarification on safe and effective
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma…
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Class II · 1+ years ago
Baxter Healthcare Corporation Clearlink System Extension SET recall: IV sets may leak
IV sets may leak.
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Class II · 1+ years ago
American Contract Systems Inc. Medical convenience kits recall: Identified products were re-gassed (sterilized more than once) after
Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection…
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Class I · 1+ years ago
OES Bronchofiberscope Olympus BF Type MP60 recall: Additional IFU updates to provide further clarification on safe and effective
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma…
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Class II · 1+ years ago
American Contract Systems Inc. Medical convenience kits recall: Identified products were re-gassed (sterilized more than once) after
Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection…
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Class II · 1+ years ago
Boston Scientific Corporation CX Preconnect with Tenacio Pump with InhibiZone recall: The potential for devices to experience inflation and/or deflation
The potential for devices to experience inflation and/or deflation performance issues or difficulties.
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Class I · 1+ years ago
Evis Exera II Bronchovideoscope Olympus BF Type Q180 recall: Additional IFU updates to provide further clarification on safe and effective
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma…
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Class II · 1+ years ago
American Contract Systems Inc. Medical convenience kits recall: Identified products were re-gassed (sterilized more than once) after
Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection…
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Class I · 1+ years ago
Evis Exera II Bronchovideoscope Olympus BF Type 1TQ180 recall: Additional IFU updates to provide further clarification on safe and effective
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma…
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Class II · 1+ years ago
American Contract Systems Inc. Medical convenience kits recall: Identified products were re-gassed (sterilized more than once) after
Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection…
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Class II · 1+ years ago
Contego Medical LLC Neuroguard IEP 3 in 1 recall: Carotid stent and post-dilation balloon system with integrated embolic
Carotid stent and post-dilation balloon system with integrated embolic protection system has an integrated filter that may not open or may not fully…
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Class II · 1+ years ago
Philips North America Cardiac Workstation 7000 recall: Failure of Environmental Stress Testing from a pinched power module wire
Failure of Environmental Stress Testing from a pinched power module wire within the housing of the Cardiac Workstation device which resulted in a…
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Class II · 1+ years ago
Medline Adult Anesthesia Set, REF DYNJ39985G recall: Specific items and lots of Medline Kits may contain Clearlink IV Sets
Specific items and lots of Medline Kits may contain Clearlink IV Sets which Baxter recalled due to customer reports of leaking.