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Latest Product Recalls Today

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Recent Product Recall Alerts List

Showing 1,426 - 1,450 of 4,622 matching product recalls.
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Product Recall Source Type Risk Date Action
Hotline Fluid Warming Set, single use device, is designed to warm blood and intravenous fluids and deliver them to the patient's intravenous access site at normothermic temperatures under gravity flow conditions, List Number L-70
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.
FDA Z-2759-2026
Medical Device High
Jul 29, 2026 Recall: Jun 24, 2026
Details
MEDLINE medical procedure convenience kit labeled as: 1) TOTAL KNEE-LF, Medline kit SKU CDSOPT590T; 2) TOTAL KNEE-LF, Medline kit SKU CDSOPT590U; 3) TOTAL KNEE CDS, Medline kit SKU CDS983930J; 4) HIP CDS-LF, Medline kit SKU CDS984556L; 5) HIP CDS-LF, Medline kit SKU CDS984556M; 6) TOTAL KNEE PACK, Medline kit SKU DYNJ905162Q.
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.
FDA Z-2765-2026
Medical Device High
Jul 29, 2026 Recall: Jun 8, 2026
Details
FARASTAR Ablation Generator EU, Pulsed Field Ablation Generator, Product ID 61M401; Percutaneous Cardiac Ablation Catheter
Labeling discrepancy: Devices distributed with Instructions For Use (IFU) did not include FARAPOINT PFA catheter information.
FDA Z-2750-2026
Medical Device High
Jul 29, 2026 Recall: Jun 11, 2026
Details
MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)
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.
FDA Z-2778-2026
Medical Device High
Jul 29, 2026 Recall: Jun 16, 2026
Details
SafeOp Patient Interface, REF: AIX11240, part of SafeOp 3: Neural Informatix System
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.
FDA Z-2793-2026
Medical Device High
Jul 29, 2026 Recall: May 13, 2026
Details
Penumbra System RED 68 Reperfusion Catheter REF: RED68KIT
Due to manufacturing issues, reperfusion catheters may fractures
FDA Z-2770-2026
Medical Device High
Jul 29, 2026 Recall: Jun 3, 2026
Details
Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01. Convenience kit.
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.
FDA Z-2772-2026
Medical Device High
Jul 29, 2026 Recall: May 19, 2026
Details
FARASTAR Ablation Generator EU, Pulsed Field Ablation Generator, Product ID 61M401; Percutaneous Cardiac Ablation Catheter
Boston Scientific is replacing specific FARASTAR PFA generators which have a configuration that is not compatible for use with the FARAPOINT PFA catheter.
FDA Z-2753-2026
Medical Device High
Jul 29, 2026 Recall: Jun 11, 2026
Details
FARADRIVE STEERABLE SHEATH CLEAR, used to facilitate access to the vasculature and into the chambers of the heart, Material Number 21M402, IFU Reference Number LBL1062
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.
FDA Z-2755-2026
Medical Device High
Jul 29, 2026 Recall: Jun 11, 2026
Details
Side Curtain Air Bag May Deploy Improperly
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.
NHTSA 26E050000
Vehicle High
Jul 29, 2026 Recall: Jul 29, 2026
Details
Side Curtain Air Bag May Deploy Improperly
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.
NHTSA 26E051000
Vehicle High
Jul 29, 2026 Recall: Jul 29, 2026
Details
Steer Axle Air Springs Base May Crack
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.
NHTSA 26V488000
Vehicle High
Jul 28, 2026 Recall: Jul 28, 2026
Details
Incorrect Tire Pressure Information on Label/FMVSS 120
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.
NHTSA 26V491000
Vehicle High
Jul 28, 2026 Recall: Jul 28, 2026
Details
Window Glass Trim Pieces May Detach
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.
NHTSA 26V487000
Vehicle High
Jul 28, 2026 Recall: Jul 28, 2026
Details
Obstructed Rearview Camera Image/FMVSS 111
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.
