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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Class II · 7 months ago
Teva Pharmaceuticals USA, Inc Octreotide Acetate for Injectable Suspension recall: Lack of Assurance of Sterility: Quality system deficiencies identified during
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the…
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Class II · 7 months ago
Teva Pharmaceuticals USA, Inc Octreotide Acetate for Injectable Suspension recall: Lack of Assurance of Sterility: Quality system deficiencies identified during
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the…
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Class II · 7 months ago
Macleods Pharma USA, Inc Levothyroxine Sodium Tablets USP 150 mcg, 1000 Tablets bottle recall: Subpotent Drug
Subpotent Drug
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Class II · 7 months ago
Teva Pharmaceuticals USA, Inc Octreotide Acetate for Injectable Suspension recall: Lack of Assurance of Sterility: Quality system deficiencies identified during
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the…
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Class I · 7 months ago
Nuts.com Inc. Nuts.com, Espresso Malted Milk Balls, 1 lb. sealed pouch & 20 lb. clear recall: Undeclared Allergen - Wheat and Soy (from Soy Lecithin). The ingredient
Undeclared Allergen - Wheat and Soy (from Soy Lecithin). The ingredient statement and allergen information do not include wheat or soy.
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Class II · 7 months ago
Western Mixers Produce & Nuts, Inc. Chilli Spanish Peanuts, First Street brand recall: Foreign object (glass) found inside sealed container of finished product
Foreign object (glass) found inside sealed container of finished product.
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Class II · 7 months ago
Western Mixers Produce & Nuts, Inc. Chilli Spanish Peanuts, Treasured Harvest brand recall: Foreign object (glass) found inside sealed container of finished product
Foreign object (glass) found inside sealed container of finished product.
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Elevated risk · 7 months ago
Kian Pee Wan Dietary supplement capsules marketed for treatment for gaining weight recall: Device & Drug Safety/Unapproved Drug
Device & Drug Safety/Unapproved Drug
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Elevated risk · 7 months ago
Vital Nutrient Aller-C Dietary Supplement recall: Undeclared egg, hazelnut and soy
Undeclared egg, hazelnut and soy
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NHTSA safety recall · 7 months ago
Mercedes-Benz G580 recall: The incorrect wheel bolts may have been installed during vehicle manufacturing
The incorrect wheel bolts may have been installed during vehicle manufacturing.
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NHTSA safety recall · 7 months ago
Honda CB1000SP recall: The fuel feed hose may disconnect from the fuel tank, causing a fuel leak
The fuel feed hose may disconnect from the fuel tank, causing a fuel leak.
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NHTSA safety recall · 7 months ago
Chrysler Pacifica and Voyager recall: The right and left side curtain air bags may have insufficient pressure
The right and left side curtain air bags may have insufficient pressure retention. As such, these vehicles fail to comply with the requirements of…
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Highest risk · 7 months ago
Vive Health Adult Portable Bed Rails recall: Risk of Serious Injury or Death from Entrapment and Asphyxiation
Risk of Serious Injury or Death from Entrapment and Asphyxiation; Two Deaths Reported
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Highest risk · 7 months ago
Petzl America Nomic and Ergonomic Ice Climbing Axes recall: Fall Hazard; Risk of Serious Injury or Death
Fall Hazard; Risk of Serious Injury or Death
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NHTSA safety recall · 7 months ago
Volvo Trucks VNL recall: The service brake may take longer than expected to release
The service brake may take longer than expected to release. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle…
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NHTSA safety recall · 7 months ago
Volvo Trucks VNL recall: The instrument panel may fail while driving
The instrument panel may fail while driving. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard…
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NHTSA safety recall · 7 months ago
Volkswagen Jetta and Taos recall: The instrument panel may fail to display warning lights or gauges
The instrument panel may fail to display warning lights or gauges. As such, these vehicles fail to comply with the requirements of Federal Motor…
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Class II · 7 months ago
Convatec, EsteemBody Drainable Pouch REF:423657 10-35mm recall: Drainable large pouch may leak due to manufacturing issue
Drainable large pouch may leak due to manufacturing issue.
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Class II · 7 months ago
GE Medical Systems, LLC Centricity Universal Viewer Software Versions 7.0 through 7.0 recall: There is a potential cybersecurity vulnerability affecting certain versions
There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on…
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Class II · 7 months ago
Baxter Healthcare Corporation Brand Name: Welch Allyn recall: Display screen may unintentionally flicker due to a software issue. Exposure
Display screen may unintentionally flicker due to a software issue. Exposure to flickering lights may induce photosensitive seizure activity in…
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Class II · 7 months ago
Abbott Diagnostics Scarborough, Inc. Product Name: ID NOW" Influenza A & B 2 Model/ recall: It was confirmed that the impacted lot has a higher occurrence of invalid
It was confirmed that the impacted lot has a higher occurrence of invalid rates when compared to the product Instructions for Use.
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Class II · 7 months ago
GE Medical Systems, LLC Centricity Universal Viewer Software Versions 5.0 SP6 through recall: There is a potential cybersecurity vulnerability affecting certain versions
There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on…
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Class II · 7 months ago
Hologic, Inc. Brand Name: Aptima HPV Assay Product Name: Aptima HPV Assay Model/ recall: Due to product exhibiting potential to generate either invalid or false
Due to product exhibiting potential to generate either invalid or false negative results.
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Class II · 7 months ago
Stryker Medical Division of Stryker Corporation Cub Pediatric Crib, Model FL19H recall: Cribs sold in the USA are missing two access door warning labels
Cribs sold in the USA are missing two access door warning labels.