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
Honda is recalling certain 2024 Acura ZDX vehicles because stabilizer bar bracket bolts may become loose and damage high voltage cables or EV battery coolant lines, potentially causing loss of drive power and increased crash risk.
Teva Pharmaceuticals is recalling 19,869 cartons of Octreotide Acetate injection due to quality system deficiencies at the manufacturer that affect sterility assurance. The FDA discovered these deficiencies during a routine inspection.
Teva Pharmaceuticals is recalling Octreotide Acetate injectable suspension (30 mg) nationwide due to quality system deficiencies at the contract manufacturer that compromised sterility assurance.
I.T.S. GmbH is recalling FLS and HOL foot locking plates because updated MRI safety testing shows higher RF-induced temperature increases than previously documented. Patients with these implants should consult product instructions before undergoing MRI.
Olympus is recalling PKS Cutting Forceps worldwide due to defective welds in supplier components. The surgical instrument's jaw can break during clinical use.
Teva Pharmaceuticals is recalling Octreotide Acetate injectable suspension nationwide due to quality system deficiencies identified at the contract manufacturer that affect assurance of product sterility.
Olympus Corporation recalled PKS Cutting Forceps due to inadequate welding validation by suppliers, which can cause the device's jaw to break during surgical use.
The I.T.S. Pelvic Reconstruction System implants generate higher MRI-induced heating than documented in instructions. The FDA recalled approximately 46,637 units due to potential thermal injury risk during MRI procedures.
I.T.S. fibula surgical plates may generate higher temperature increases during MRI scans than documented. Updated safety testing revealed the thermal risk under certain MRI conditions.
Straumann USA is recalling 13 Custom Abutment Ti units due to a manufacturing error where the wrong material (TAN) was used instead of titanium. The affected units were distributed nationwide and to Canada.
I.T.S. GmbH is recalling 292 Humeral Head Plates due to inaccurate MRI safety instructions. Updated testing shows RF heating risks are higher than previously documented.
I.T.S. GmbH is recalling Claviculaplate orthopedic implants nationwide due to higher-than-documented radiofrequency-induced temperature increases during MRI scans. Updated MRI safety testing revealed the implants may generate more heat than previously indicated.
The FR.O.H. Calcaneus Repair System has been recalled due to higher-than-documented RF-induced temperature increases during MRI procedures. The manufacturer is updating safety instructions to reflect testing results.
Olympus Corporation is recalling 164 units of Everest Bipolar Cutting Forceps (Model 3006) due to defective welds in components that can cause the jaw to break during surgical use.
Olympus is recalling its PKS Cutting Forceps (Model 920005PK) because components contain defective welds that could cause the forceps' jaw to break during clinical use. Healthcare facilities should discontinue use and contact the manufacturer.
Koven Technology is recalling 34 units of the BiDop 3 Pocket Doppler because the product labeling includes a fetal indication for use that was not cleared by the FDA through the 510(k) pre-market notification process.
I.T.S. GmbH is recalling the Volar Radius Plate with Angular Stability (Radius Plate PROlock II) because updated MRI safety testing shows the device generates higher radiofrequency-induced heat during MRI scans than its Instructions for Use previously indicated.
General Motors is recalling 2025 Chevrolet Equinox EV all-wheel drive vehicles because the adaptive cruise control system may fail to engage the brakes due to incorrect brake module software, increasing crash risk.
Olympus is recalling HALO PKS Cutting Forceps due to inadequate welding validation. Defective welds may cause the device's jaw to break during surgical use.
Beckman Coulter is recalling 685 boxes of MicroScan Neg MIC 56 diagnostic panels due to likely presence of contamination in test wells. The affected lot was distributed across 12 U.S. states.
Land Rover is recalling 2023 Discovery Sport, Defender, and Range Rover Evoque vehicles because the touchscreen may not display the rearview camera image, reducing rear visibility and increasing crash risk.
General Motors is recalling certain 2024–2025 GMC Sierra EV and 2024 Chevrolet Silverado EV vehicles because the bolt securing the rear center seat belt assembly may not be properly tightened, which could result in improper restraint during a crash.
American Laboratories is recalling Pepsin Full Strength Powder (50 kg drums/boxes, Item #5000545) due to potential Salmonella contamination. The product was distributed to wholesale accounts in multiple US states and Australia.
Ajinomoto Foods North America Inc. is recalling Trader Joe's Vegetable Fried Rice (1 lb bags, Item 5650233) due to glass fragments (1–3 cm long, 2–4 mm wide) found in the product. The recall affects approximately 9.9 million pounds distributed across 40 US states.
Ajinomoto Foods North America Inc. is recalling Ajinomoto Vegetable Gyoza Dumplings due to the presence of glass fragments in the product. The recalled dumplings were distributed nationwide.