NHTSA 26V489000
Vehicle High
Jul 28, 2026 Recall: Jul 28, 2026
Details
Oil Contaminated Power Distribution Center/FMVSS 103
PACCAR Incorporated (PACCAR) is recalling certain 2027 Peterbilt and Kenworth vehicles. Please see the recall report for a complete list of models. The power distribution center (PDC) box may be contaminated with oil, which could result in a loss of drive power, Antilock Brake System (ABS) functionality, exterior lighting, windshield wipers, or the defogging system. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard numbers 103, "Windshield Defrosting and Defogging Systems," 104, "Windshield Wiping and Washing Systems," and 108, "Lamps, Reflective Devices, and Associated Equipment." A loss of lighting, windshield wipers, ABS function, or a loss of drive power can increase the risk of a crash.
NHTSA 26V485000
Vehicle High
Jul 27, 2026 Recall: Jul 27, 2026
Details
Unintended Brake Light Illumination/FMVSS 108
Jayco, Inc. (Jayco) is recalling certain 2025 Entegra Reatta XL, Reatta, 2026 Cornerstone Reserve, 2024-2026 Cornerstone, Aspire, and Anthem motorhomes built on certain Spartan K1, K2, and K4 chassis. The exterior brake lights may remain illuminated when the driver is not applying the brakes. 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." Brake lights that remain on may fail to alert other vehicles of the driver's intention, increasing the risk of a crash.
NHTSA 26V484000
Vehicle High
Jul 27, 2026 Recall: Jul 27, 2026
Details
Unintended Brake Light Illumination/FMVSS 108
Foretravel, Inc. (Foretravel) is recalling certain 2025-2027 Realm Presidential motorcoaches. The exterior brake lights may remain illuminated when the driver is not applying the brakes. 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." Brake lights that remain on may fail to alert other vehicles of the driver's intention, increasing the risk of a crash.
NHTSA 26V486000
Vehicle High
Jul 27, 2026 Recall: Jul 27, 2026
Details
Incorrect Tire Size on Certification Label
Jayco, Inc. (Jayco) is recalling certain 2026 Entegra Anthem motorhomes. The tire size may be incorrect on the vehicle certification label. As such, these vehicles fail to comply with the requirements of 49 CFR Part 567, "Certification." Incorrect information may result in the wrong sized replacement tires being installed, increasing the risk of a crash.
NHTSA 26V483000
Vehicle High
Jul 27, 2026 Recall: Jul 27, 2026
Details
Rollaway Risk from Door Switch Failure
Mercedes-Benz USA, LLC (MBUSA) is recalling certain 2020-2021 CLA, 2019-2022 A-Class, 2022-2023 C-Class, 2024 CLE, 2020-2026 GLA/GLB, and 2023-2024 GLC vehicles. Please refer to MBUSA's recall report for specific model information. The micro-switch in the driver's door lock may corrode and fail to detect an open door, preventing the electronic parking brake or "Auto-Park" feature from engaging automatically. This may result in a vehicle rollaway. A vehicle rollaway increases the risk of a crash or injury.
NHTSA 26V481000
Vehicle High
Jul 24, 2026 Recall: Jul 24, 2026
Details
Rear Spring Hanger May Detach
ARBOC Specialty Vehicles, LLC (ARBOC) is recalling certain 2017-2026 Spirit of Independence transit buses. The wrong size washers may have been installed on the rear spring hanger bolts. The rear spring hanger may detach from the frame, increasing the risk of a crash.
