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 |
|
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 |
|
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 |
|
Incorrect Weight Capacity on Label/FMVSS 110
Bentley Motors, Inc. (Bentley) is recalling certain 2026 Bentayga vehicles. The maximum vehicle capacity weight value on the tire placard label is incorrect. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 110, "Tire Selection and Rims." Incorrect weight information may lead to unintentionally overloading the vehicle, increasing the risk of a crash.
|
NHTSA
26V231000
|
Vehicle | High |
Apr 10, 2026
Recall: Apr 10, 2026
|
Details |
Yeeluzan Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by Yeeluzan
This recall involves Yeeluzan-branded pool drain covers that are sold for use in swimming pools. The pool drain covers measure about 8.7 inches in diameter and weigh 1.7 pounds. They are white and made of ABS plastic and sold in two-packs.
|
CPSC
10704
|
Consumer Product | High |
Apr 10, 2026
Recall: Apr 9, 2026
|
Details |
Vitaquest International Recalls Multiple Iron Supplement Bottles and Packets Due to Risk of Serious Injury or Death from Poisoning to Young Children; Violates Mandatory Standard for Child-Resistant Packaging
This recall involves Arey, Bari Life, Bird&Be, Biote, Dr. Fuhrman, NuLife, HMR, Bariatric Pal, Noevir, Zenbean and Sakara brand iron-containing dietary supplements without child-resistant packaging. Brand / Product Name Arey Not Today, Grey (60ct and 180ct) 0034I5 Sept. 2027 860007168901 0342B5 Feb. 2027 860007168901 0342B5A Feb. 2027 860007168901 0360G5 July 2027 860007168901 0442H4 Sept. 2026 860007168994 0442H4A Sept. 2026 860007168994 0442H4B Sept. 2026 860007168994 0483G5 July 2027 860007168994 Bari Life Complete Bariatric Vitamin - Watermelon (60ct) 0138G5 July 2028 860012913930 0177D3 April 2026 860012913930 0207A4 Jan. 2027 860012913930 0333K4 Nov. 2027 860012913930 Bird&Be The Prenatal Essentials for Females (30 pkts) 0005K4 Oct. 2026 860010126417 Bird&Be The Power Prenatal for Females (30 pkts) 0006K4 Aug. 2026 860010126479 Bird&Be The Power Prenatal for Females + CoQ10 Boost (30pkts) 0060L4 Aug. 2026 860010126493 Bird&Be Female Fertility Power Prenatal Pack (30 pkts) 0346C5 March 2027 860013460136 0354F5 May 2027 Bird&Be Complete Prenatal Pack (30 pkts) 0342C5 May 2027 860013460174 0345F5 0345F5A 0345F5B Bird&Be Female Fertility Power Prenatal + CoQ10 Pack (30 pkts) 0360F5A June 2027 860013460143 0360F5 June 2027 0350C5 March 2027 Biote Nutraceutical Iron+ (30ct) 0068F5 May 2027 0516K4 0516K4 Jan. 2027 0068F5 Dr. Fuhrman Gentle Prenatal Multivitamin + D3 (120ct) 0091A5 Feb. 2027 829584500061 Dr. Fuhrman Pixie Vites Children's Multivitamin (120ct) 0130K4 Dec. 2026 829584500153 NuLife Advanced Bariatrics Multivitamin Chewable Tablets (60ct) 0041C4 Feb. 2027 746888915028 0248J4 Oct. 2027 746888915028 0248J4A Oct. 2027 746888915028 0305F5 July 2027 746888915028 0342J3 Oct. 2026 746888915028 0363F3 June 2026 746888915028 0363F3A June 2026 746888915028 0416C5 April 2027 746888915028 0440H4 Sept. 2027 746888915028 0521D5 May 2027 746888915028 HMR Multi Daily Vitamin and Mineral Supplement (60ct) 0013H5 July 2027 00709355144413 Bariatric Pal Ultra Multi Bariatric Multivitamin (90ct) 0148I4 Sept. 2026 0038407566232 Noevir Inner Care Premium BioEssentials (120ct) 0134F4 July 2026 N/A Zenbean Kids Café Instant Coffee + Nutrition Latte, Original, Caramel, Chocolate, and Vanilla (30srv) 0028H4 Aug. 2026 810067444910 0051H5 Aug. 2028 850067341338 0052H5 Aug. 2028 850067341314 0050H5 Aug. 2028 850067341321 Sakara The Foundation (30pkts) 0340A5 Sept. 2026 858151008334 0340A5A Sept. 2026 858151008334 0340A5B Sept. 2026 858151008334 0340A5C Feb. 2027 858151008334 0340A5D Feb. 2027 858151008334 0540H4D June 2026 858151008334 Sakara The Foundation: Prenatal (30pkts) 0338A5A Feb. 2027 858151008341 0338A5B Feb. 2027 858151008341.
|
CPSC
10695
|
Child/Baby | High |
Apr 10, 2026
Recall: Apr 9, 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.
This latest recall page combines CPSC, FDA, USDA FSIS and NHTSA data so shoppers do not need to check each agency page separately.
New alerts for toys, furniture, appliances, electronics, baby products, household goods and products with injury, choking, fire or fall hazards.
Recent FDA notices can include Class I, Class II and Class III recalls, market withdrawals, safety alerts, code information and distribution areas.
FSIS alerts cover meat, poultry and egg products, including public health alerts, undeclared allergens, pathogen risks and misbranding issues.
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Choose food, vehicle, medical device, baby product, electronics, household or consumer product when the latest list is too broad.
Sort by highest risk when checking for urgent problems such as contamination, serious injury hazards, undeclared allergens, fire risks or vehicle safety defects.
Use the detail page and official source link before taking action. Agency notices may include exact lot codes, model ranges, remedy steps and company contacts.
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Match the brand, product name, package size, UPC, lot code, best-by date, allergen or contamination issue and distribution area before taking action.
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