Product Recalls Today
Use the Today filter when you want newly published recall alerts from the current U.S. date. If no results appear, check the last 7 or 10 days because agencies may publish updates in batches.
Track recent product recall alerts from official U.S. sources. Filter by recall date, source agency, risk level and product category to find newly published food, vehicle, baby product, medical device and consumer product recalls.
Search recent recall notices by product name, brand, UPC, lot code, model number, source agency or official recall number.
| Product Recall | Source | Type | Risk | Date | Action |
|---|---|---|---|---|---|
|
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. MTO,SYRINGE,12ML,TR/FG,RA,W/RES, Medline SKU 70087107; 6. SYRINGE,12ML,TR/FR,RA,W/O,RES,-,PKG, Medline SKU 70088007; 7. SYRINGE,10ML,PP/FR,RA,-,PKG, Medline SKU 70095007; 8. SYRINGE,10ML,PP/FG,RA,-,PKG, Medline SKU 70095107; 9. SYRINGE,12ML,W/RES,PP/FR,RA,PG, Medline SKU 70097007; 10. SYRINGE,12ML,PP/FG,RA,W/RES,-,PKG, Medline S
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
|
FDA
Z-1712-2026
|
Medical Device | High |
Apr 15, 2026
Recall: Feb 27, 2026
|
Details |
|
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. ROBOTIC PACK, Medline SKU # DYNJ58475F; 2. URO/GEN ROBOTIC PACK, Medline SKU # DYNJ60803J.
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
|
FDA
Z-1728-2026
|
Medical Device | High |
Apr 15, 2026
Recall: Feb 27, 2026
|
Details |
|
COOK MEDICAL Blue Rhino¿ G2-Multi Percutaneous Tracheostomy Introducer Tray: Reference Part Number C-PTISY-100-HC-G-NA, Order Number G57703; Reference Part Number C-PTISY-100-UNL-HC-G-NA, Order Number G57706; Reference Part Number C-PTISY-100-UNS-HC-G-NA, Order Number G57704.
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
|
FDA
Z-1780-2026
|
Medical Device | High |
Apr 15, 2026
Recall: Mar 5, 2026
|
Details |
|
COOK MEDICAL Wayne Pneumothorax Set: Reference Part Number C-UTPT-1020-WAYNE-IMH, Order Number G56532; Reference Part Number C-UTPT-1400-WAYNE-112497-IMH, Order Number G56535.
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
|
FDA
Z-1791-2026
|
Medical Device | High |
Apr 15, 2026
Recall: Mar 5, 2026
|
Details |
|
COOK MEDICAL Cook¿ Strange Bile Duct Stone Exploration Set: Reference Part Number C-CSRC-7.5D-40-STRANGE, Order Number G09108
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
|
FDA
Z-1784-2026
|
Medical Device | High |
Apr 15, 2026
Recall: Mar 5, 2026
|
Details |
|
Melker Universal Cuffed Emergency Cricothyrotomy Catheter Set: Reference Part Number C-TCCSB-500-UNI, Order Number G32193; Reference Part Number C-TCCSB-500-UNI-01, Order Number G47665.
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
|
FDA
Z-1785-2026
|
Medical Device | High |
Apr 15, 2026
Recall: Mar 5, 2026
|
Details |
|
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: SPECIAL PROCEDURE TRAY, Medline SKU # DYNJ80513B
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
|
FDA
Z-1720-2026
|
Medical Device | High |
Apr 15, 2026
Recall: Feb 27, 2026
|
Details |
|
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: CVOR ANGIOGRAPHY PACK-LF, Medline SKU DYNJ42367B
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
|
FDA
Z-1714-2026
|
Medical Device | High |
Apr 15, 2026
Recall: Feb 27, 2026
|
Details |
|
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. CATH LAB PACK-LF, Medline SKU 00-HCT055P; 2. INTERVENTIONAL CATH LAB PK-LF, Medline SKU DYNJ0376230Q; 3. ANGIOGRAPHY CATH LAB, Medline SKU DYNJ23532C; 4. ANGIO LEFT HEART PACK, Medline SKU DYNJ40632C; 5. ANGIO DRAPE PACK, Medline SKU DYNJ47952B; 6. ANGIOGRAPHIC PACK, Medline SKU DYNJ57516; 7. CATH LAB PACK, Medline SKU DYNJ58243B; 8. CATH LAB PACK, Medline SKU DYNJ65185; 9. CSU CATH MANIFOLD KIT, Medline SKU VASC1170A; 10. MANIFOLD KIT NO TRANSDUCER
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
|
FDA
Z-1716-2026
|
Medical Device | High |
Apr 15, 2026
Recall: Feb 27, 2026
|
Details |
|
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. SYRINGE,7,ML,TR/FR,RA,W/RES,OEM,PG, Medline SKU 80083007; 5. SYRINGE,8,ML,TR/FR,RA,W/RES,OEM,PG, Medline SKU 80084007; 6. MTO,SYRINGE,8,ML,TR/FR,RA,NO,RES,OEM,PG, Medline SKU 80084017.
