Recalls

All US Product 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.

How to read this listing

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.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

1276–1300 of 39697

SevereFDA (Devices)·Z-1713-2026·2026-04-15
NAMIC angiographic control syringes recalled over rotating adaptor unwinding
Medline is recalling NAMIC Angiographic Control Syringes because the rotating adaptor can unwind during use, causing a loose connection or full disconnection from the manifold. 192,690 units are affected.
Product
NAMIC Angiographic Control Syringe, labeled as follows: 1. SYRINGE,7ML,TR/FR,RA,W/RES,-,P/G, Medline SKU 70083007; 2. SYRINGE,8ML,TR/FR,RA,W/RES,-,P/G, Medline SKU 70084007; 3. MTS,SYRINGE,8ML,TR/FR,RA,NO,RES,-,P/G, Medline SKU 70084017; 4.…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V242000·2026-04-15
Roush Nissan Frontier Pro4X R Recalled for Steering Fastener Defect
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.
Product
ROUSH — ROUSH NISSAN FRONTIER PRO4X R
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·H-0655-2026·2026-04-15
Red Bull male enhancement supplement pouches contain undeclared sildenafil
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.
Product
Red Bull Extreme Male Enhancement Supplement, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage: Consume Entire Pouch 30 Minutes before Intercourse. Produced by Red Bull Corporation. Turkey www.redbullhoney.com UPC Code 9554100205595
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-1730-2026·2026-04-15
Medline arthroscopy and extremity packs recalled over syringe adaptor unwinding
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.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. SHOULDER ARTHROSCOPY PACK, Medline SKU # DYNJ30880M; 2. EXTREMITY PACK, Medline SKU # DYNJ64295A.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0654-2026·2026-04-15
Blue Bull male enhancement supplement pouches contain undeclared sildenafil
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.
Product
Blue Bull Extreme Male Enhancement Supplement, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage: Consume Entire Pouch 30 Minutes before Intercourse. Produced by Blue Bull Corporation Made In USA. UPC Code 707443349917
Category
Food
Distribution
1 state
SevereFDA (Food)·H-0656-2026·2026-04-15
Crab Cakes Sold to Food Service Recalled for Botulism Risk
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.
Product
Crab Cakes various sizes sold to food service
Category
Food
Distribution
2 states
SevereFDA (Devices)·Z-1718-2026·2026-04-15
NAMIC angiographic syringes recalled in the largest rotating adaptor action
Medline is recalling NAMIC Angiographic Syringes across multiple sizes because the rotating adaptor can unwind during use and disconnect from the manifold. 1,752,096 units are affected.
Product
NAMIC Angiographic Syringe, labeled as follows: 1. SYRINGE,20ML,CONTROL,-,PKG, Medline SKU 70075027; 2. SYRINGE,10ML,TR/FR,RA,W/RES, Medline SKU 70085007; 3. MTO,SYRINGE,10ML,TR/FG,RA,-,PKG, Medline SKU 70085107; 4. SYRINGE,12ML,TR/FR,RA,W/RES, Medline SKU 70087007; 5.…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1717-2026·2026-04-15
Additional NAMIC angiographic syringe lots recalled over adaptor unwinding
Medline is recalling a further group of NAMIC Angiographic Syringe lots because the rotating adaptor can unwind during use and disconnect from the manifold. 149,439 units are affected.
Product
NAMIC Angiographic Syringe, labeled as follows: 1. SYRINGE,20ML,CONTROL,-,PKG, Medline SKU 70075027; 2. SYRINGE,10ML,TR/FR,RA,W/RES, Medline SKU 70085007; 3. MTO,SYRINGE,10ML,TR/FG,RA,-,PKG, Medline SKU 70085107; 4. SYRINGE,12ML,TR/FR,RA,W/RES, Medline SKU 70087007; 5.…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0653-2026·2026-04-15
Boner Bears Honey Male Enhancement contains undeclared pharmaceutical drugs
Pure Vitamins and Natural Supplements, LLC is recalling Boner Bears Honey Male Enhancement because FDA testing found undeclared sildenafil and tadalafil, prescription drugs not listed on the label.
Product
Boner Bears Honey Male Enhancement 100% Wildflower Honey, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage: Consume 1 entire pouch 30 minutes before Intercourse. MANUFACTURED IN: FLORIDA. UPC 788362191603
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-1719-2026·2026-04-15
Medline non-vascular and vein packs recalled over syringe adaptor defect
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.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. NON VASCULAR PACK, Medline SKU # DYNJ68037C; 2. VEIN, Medline SKU # DYNJ89845; 3. VEIN, Medline SKU # DYNJ89845A.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V240000·2026-04-15
Audi e-tron brake pedal may detach from the brake booster
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.
Product
AUDI — AUDI E-TRON SPORTBACK, E-TRON QUATTRO, Q8 SPORTBACK E-TRON, SQ8 E-TRON
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1724-2026·2026-04-15
