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 deaths or serious injuries are reported, 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
The CLARITY II Laser System by Lutronic is being recalled following reports of devices sparking and popping, which may burn patients during use. The recall affects 1,525 units distributed worldwide.
An implant connection component manufactured by Waldemar Link may experience bushing detachment due to a longitudinal screw fracture. The recall affects 31 units distributed in the United States and internationally.
Waldemar Link is recalling Endo-Model Replacement Plateau implants (Item 15-2836/11) due to potential bushing detachment from the screw shaft caused by longitudinal fracture. Seven units affected worldwide including the US. No injuries reported.
Medartis AG is recalling certain lots of APTUS 2.8 TriLock Screws due to a mix-up with 2.5mm screws. The dimensional error could affect the fit and stability of orthopedic fixation in hand, forearm, shoulder, and foot surgery.
Waldemar Link is recalling Endo-Model Replacement Plateau implants because the bushing could detach from the screw shaft due to a longitudinal fracture. This could compromise implant stability.
Waldemar Link is recalling 3 units of Endo-Model Replacement Plateau orthopedic implants due to potential detachment of the bushing from the screw shaft. The defect results from a longitudinal fracture in the screw.
Waldemar Link recalls its Endo-Model Replacement Plateau due to potential bushing detachment from the screw shaft, which could cause implant failure. Four units were affected and distributed worldwide.
GEM Premier 5000 lab cartridges may eject repeatedly during warm-up, requiring replacement and potentially delaying patient test results. No illnesses or injuries have been reported.
International Life Sciences is recalling Artelon FlexBand Dynamic Matrix augmentation devices due to failed bacterial endotoxin testing. The devices were distributed nationwide and internationally.
Instrumentation Laboratory is recalling GEM Premier 5000 PAK cartridges that may experience increased ejection errors during warm-up, potentially delaying laboratory test results.
Instrumentation Laboratory is recalling GEM PAK cartridges for the GEM Premier 5000 due to increased failures in process control detection during warm-up, which may cause cartridge ejection and delay laboratory test results.
Instrumentation Laboratory is recalling 74 units of GEM Premier 5000 analyzer cartridges that may malfunction during warm-up, causing cartridge ejection and potentially delaying patient test results.
Physio-Control is recalling Infant/Child Reduced Energy Defibrillator Electrodes due to delamination of the electrode material that could affect proper functioning during emergency treatment of pediatric patients.
International Life Sciences recalls Artelon FlexBand Plus surgical devices (Ref 41054, 41057) worldwide due to bacterial endotoxin contamination discovered during testing.
Polski Ogrod Sp. z o.o. is recalling Hortex Mieszanka 9 Spring vegetable mix due to potential glass contamination. The affected product was distributed in Illinois.
CNC Noodle Corporation is recalling China Noodle Co. Steam Noodle packages due to undeclared wheat in the product, which poses a risk to consumers with wheat allergies.
Palmetto Gourmet Foods Inc. is recalling Vegetarian Chicken Flavor Ramen Express because the product contains undeclared Yellow #5 food coloring, a major allergen for some consumers.
Willamette Valley Pie Company is recalling Frozen Raw Bulk 9 inch Blueberry Crumble Pie due to potential contamination with listeria monocytogenes. The frozen pies were sold to grocery retailers' in-store bakeries in Illinois and Oregon.
LFTE USA recalls about 7,200 playground swing set seats with faulty rivets that can fail, causing children to fall. One minor injury has been reported; stop using recalled swings immediately and contact the manufacturer for free replacement.
About 3,000 14-drawer dressers sold online at Wayfair are being recalled because they can tip over and cause entrapment if not anchored to the wall. No injuries have been reported.
LIVEHOM 11-Drawer fabric dressers sold on Amazon are unstable without wall anchoring, creating tip-over and entrapment hazards for children. About 370 units recalled; no injuries reported.
ProRider bicycle helmets fail to meet federal safety standards and may not protect users in crashes. The recall affects about 9,546 helmets sold from June 2022 to May 2023.
Stoney Games recalls Kluster magnet chess games with loose magnets posing serious ingestion hazard to children. No injuries reported to date.
Mojo Max Fusion XXX capsules contain undeclared sildenafil and tadalafil, prescription drugs marketed without FDA approval. All lots (exp. 12/31/2027) distributed nationwide should not be used.
Certain 2022-2024 Jeep Grand Cherokee and 2021-2024 Grand Cherokee L vehicles have an improperly secured front seat side air bag connector that may prevent deployment. Chrysler has remedied all affected vehicles.