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 |
|---|---|---|---|---|---|
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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.
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FDA
Z-2759-2026
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Medical Device | High |
Jul 29, 2026
Recall: Jun 24, 2026
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Details |
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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.
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FDA
Z-2765-2026
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Medical Device | High |
Jul 29, 2026
Recall: Jun 8, 2026
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Details |
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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.
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FDA
Z-2750-2026
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Medical Device | High |
Jul 29, 2026
Recall: Jun 11, 2026
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Details |
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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.
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FDA
Z-2778-2026
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Medical Device | High |
Jul 29, 2026
Recall: Jun 16, 2026
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Details |
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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.
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FDA
Z-2793-2026
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Medical Device | High |
Jul 29, 2026
Recall: May 13, 2026
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Details |
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Penumbra System RED 68 Reperfusion Catheter REF: RED68KIT
Due to manufacturing issues, reperfusion catheters may fractures
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FDA
Z-2770-2026
|
Medical Device | High |
Jul 29, 2026
Recall: Jun 3, 2026
|
Details |
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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.
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FDA
Z-2772-2026
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Medical Device | High |
Jul 29, 2026
Recall: May 19, 2026
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Details |
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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.
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FDA
Z-2753-2026
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Medical Device | High |
Jul 29, 2026
Recall: Jun 11, 2026
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Details |
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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.
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FDA
Z-2755-2026
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Medical Device | High |
Jul 29, 2026
Recall: Jun 11, 2026
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Details |
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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.
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NHTSA
26E050000
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Vehicle | High |
Jul 29, 2026
Recall: Jul 29, 2026
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Details |
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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.
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NHTSA
26E051000
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Vehicle | High |
Jul 29, 2026
Recall: Jul 29, 2026
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Details |
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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.
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NHTSA
26V488000
|
Vehicle | High |
Jul 28, 2026
Recall: Jul 28, 2026
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Details |
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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.
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NHTSA
26V491000
|
Vehicle | High |
Jul 28, 2026
Recall: Jul 28, 2026
|
Details |
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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.
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NHTSA
26V487000
|
Vehicle | High |
Jul 28, 2026
Recall: Jul 28, 2026
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Details |
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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.
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NHTSA
26V489000
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Vehicle | High |
Jul 28, 2026
Recall: Jul 28, 2026
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Details |
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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.
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NHTSA
26V485000
|
Vehicle | High |
Jul 27, 2026
Recall: Jul 27, 2026
|
Details |
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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.
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NHTSA
26V484000
|
Vehicle | High |
Jul 27, 2026
Recall: Jul 27, 2026
|
Details |
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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.
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NHTSA
26V486000
|
Vehicle | High |
Jul 27, 2026
Recall: Jul 27, 2026
|
Details |
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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.
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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.
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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.
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NHTSA
26V479000
|
Vehicle | High |
Jul 24, 2026
Recall: Jul 24, 2026
|
Details |
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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/ .
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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
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.
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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
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.
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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
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.
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CPSC
10878
|
Consumer Product | High |
Jul 24, 2026
Recall: Jul 23, 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.
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