Latest Product Recalls Today

Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the surface of the catheter. Issue may result in the use of urinary catheters that exhibit staining on the catheter surface; raw material present in increased amounts may be harmful.

Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of Bacillus species.

Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the surface of the catheter. Issue may result in the use of urinary catheters that exhibit staining on the catheter surface; raw material present in increased amounts may be harmful.

Product may experience accelerated roller wear and potential deformation due to interference between the roller assembly and rail. In the worst-case condition, rail mechanism may become lodged during operation and movement of the stretcher along the rail may no longer be possible through either powered or manual operation. May cause delays in transport of patient to healthcare facility.

Labeling discrepancy: Devices distributed with Instructions For Use (IFU) did not include FARAPOINT PFA catheter information.

Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the surface of the catheter. Issue may result in the use of urinary catheters that exhibit staining on the catheter surface; raw material present in increased amounts may be harmful.

Flexible hysteroscopes indicated for use during diagnostic and operative hysteroscopic procedures may contain an expired single use endoscopic seal for gynecology use, which could impact the assurance of sterility.

ICU Medical became aware of an increased likelihood of leakage in specific Lots of L-70 HOTLINE Fluid Warming Sets due to potentially inadequate solvent application at the tubing to return connector bond.

The procedure kits contain ICU Medical, Inc. pain management kits containing Bupivacaine Hydrochloride in Dextrose Injection, USP, which were recalled due to quality issues that could result in drug ineffectiveness.

Labeling discrepancy: Devices distributed with Instructions For Use (IFU) did not include FARAPOINT PFA catheter information.

For MiniMed Go app version 1.0.0 and 1.1.0, when the Set day and night is turned OFF and missed dose or Correct high glucose alerts are enabled, the associated alerts will not be triggered during the nighttime. This could result in missed rapid-acting insulin doses without the user s knowledge, and may lead to delayed therapy and an increased risk of hyperglycemia.

Intraoperative neuromonitoring device, due to a software issue, may experience loss or interruption of triggered electromyography (tEMG) functionality during use, displaying as system faults, loss of communication between the Patient Interface and Tablet, and prompts requiring system reboot; may result in increased operative time and surgical plan change.

Due to manufacturing issues, reperfusion catheters may fractures

Defects in the silicone seal, which may result in "doming" of the silicone seal due to improper sealing, potentially leading to fluid occlusion or leakage.

Boston Scientific is replacing specific FARASTAR PFA generators which have a configuration that is not compatible for use with the FARAPOINT PFA catheter.

Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to dilator insertion orientation during device preparation. Valve damage may result in air ingress, potential air embolism, and associated patient harm. This risk can be mitigated by inserting the dilator straight through the center of the valve and fully advancing it into the sheath body.

Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain side curtain air bag (CSA) assemblies sold as replacement parts for 2016-2023 Toyota Tacoma vehicles. The side curtain air bag may have been improperly secured to its mounting bracket, causing an improper air bag deployment. Improper air bag deployment can increase the risk of injury during a crash.

Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain side curtain air bag (CSA) assemblies sold as replacement parts for 2014-2021 Toyota Tundra Double Cab and CrewMax vehicles. The side curtain air bag may have been improperly rolled, causing an improper air bag deployment. Improper air bag deployment can increase the risk of injury during a crash.

WASHINGTON, Jul 29, 2026 - The U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) is issuing a public health alert for a Steak, Cilantro, Lime Burrito product due to misbranding and an undeclared allergen. The product contains egg, a known allergen, which is not declared on the product label. FSIS is issuing this public health alert to ensure that consumers with allergies to egg products are aware that this product should not be consumed. A recall was not requested because the affected product is no longer available for purchase. The Steak, Cilantro, Lime Burrito product was produced on Jun 19, 2026. The following product is subject to the public health alert [ view labels ]: 3-lb 2-oz. carton containing 10 individually wrapped "RED'S STEAK CILANTRO AND LIME BURRITO" on the front package label with production lots, L1 SD6170 1503, L1 SD6170 1535, L1 SD6170 1606, L1 SD6170 1639, L1 SD6170 1717, L1 SD6170 1750, L1 SD6170 1831, L1 SD6170 1908, L1 SD6170 1954, L1 SD6170 2031, L1 SD6170 2108, L1 SD6170 2130 on the side of the package label. The individual products bear the establishment number "EST. 46069" inside the USDA mark of inspection. These items were shipped to Costco distribution locations in Illinois, Michigan and Minnesota. The problem was discovered by a consumer that identified the product contained in the carton of "RED'S STEAK CILANTRO AND LIME BURRITO" was a different product, which contains egg, and had been incorrectly labeled. The consumer reported the issue to the producing establishment, and the establishment notified FSIS. There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider. FSIS is concerned that some product may be in consumers' freezers. Consumers who have purchased this product are urged not to consume it. The product should be thrown away or returned to the place of purchase. Media and consumers with questions regarding the public health alert can contact Andrea Breen, Chief Supply Chain Officer, Red's All Natural, at 203-437-7713, or [email protected] . Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or send a question via email to [email protected] . For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/ .

Newell Coach Corp. (Newell) is recalling certain 2025-2027 P50 coaches. The steer axle air spring base may crack. A cracked base may result in a loss of air pressure and suspension support, increasing the risk of a crash.

Grand Design RV, LLC (Grand Design) is recalling certain 2026-2027 Lineage motorhomes equipped with the 20-inch wheel and tire package. The tire information label may state the incorrect rear tire pressure. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 120, "Wheels and Rims - Other than Passenger Cars." Incorrect tire pressure information can result in over inflated tires, increasing the risk of tire failure and a crash.

Grand Design RV, LLC (Grand Design) is recalling certain 2027 Imagine recreational trailers. The inverter prep circuit conductor may have insufficient overcurrent protection, causing the conductor to overheat. An overheated conductor may increase the risk of a fire.

Ford Motor Company (Ford) is recalling certain 2023-2025 Mustang Mach E vehicles. The rear side quarter window glass trim may be improperly secured, which can allow it to detach. Detached trim pieces can create a road hazard, increasing the risk of a crash.

Ford Motor Company (Ford) is recalling certain 2021-2023 F-150 and 2023-2026 F-250 SD vehicles equipped with 8-inch SYNC infotainment screens. A software error may cause the rearview camera image to be obstructed by the infotainment home screen menu when the vehicle is placed in reverse. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 111, "Rear Visibility." An obstructed rearview camera image can reduce the driver's rear visibility, increasing the risk of a crash.

Grand Design RV, LLC (Grand Design) is recalling certain 2026 Imagine travel trailers. The outlet cover may have been improperly secured, allowing screws to contact wiring. Contact with wiring may cause a short circuit or an electrical arc, increasing the risk of a fire.