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
|
FDA
Z-1713-2026
|
Medical Device | High |
Apr 15, 2026
Recall: Feb 27, 2026
|
Details |
|
COOK MEDICAL Arterial Pressure Monitoring Tray, Reference Part Number APMY-2.5-15-0-2.5 , Order Number G58412; Reference Part Number APMY-4.0-21J-1-12, Order Number G58419
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
|
FDA
Z-1778-2026
|
Medical Device | High |
Apr 15, 2026
Recall: Mar 5, 2026
|
Details |
|
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.
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
|
FDA
Z-1719-2026
|
Medical Device | High |
Apr 15, 2026
Recall: Feb 27, 2026
|
Details |
|
XTANT MEDICAL Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm, Part Number X073-6555-DL.
Units from one lot were mislabeled with an incorrect part number, identifying the device as a shorter screw length than it physically is.
|
FDA
Z-1773-2026
|
Medical Device | High |
Apr 15, 2026
Recall: Feb 18, 2026
|
Details |
|
Brake Pedal May Detach from Brake Booster
Volkswagen Group of America, Inc. (Audi) is recalling certain 2019-2023 Audi E-Tron Quattro, 2020-2023 Audi E-Tron Sportback, 2024 Q8 E-Tron, Q8 Sportback E-Tron, SQ8 E-Tron, and SQ8 Sportback E-Tron vehicles. The fastener that connects the brake pedal and the brake booster may have been improperly assembled during manufacturing, which can cause the brake pedal to detach from the brake booster. Brake pedal detachment can cause a loss of brake function and increase the risk of a crash.
|
NHTSA
26V240000
|
Vehicle | High |
Apr 15, 2026
Recall: Apr 15, 2026
|
Details |
|
Missing Side Reflectors/FMVSS 108
Winnebago Industries, Inc. (Winnebago) is recalling certain 2027 Suncruiser and 2026-2027 Sunflyer motorhomes. The side reflectors may not have been installed. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 108, "Lamps, Reflective Devices, and Associated Equipment." Missing reflectors can reduce the visibility of the vehicle to other drivers, increasing the risk of a crash.
|
NHTSA
26V241000
|
Vehicle | High |
Apr 15, 2026
Recall: Apr 15, 2026
|
Details |
|
Do Not Drive: Loss of Steering Control from Loose or Missing Fasteners
Roush Performance Products, Inc. (Roush) is recalling certain 2026 Nissan Frontier Pro4X R vehicles. The cotter pins for the upper control arm ball joint and steering tie rod ends may not have been installed, and fasteners may not be properly tightened. Loose or missing fasteners can cause a loss of vehicle steering and control, increasing the risk of a crash.
|
NHTSA
26V242000
|
Vehicle | Critical |
Apr 15, 2026
Recall: Apr 15, 2026
|
Details |
|
Missing Front Axle Hub Spindle Nut
Ford Motor Company (Ford) is recalling certain 2025-2026 F-59 and F-53 vehicles. The front axle hub assembly may be missing the spindle nut and cotter pin. A missing spindle nut may lead to brake system damage or wheel detachment, resulting in a loss of vehicle control and increasing the risk of a crash.
|
NHTSA
26V235000
|
Vehicle | High |
Apr 14, 2026
Recall: Apr 14, 2026
|
Details |
|
Loss of Drive Power due to Transmission Misalignment
Ford Motor Company (Ford) is recalling certain 2021-2025 Bronco vehicles. The transmission to transfer case joint may be misaligned due to an incorrectly performed previous repair, which could lead to wear of the transmission output shaft splines and transfer case input splines. Excessive wear of the transmission and transfer case splines may result in a loss of drive power or vehicle rollaway, increasing the risk of a crash.
