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
Fengrong Tool electric pressure washers are recalled because they lack an integral ground-fault circuit interrupter, posing shock and electrocution hazards. About 500 units are affected.
Multi-point suspension swing frames sold by Fun and Function are recalled because the frame can crack or break during use, posing a fall hazard. Ten failures and two contusions have been reported.
Chrysler is recalling 2026 Ram 2500 trucks because steering column modules may cause a loss of electronic stability control, increasing crash risk.
Manik and Apex-branded ATX computer power supplies are recalled because they lack a permanent on-product label warning of shock and electrocution hazards if the unit is opened.
Roush is recalling 1,217 2026 Nissan Frontier Pro4X R vehicles because steering and suspension fasteners may be loose or missing, posing a crash risk.
Medline is recalling Non Vascular Pack and Vein convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use.
Medline is recalling custom manifold and cryo EP manifold kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use. 1,698 kits are affected.
Fresh whole cantaloupes sold under the Ayco brand are being recalled over potential Salmonella contamination. The action covers 8,302 cartons distributed to four states.
Medline is recalling Robotic Pack and Uro/Gen Robotic Pack convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use.
Medline is recalling Head and Neck CDS-LF and Heart Cath Pack-LF convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect.
Audi is recalling certain 2019-2024 e-tron and Q8 e-tron vehicles because an improperly assembled fastener can cause the brake pedal to detach from the brake booster.
Connecticut Crab Company LLC is recalling crab cakes sold to food service in New York and New Jersey due to potential temperature abuse that may allow growth of Clostridium botulinum.
Medline is recalling GLOVE PACK 7.0 convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind during use and disconnect from the manifold.
Medline is recalling CVOR Angiography Pack-LF convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use. 3,120 kits are affected.
Medline is recalling cath lab and angiography procedure packs containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect. 17,902 kits are affected.
Medline is recalling laparoscopic herniorrhaphy, lap and minor procedure packs containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use.
Medline is recalling Delivery Pack convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind during use and disconnect from the manifold.
Blue Bull Extreme Male Enhancement Supplement is being recalled after FDA analysis revealed the presence of undeclared sildenafil, a prescription drug ingredient not listed on the label.
Medline is recalling Special Procedure Trays containing NAMIC rotating adaptor control syringes because the adaptor can unwind during use and disconnect from the manifold. 762 units are affected.
Medline is recalling a further tranche of NAMIC Angiographic Syringes because the rotating adaptor can unwind during use and disconnect from the manifold. 2,630,369 units are affected.
Fresenius Kabi USA, LLC is recalling certain batches of 0.9% Sodium Chloride Injection due to concerns regarding sterility assurance.
Medline is recalling Minor Plastic-LF convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind during use and disconnect from the manifold.
Red Bull Extreme Male Enhancement Supplement is being recalled after FDA analysis revealed the presence of undeclared sildenafil, a prescription drug ingredient not listed on the label.
Medline is recalling right and left heart catheterization and angiography kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect. 79,843 units are affected.
Medline is recalling Shoulder Arthroscopy and Extremity Pack convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use.