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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TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia Tracking Array REF 109004 UDI-DI code: M9461090040 TMINI Miniature Robotic System is indicated as a stereotaxic instrumentation system for total knee replacement (TKA) surgery. It is to assist the surgeon by providing software-defined spatial boundaries for orientation and reference information to identifiable anatomical structures for the accurate placement of knee implant components
Due to manufacturing/design issue where the knob on the tracking array may loosen causing potential misalignment of the array.
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FDA
Z-2716-2026
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Medical Device | High |
Jul 15, 2026
Recall: May 8, 2026
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Details |
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Brand Name: Geneva Product Name: Brachytherapy Applicator Product Description: The device is intended for intracavitary brachytherapy for cancer treatment of the cervix and the endometrium. Optional needles can be placed for interstitial therapy.
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.
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FDA
Z-2712-2026
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Medical Device | High |
Jul 15, 2026
Recall: Apr 3, 2026
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Details |
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Brand Name: Brachytherapy Applicator Product Name: Advanced Gynecological Applicator Product Description: The intended use of the Advanced Gynecological Applicator is intracavitary brachytherapy for cancer treatment of the cervix and endometrium. Optional needles can be placed for interstitial brachytherapy.
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.
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FDA
Z-2711-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Apr 3, 2026
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Details |
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5008X Blood Tubing Set, 24 units per case. Includes the below model numbers and descriptions. 1. 5008X HD Pre-Flush Standard Blood Tubing Set; Model Number: 03-5110-6. 2. 5008X HD Pre-Flush With Twister Blood Tubing Set; Model Number: 03-5160-1. 3. 5008X HD/HDF Standard Blood Tubing Set; Model Number: 03-5300-3. 4. 5008X HD/HDF With CLiC Blood Tubing Set; Model Number: 03-5300-3C. 5. 5008X HD/HDF With Twister Blood Tubing Set; Model Number: 03-5350-8.
Potential for Online Port Errors due to connection issues when connecting the SafeLine of the 5008X CAREset to the substitution fluid port of the 5008X CAREsystem.
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FDA
Z-2702-2026
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Medical Device | High |
Jul 15, 2026
Recall: May 11, 2026
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Details |
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Brand Name: Fletcher CT/MR Shielded Applicator Set Product Name: Intracavitary Remote Afterloading Applicator Product Description: The Fletcher CT/MR Shielded Applicator Set is intended for gynecological brachytherapy treatment of the cervix and endometrium.
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.
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FDA
Z-2710-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Apr 3, 2026
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Details |
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Atellica CH Enzymatic Hemoglobin A1c (A1c_E). Material Number: 11097536.
The potential for intermittent well-to-well bias on the A1c_E assay on the Atellica CH and Atellica CI analyzer which could cause falsely depressed or falsely elevated HbA1c patient results.
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FDA
Z-2703-2026
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Medical Device | High |
Jul 15, 2026
Recall: Jun 8, 2026
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Details |
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Medline Convenience Kits: 1) ANESTHESIA KIT PEDS 90-LF, Model Number: DYNJAP10125A
Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm general purpose temperature probe-size 9 due to an error in its distribution control process.
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FDA
Z-2695-2026
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Medical Device | High |
Jul 15, 2026
Recall: May 28, 2026
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Details |
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Brand Name: Versius Surgical System US Product Name: Vesius Surgeon Console US Model/Catalog Number: V-SS-1020 Software Version: Pratchett 1 version 62.1 Product Description: The Versius Surgical System is a modular, open console, software controlled, electromechanical system designed for surgeons to perform minimally invasive surgery.
Secure Boot was mistakenly not enabled at manufacturing time, which presents a potential cybersecurity risk.
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FDA
Z-2717-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Jun 9, 2026
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Details |
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Olympus Single Use Distal Cover, Catalog Number MAJ-2315, Used with: EVIS EXERA III Duodenovideoscope TJF-Q190V- designed to be attached to Olympus duodenovideoscopes to cover the distal end of the insertion tube and around the forceps elevator; duodenoscope and accessories, flexible/rigid
Olympus has developed and released newly designed version of the Distal Cover (MAJ-2315) to replace previous design of the Single Use Distal Covers.