|
NHTSA
26V236000
|
Vehicle | High |
Apr 14, 2026
Recall: Apr 14, 2026
|
Details |
|
Unexpected Downshift Can Cause Loss of Control
Ford Motor Company (Ford) is recalling certain 2015-2017 F-150 vehicles. A loss of signal between the transmission range sensor and the powertrain control module can cause the transmission to unexpectedly downshift into second gear. Unexpectedly downshifting into second gear may result in a loss of vehicle control, increasing the risk of a crash.
|
NHTSA
26V237000
|
Vehicle | High |
Apr 14, 2026
Recall: Apr 14, 2026
|
Details |
|
Sun Visor Wiring May Cause Fire
Ford Motor Company (Ford) is recalling certain 2024-2026 Ranger vehicles. The sun visor or headliner wiring harnesses may be improperly positioned or have excessive tape thickness, which can result in damaged wires. Damaged wires can create an electrical short and cause a fire in the A-pillar area, increasing the risk of injury or a crash.
|
NHTSA
26V238000
|
Vehicle | High |
Apr 14, 2026
Recall: Apr 14, 2026
|
Details |
|
Block Heater May Overheat and Cause Fire
Ford Motor Company (Ford) is recalling certain 2025 Maverick and 2026 Bronco Sport vehicles equipped with a 1.5L or 2.0L MPC engine and an engine block heater. The engine block heater may overheat when the vehicle is parked with the block heater plugged in. An overheated engine block heater can increase the risk of a fire.
|
NHTSA
26V239000
|
Vehicle | Unknown |
Apr 14, 2026
Recall: Apr 14, 2026
|
Details |
|
Incorrect Seating Capacity on Label/FMVSS 110
Jayco, Inc. (Jayco) is recalling certain 2025-2026 Entegra Ethos recreational vehicles. The Occupant and Cargo Carrying Capacity (OCCC) and Tire Loading Information labels state an incorrect number of seat belt equipped seating positions, which can result in unbelted passengers. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 110, “Tire Selection and Rims.” Unbelted passengers may not be properly restrained in a crash, increasing their risk of injury.
|
NHTSA
26V233000
|
Vehicle | High |
Apr 13, 2026
Recall: Apr 13, 2026
|
Details |
|
Loss of Rear Brakes
Harley-Davidson Motor Company (Harley-Davidson) is recalling certain 2025-2026 FLHC, FXBB, FXLRS, and FXLRST Softail motorcycles. The rear brake line may contact the Body Control Module (BCM), resulting in a hole in the brake line, a brake fluid leak, and loss of the rear brakes. Loss of the rear brakes increases the risk of a crash.
|
NHTSA
26V234000
|
Vehicle | High |
Apr 13, 2026
Recall: Apr 13, 2026
|
Details |
|
Air Bag Inflator May Rupture or Detach from Steering Wheel
Nissan North America, Inc. (Nissan) is recalling certain 2009-2010 Cube vehicles. The driver’s air bag inflator may rupture or detach from the steering wheel during air bag deployment. A driver's air bag that ruptures or detaches can strike the driver or other occupants, increasing the risk of injury during a crash.
|
NHTSA
26V230000
|
Vehicle | High |
Apr 10, 2026
Recall: Apr 10, 2026
|
Details |
|
Fuel Leak at Pipe Connection
Hyundai Motor America (Genesis) is recalling certain Genesis 2022-2026 GV70, 2023-2025 G90, 2021-2025 G80, and GV80 vehicles. Fuel may leak at the pipe connection between the fuel pipe and fuel rail. A fuel leak increases the risk of a fire.
|
NHTSA
26V229000
|
Vehicle | Unknown |
Apr 10, 2026
Recall: Apr 10, 2026
|
Details |
Use the Today filter when you want newly published recall alerts from the current U.S. date. If no results appear, check the last 7 or 10 days because agencies may publish updates in batches.
Recent recalls can include new notices, updated classifications, expanded lots, changed risk levels and public health alerts. Sort by newest first for the live recall feed view.
High-risk notices often involve serious injury, contamination, undeclared allergens, vehicle crash hazards, fire risks or products that should not be used or consumed.
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New alerts for toys, furniture, appliances, electronics, baby products, household goods and products with injury, choking, fire or fall hazards.
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