Recent recall alerts · Updated daily

Latest Product Recalls Today

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.

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Search recent recall notices by product name, brand, UPC, lot code, model number, source agency or official recall number.

Recent Product Recall Alerts List

Showing 3,451 - 3,475 of 4,975 matching product recalls.
Product Recall Search
Product Recall Source Type Risk Date Action
FDA Z-1789-2026
Medical Device High
Apr 15, 2026 Recall: Mar 5, 2026
Details
FDA Z-1804-2026
Medical Device High
Apr 15, 2026 Recall: Mar 12, 2026
Details
B.R.A.H.M.S PlGF Plus KRYPTOR, Catalog Number: 859075N. in vitro diagnostic test for Placental Growth Factor
Customers have observed quality control values out of range at the lowest quality control level (QC Level 1) for the PIGF assay which require troubleshooting steps to resolve. If Quality Controls are not performed according to the Instructions for Use, the underestimation of QC1 may go undetected and could contribute to falsely elevated sFlt-1/PlGF ratio results. A falsely elevated sFlt-1/PlGF ratio may result in a higher-risk classification for progression to preeclampsia with severe features potentially leading to intensified clinical monitoring.
FDA Z-1795-2026
Medical Device High
Apr 15, 2026 Recall: Mar 12, 2026
Details
COOK MEDICAL Approach CTO-18 Micro Wire Guide, Reference Part Number CMW-14-190-18G, Order Number G50788; Reference Part Number CMW-14-300-18G, Order Number G50792
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
FDA Z-1777-2026
Medical Device High
Apr 15, 2026 Recall: Mar 5, 2026
Details
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
FDA Z-1780-2026
Medical Device High
Apr 15, 2026 Recall: Mar 5, 2026
Details
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
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
FDA Z-1716-2026
Medical Device High
Apr 15, 2026 Recall: Feb 27, 2026
Details
FDA Z-1713-2026
Medical Device High
Apr 15, 2026 Recall: Feb 27, 2026
Details
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
Showing 3,451 - 3,475 of 4,975 product recalls

Product Recalls Today

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High-Risk Recall Updates

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Daily Official Source Coverage

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Latest Recalls By Source Agency

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CPSC

Latest Consumer Product Recalls

New alerts for toys, furniture, appliances, electronics, baby products, household goods and products with injury, choking, fire or fall hazards.

FDA

Latest Food And Medical Device Recalls

Recent FDA notices can include Class I, Class II and Class III recalls, market withdrawals, safety alerts, code information and distribution areas.

USDA FSIS

Latest Meat And Poultry Recall Alerts

FSIS alerts cover meat, poultry and egg products, including public health alerts, undeclared allergens, pathogen risks and misbranding issues.

NHTSA

Latest Vehicle Recall Campaigns

New vehicle, tire, equipment and child-seat campaigns include defect summaries, affected units, remedy notes and NHTSA campaign numbers.

How To Use The Latest Product Recalls Page

Check The Publish Date First

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Filter By Product Type

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Prioritize High-Risk Notices

Sort by highest risk when checking for urgent problems such as contamination, serious injury hazards, undeclared allergens, fire risks or vehicle safety defects.

Verify The Official Notice

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.

Latest Product Recalls FAQ

Helpful context for searches such as product recalls today, recent product recalls and recall alerts.

How often is the latest product recall list updated?

The site syncs official recall sources daily and stores updated records by source agency, dataset and official recall ID.

Why do some recent recalls have older recall dates?

Some agencies publish or classify a recall after the company began the recall. Use both the published date and recall date when reviewing a notice.

What should I check on a recent food recall?

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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Yes. Use the risk filter or highest-risk sort to surface recalls marked critical or high risk across all official sources.