Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.
The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.
Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.
Minimum severity
Maya Distribution, LLC is recalling Dragon Bali Kratom Powder and Capsules because samples collected by public health officials found the presence of Salmonella.
Kroger Specialty Pharmacy is recalling Albuterol 0.083% Inhalation Solution due to a lack of processing controls. The affected lots were dispensed in five states between December 2017 and February 2018.
Datascope is recalling the Better Bladder device because seal separation may allow air to enter the housing, potentially collapsing the balloon and reducing ECMO blood flow.
Vyaire Medical is recalling 180 AirLife Infant Resuscitation devices because the mask may stick to the elbow, making it difficult to disconnect.
Draeger Medical is recalling 26 Fabius Tiro anesthesia machines because automatic ventilation may fail if motor position detection is disturbed.
Datascope is recalling 22 units of BEQ-TOP 33700 ECC 3/8" PACK custom tubing kits because a seal defect may cause balloon collapse and reduced blood flow.
Labrada Nutrition is recalling specific lots of Lean Pro 8 Vanilla protein powder due to undeclared egg, a major food allergen.
Triangle Pharmanaturals LLC is recalling Naturally Kratom White Maeng Da capsules due to potential Salmonella contamination.
Vyaire Medical is recalling AirLife Resuscitation devices because the mask may stick to the elbow, making it difficult to disconnect.
Kroger Specialty Pharmacy is recalling Tasigna Capsules 150 mg due to a lack of processing controls. The affected units were dispensed in five states between December 2017 and February 2018.
Triangle Pharmanaturals LLC is recalling Live Well Kratom Red Maeng Da capsules in 150 and 300-count bottles due to potential Salmonella contamination.
Datascope is recalling the Better Bladder device in some custom tubing kits because seal separation may cause the balloon to collapse, potentially reducing blood flow in ECMO circuits.
Datascope is recalling the Better Bladder device in custom tubing kits because seal separation may cause balloon collapse and reduced blood flow.
Datascope is recalling 10 custom tubing kits because a seal defect may allow air to enter the housing, causing the balloon to collapse and reducing blood flow in ECMO circuits.
Triangle Pharmanaturals LLC is recalling Raw Form Organics Maeng Da Kratom Ivory White capsules because they may be contaminated with Salmonella.
Vyaire Medical is recalling 3,600 AirLife Infant Resuscitators because the mask may stick to the elbow, making it difficult to disconnect.
Draeger Medical is recalling one Fabius Tiro M anesthesia machine because automatic ventilation may fail if motor position detection is disturbed.
Triangle Pharmanaturals LLC is recalling Lifted Kratom Red Maeng Da products due to potential Salmonella contamination. The recall covers powder and capsule bottles distributed across multiple states.
Triangle Pharmanaturals LLC is recalling Lifted Kratom Gold Bali products because they may be contaminated with Salmonella.
Grato Holdings is recalling Energique herbal supplements because they are marketed as unapproved new drugs based on disease claims.
Triangle Pharmanaturals LLC is recalling Third Eye Kratom White capsules because all Kratom products from the company may be contaminated with Salmonella.
Greenbelt Greenhouse Ltd is recalling Fresh Microgreen Mix due to potential Listeria monocytogenes contamination. The product was distributed in Oregon and Washington.
Datascope is recalling 18 custom tubing kits because a seal defect may cause the Better Bladder balloon to collapse, potentially reducing blood flow in ECMO circuits.
Vitalab Pharmacy, Inc. is recalling a sterile injectable drug product because airflow patterns may not support aseptic production, raising sterility concerns.
Vyaire Medical is recalling 8,124 AirLife Infant Resuscitation devices because the mask may stick to the elbow, making it difficult or impossible to disconnect.