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
Busse Hospital Disposables is recalling Carpal Tunnel Packs because they contained Devon Light Gloves subject to a labeling update.
Ortho-Clinical Diagnostics is recalling VITROS CRP Slides because the diluent contains endogenous CRP, which can cause falsely high test results if not subtracted.
Biomet 3i is recalling 60 units of Low Profile Abutment Quickbridge because some product pouches may not have been sealed during packaging.
OrthoPediatrics is recalling 22 PediNail Intramedullary Nailing System 4.5mm X 48mm Cortical Screws because they measure 50mm instead of the labeled 48mm.
Biomet 3i is recalling 108 low profile abutments because some pouches may not have been sealed during packaging.
Biomet 3i is recalling specific low-profile dental implant abutments because a limited number of product pouches may not have been sealed during packaging.
Biomet 3i is recalling 123 units of Low Profile Dental Abutments because some product pouches may not have been sealed during packaging.
Biomet 3i is recalling 191 dental implant abutments because some product pouches may not have been sealed during packaging.
Biomet 3i is recalling 28 dental implant abutments because some product pouches may not have been sealed during packaging.
Biomet 3i is recalling 204 dental implant abutments because some product pouches may not have been sealed during packaging.
Biomet 3i is recalling 175 dental implant abutments because some product pouches may not have been sealed during packaging.
Biomet 3i is recalling 108 dental implant abutments because some product pouches may not have been sealed during packaging.
Biomet 3i is recalling 191 Low Profile Abutment units because some pouches may not have been sealed during packaging.
Biomet 3i is recalling 458 low profile abutment impression copings because a limited number of product pouches may not have been sealed during packaging.
Biomet 3i is recalling 246 dental implant abutments because a limited number of product pouches may not have been sealed during packaging.
Biomet 3i is recalling 127 dental implant abutments because some product pouches may not have been sealed during packaging.
Biomet 3i is recalling 735 low profile dental abutments because a limited number of product pouches may not have been sealed during packaging.
Biomet 3i is recalling 64 dental implant abutments because some product pouches may not have been sealed during packaging.
Biomet 3i is recalling 1,371 low profile abutments because a limited number of product pouches may not have been sealed during packaging.
Biomet 3i is recalling 137 dental implant abutments because some product pouches may not have been sealed during packaging.
Biomet 3i is recalling 391 Low Profile Abutment Healing Caps because a limited number of product pouches may not have been sealed during packaging.
PerkinElmer is recalling 73 EnLite Neonatal TREC Kits because the Unique Device Identifier (UDI) is missing from the outer box labels.
Biomet 3i is recalling 124 dental implant abutments because some product pouches may not have been sealed during packaging.
Biomet 3i is recalling 450 units of Low Profile One-Piece Abutments because a limited number of product pouches may not have been sealed during packaging.
Biomet 3i is recalling 228 dental implant abutments because a limited number of product pouches may not have been sealed during packaging.