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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NHTSA safety recall · 11 months ago
General Equinox EV recall: The pedestrian alert sound system may not produce a sufficient change
The pedestrian alert sound system may not produce a sufficient change in volume between the vehicle being stopped and moving at low speeds. As such…
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Highest risk · 11 months ago
Plantimex Mamisan Lidocaine Ointment Containers recall: Risk of Serious Injury or Death from Child Poisoning
Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging
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Highest risk · 11 months ago
Pedego Electric Bikes Fat Tire Trikes recall: Fall and Laceration Hazards
Fall and Laceration Hazards
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Elevated risk · 11 months ago
Currey & Company Electra Chandeliers recall: Impact Injury Hazard
Impact Injury Hazard
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Highest risk · 11 months ago
Blue Wave Above-Ground Pools 48 Inches and Taller recall: Drowning Hazard
Drowning Hazard
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NHTSA safety recall · 11 months ago
Toyota Highlander and Highlander Hybrid recall: The third row center seat belt roof anchor may have been installed
The third row center seat belt roof anchor may have been installed at an incorrect angle, preventing the seat belt from properly restraining the…
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NHTSA safety recall · 11 months ago
Kia Sportage Plug-In Hybrid Electric and Sportage recall: 2" screen and a Genuine Kia tow hitch harness accessory. Due to a software
2" screen and a Genuine Kia tow hitch harness accessory. Due to a software error, the instrument panel screen may fail. As such, these vehicles fail…
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NHTSA safety recall · 11 months ago
Vantage Mobility recall: The retractors may not lock, preventing the wheelchair from being properly
The retractors may not lock, preventing the wheelchair from being properly secured.
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NHTSA safety recall · 11 months ago
Rollx Vans recall: Please refer to Rollx's recall report for specific model year information
Please refer to Rollx's recall report for specific model year information. The retractors may not lock, preventing the wheelchair from being properly…
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Class II · 11 months ago
C.R. Bard Inc BD InLay Optima Ureteral Stent Kit Size: 8 Fr. x 26 cm recall: Labeling discrepancy; Ureteral stent actual size may not match the actual
Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
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Class III · 11 months ago
Orthofix U.S. LLC Brand Name: Forza" PTC Spacer System Product Name: Forza" PTC Spacer recall: Labeling contains claims that are not consistently present
Labeling contains claims that are not consistently present.
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Class III · 11 months ago
Orthofix U.S. LLC Brand Name: Pillar" SA PTC Spacer System Product Name: Pillar" SA recall: Labeling contains claims that are not consistently present
Labeling contains claims that are not consistently present.
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Class III · 11 months ago
Orthofix U.S. LLC Brand Name: Firebird" SI Fusion System Product Name: Firebird" SI recall: Labeling contains claims that are not consistently present
Labeling contains claims that are not consistently present.
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Class II · 11 months ago
Nipro Medical Corporation Hemodialysis System, Surdial DX REF: MC+SDX01 recall: Screw may loosen or fallout of Hemodialysis system
Screw may loosen or fallout of Hemodialysis system
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Class II · 11 months ago
Medline Perfusion Syringe, REF: Dynj39223C recall: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing BD Luer Tip Caps. BD has issued a recall of…
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Class II · 11 months ago
Medline Industries, LP Dexlock Achilles Repair Implant Kits, Makt4520 recall: There have been multiple complaints of drill bit fusing to the bushing/sleeve
There have been multiple complaints of drill bit fusing to the bushing/sleeve within the drill guide during use. Retrieving a replacement drill bit…
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Class II · 11 months ago
Stryker MV3 bariatric bed recall: Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX
Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close…
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Class II · 11 months ago
Stryker Arise 1000EX mattress recall: Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX
Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close…
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Class II · 11 months ago
Bard Peripheral Vascular Inc Safe-T-Centesis 6 Fr Catheter Drainage Tray recall: Acute drainage catheters, indicated for use in removing fluid during acute
Acute drainage catheters, indicated for use in removing fluid during acute drainage/aspiration procedure, manufactured with safety indicators that…
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Class III · 11 months ago
Orthofix U.S. LLC Brand Name: Construx" Mini PTC Spacer System Product Name: Construx" recall: Labeling contains claims that are not consistently present
Labeling contains claims that are not consistently present.
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Class III · 11 months ago
Orthofix U.S. LLC Brand Name: Construx" Mini Ti Spacer System Product Name: Construx" recall: Labeling contains claims that are not consistently present
Labeling contains claims that are not consistently present.
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Class II · 11 months ago
C.R. Bard Inc BD InLay Optima Ureteral Stent Kit Size: 4.7 Fr. x 26 cm recall: Labeling discrepancy; Ureteral stent actual size may not match the actual
Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
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Class II · 11 months ago
Datascope Corp. Cardiosave Hybrid. Intra-Aortic Balloon Pump system recall: The IFU addendum revises the Preventative Maintenance schedule to align
The IFU addendum revises the Preventative Maintenance schedule to align with the update introduced in the Service Manual as of June 2023.
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Class II · 11 months ago
Cardinal Health 200, LLC ChemoPlus gowns: Product Code recall: Affected gowns have the incorrect expiration date on the product packaging
Affected gowns have the incorrect expiration date on the product packaging. Product has a shelf-life of three years which is mislabeled on the…