NHTSA 26V479000
Vehicle High
Jul 24, 2026 Recall: Jul 24, 2026
Details
Maple Leaf Foods Inc. Recalls Not Ready-To-Eat (NRTE) Bacon Product Imported without the Benefit of Import Reinspection
WASHINGTON, JULY 24, 2026 - Maple Leaf Foods, Inc., located in Lisle, Illinois, is recalling approximately 12,036 pounds of not ready-to-eat (NRTE) smoked bacon product that was imported from Canada without the benefit of import reinspection into the United States, the U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) announced today. The NRTE refrigerated smoked bacon product was produced June 9, 2026, June 10, 2026, June 12, 2026, June 13, 2026, and June 15, 2026. The following products are subject to recall [ view labels ]: 12-oz vacuum package of "Royale Natural Applewood Smoked ALL NATURAL Uncured Bacon Product of Canada" with sell by dates of "SEP 01 2026" and "SEP 07 2026" printed on the side of the package 12-oz vacuum package of "TOP VALU Uncured Hardwood Smoked Bacon PRODUCT OF CANADA" with various sell by dates of "SEP 01 2026", "SEP 02 2026", "SEP 04 2026", "SEP 05 2026", and "SEP 07 2026" printed on the side of the package The product subject to recall bears Canadian establishment number "EST. 1" printed on the side the package, and health certificate "2026-S732971612" on master case boxes. This item was further distributed to Grocery Outlet distributors and retailers in Idaho, Oregon, and Washington. The problem was discovered during routine FSIS inspection activities. There have been no confirmed reports of illness or injury due to consumption of these products. Anyone concerned about an illness or injury should contact a healthcare provider. FSIS is concerned that some product may be in consumers' refrigerators and freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase. FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls . Media and consumers with questions regarding the public health alert can contact Adam Emery, Vice President, Communications, Maple Leaf Foods, Inc., at 416-518-5131 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/ .
FSIS 011-2026
Food High
Jul 24, 2026 Recall: Jul 24, 2026
Details
Sviyatp Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violate Virginia Graeme Baker Pool & Spa Safety Act
Sviyatp Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violate Virginia Graeme Baker Pool & Spa Safety Act
This recall involves the Sviyatp white pool drain cover, sold as a replacement pool drain cover for swimming pools. The Sviyatp Pool Drain Cover has no labeling or product identification on the product itself. The pool drain cover comes in clear packaging with "X0050114ZZ," "SV-SP1030-001," "Sviyatp Dual Suction Outlet," and "MADE IN CHINA" printed on the label. The pool drain cover included two stainless steel screws.
CPSC 10877
Consumer Product High
Jul 24, 2026 Recall: Jul 23, 2026
Details
Peony Design Recalls Personalized Baby Bibs and Stroller Bags Due to Risk of Serious Injury or Death from Choking Hazard
Peony Design Recalls Personalized Baby Bibs and Stroller Bags Due to Risk of Serious Injury or Death from Choking Hazard
This recall involves Peony Design personalized handmade baby bibs and stroller bags. The bibs have scalloped edges, a snap closure, and personalized embroidery on the front. The bibs were sold in fabric designs of geese, strawberries, heart tulip, plaid checks, and floral print. The stroller bags were made in coordinating fabrics including heart tulip, plaid check, floral print, and Winnie the Pooh. Each stroller bag has two straps with snaps at the ends for attachment and is personalized with embroidery and a ruffle around the top edge.
CPSC 10880
Child/Baby High
Jul 24, 2026 Recall: Jul 23, 2026
Details
OeyUoc Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violate Virginia Graeme Baker Pool & Spa Safety Act; Sold Exclusively on Amazon by Yuanxinxiang
OeyUoc Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violate Virginia Graeme Baker Pool & Spa Safety Act; Sold Exclusively on Amazon by Yuanxinxiang
This recall involves the OeyUoc white pool drain cover, sold as a replacement pool drain cover for swimming pools. The OeyUoc Pool Drain Cover has no labeling or product identification on the product itself. The pool cover comes in a clear packaging with "X00501CQ7P," "OY-WG1048E-1P," "OeyUoc WG1048…Skimmer Lid SP1030" and "MADE IN CHINA" printed on the label. The pool cover included two stainless steel screws.
CPSC 10878
Consumer Product High
Jul 24, 2026 Recall: Jul 23, 2026
Details
Showing 1,426 - 1,450 of 4,622 product recalls

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