Medline cardiac catheterization kits recalled over syringe adaptor unwinding
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.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. MTS RH LFT HRT KIT, Medline SKU # 60010508; 2. MTS 3V W/GUIDE, Medline SKU # 60100701; 3. ANGIOGRAPHY KIT, Medline SKU #…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V238000·2026-04-14
Ford Recalls 2024-2026 Rangers for Sun Visor Wiring Fire Risk
Ford is recalling 2024-2026 Ranger vehicles because improperly positioned sun visor or headliner wiring harnesses may cause an electrical short and fire in the A-pillar area.
Product
FORD — FORD RANGER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V235000·2026-04-14
Ford F-59 front axle hub may be missing its spindle nut
Ford is recalling certain 2025-2026 F-59 and F-53 vehicles because the front axle hub assembly may be missing the spindle nut and cotter pin, which can lead to wheel detachment.
Product
FORD — FORD F-59, F-53
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V237000·2026-04-14
Ford Recalls 2015-2017 F-150 Trucks for Transmission Software Defect
Ford is recalling 2015-2017 F-150 vehicles because a signal loss can cause unexpected downshifting, increasing crash risk. Dealers will update software free of charge.
Product
FORD — FORD F-150
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V236000·2026-04-14
Ford Bronco transfer case joint misalignment may wear driveline splines
Ford is recalling certain 2021-2025 Bronco vehicles because a misaligned transmission to transfer case joint can wear the splines, potentially causing loss of drive power or rollaway.
Product
FORD — FORD BRONCO
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V234000·2026-04-13
2025–2026 Harley-Davidson Softail motorcycles rear brake line defect
Harley-Davidson is recalling certain 2025–2026 Softail motorcycles because the rear brake line may contact the Body Control Module, causing a brake fluid leak and loss of rear brakes. Loss of rear brakes increases crash risk.
Product
HARLEY-DAVIDSON — HARLEY-DAVIDSON FLHC, FXBB, FXLRS, FXLRST
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V228000·2026-04-09
Thomas Built Buses Recalls Saf-T-Liner C2 School Buses for Software Defect
Daimler Trucks North America is recalling 2024-2027 Thomas Built Buses Saf-T-Liner C2 school buses because a software defect may prevent warning lights and the stop sign arm from activating.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26E019000·2026-04-09
Nova Bus Recalls Ricon Hidden Frame Windows for Detachment Risk
Nova Bus is recalling Ricon hidden frame windows sold through Prevost due to inadequate adhesion that may cause glass to detach, increasing crash injury risk.
Product
VISIBILITY:GLASS, SIDE/REAR:CRITICAL FASTENERS recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V226000·2026-04-09
IC Bus Recalls EVSB School Buses Due to High Voltage Switch Defect
International Motors is recalling 2022-2027 IC Bus EVSB school buses because a high voltage disconnect switch may fail to shut off power, posing a risk of electrical shock.
Product
IC BUS — IC BUS EVSB
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·26385·2026-04-09
BISSELL steam cleaner attachments can detach and expel hot water
BISSELL Steam Shot OmniReach and Omni handheld steam cleaners are recalled after 206 reports of hot water or steam escaping from the attachments, including 161 reports of burn injuries.
Product
Steam Shot OmniReach and Steam Shot Omni Steam Cleaners with attachments
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26372·2026-04-09
Osprey robotic pool vacuum batteries can overheat and catch fire
Osprey 700 Max and S1 robotic pool vacuums are recalled because the lithium-ion battery can overheat. Ten reports of overheating or fire have caused nine incidents of property damage; no injuries reported.
Product
Osprey 700 Max and S1 robotic pool vacuums
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·26V230000·2026-04-09
Nissan Recalls 2009-2010 Cube Vehicles Due to Driver Air Bag Defect
Nissan is recalling 2009-2010 Cube vehicles because the driver's air bag inflator may rupture or detach during deployment, posing an injury risk.
Product
NISSAN — NISSAN CUBE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V227000·2026-04-09
Honda Odyssey side air bags may deploy unexpectedly from software error
Honda is recalling certain 2018-2022 Odyssey vehicles because a software programming error can cause the side and side curtain air bags to deploy unexpectedly. 440,830 vehicles are affected.
Product
HONDA — HONDA ODYSSEY
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1647-2026·2026-04-08
Trilogy Evo O2 obstruction alarm may take up to four breaths
Philips Respironics is recalling the Trilogy Evo O2 ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.
Product
Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator device.
Category
Medical Device
Distribution
Distributed nationwide

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1276–1300 of 39697