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FDA
Z-2676-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Jun 5, 2026
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Details |
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MiniMed 780G Insulin Pump, REF: MMT-1885, MMT-1886, MMT-1895, MMT-1896
A software anomaly can occur when the pump is paired with the Instinct sensor. Under certain circumstances, the pump unexpectedly stops delivering insulin and displays two error messages back-to-back: Pump Error 53 followed immediately by Pump Error 23. Insulin delivery will stop which may lead to delayed therapy and an increased risk of hyperglycemia or diabetic ketoacidosis (DKA).
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FDA
Z-2698-2026
|
Medical Device | High |
Jul 15, 2026
Recall: May 27, 2026
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Details |
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KL Owen Custom Orthodontic Solution, model/catalog number CIAS-800033,
A product error defect may cause incorrect bracket placement.
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FDA
Z-2699-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Jun 8, 2026
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Details |
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GSP Neonatal GALT Kit. Product Codes: 3303-001U, 3303-0010. in vitro diagnostic. Used in FLUORESCENT PROC. (QUAL), GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE.
Reduction in the on-board stability of the GSP GALT assay. This may increase the likelihood of run-QC failures and consequently delay the reporting of patient results.
|
FDA
Z-2713-2026
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Medical Device | High |
Jul 15, 2026
Recall: May 18, 2026
|
Details |
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Aquacel Ag Surgical SP REF: 413556 9cm x 15cm/3.5 in. x 6 in., Sterile R
Surgical dressing manufactured out of specification (greater thickness).
|
FDA
Z-2677-2026
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Medical Device | High |
Jul 15, 2026
Recall: Jun 8, 2026
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Details |
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Incorrect GAWR on Certification Label/FMVSS 110
Nissan North America, Inc. (Nissan) is recalling certain 2020-2026 Nissan Armada, 2011-2013 Infiniti QX56, and 2014-2027 QX80 vehicles equipped with 22" wheels. The Gross Axle Weight Rating (GAWR) listed on the certification label is incorrect, which can allow the vehicle to be overloaded. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 110, "Tire Selection and Rims." An overloaded vehicle can increase the risk of a crash.
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NHTSA
26V455000
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Vehicle | High |
Jul 15, 2026
Recall: Jul 15, 2026
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Details |
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Drive Mode May Disengage Causing a Loss of Drive Power
E-One Incorporated (E-One) is recalling certain 2026 Commercial, 2025-2026 Typhoon N, and Cyclone N emergency vehicles. The drive/pump mode transfer case may disengage, causing loss of power to the rear wheels. Loss of power to the rear wheels can prevent the vehicle from moving, increasing the risk of a crash.
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NHTSA
26V454000
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Vehicle | High |
Jul 15, 2026
Recall: Jul 15, 2026
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Details |
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Trailer Brakes and Lighting May Be Lost/FMVSS 108
Ford Motor Company (Ford) is recalling certain ITRM accessory kits with part number RL3Z-19H322-AA, ML3Z-19H322-AA, AB, BA, BB, CA, and CB that were sold as aftermarket accessory kits for Ford 2021-2026 F-150 vehicles. The integrated trailer module (ITRM) may lose communication with the vehicle, causing a loss of brake function, turn signals and brake lights. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 108, " Lamps, Reflective Devices, and Associated Equipment." A loss of trailer brakes or lights can reduce the driver’s ability to control the trailer and decrease the trailers visibility to other road users, increasing the risk of a crash.
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NHTSA
26E046000
|
Vehicle | High |
Jul 14, 2026
Recall: Jul 14, 2026
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Details |
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Second-Row Seat May Move Unexpectedly
Ford Motor Company (Ford) is recalling certain 2020-2027 Aviator and 2020-2026 Explorer vehicles. The switch for the easy-entry second-row outer seats may bind or stick, resulting in the seats unlatching, tipping, or sliding unexpectedly. A seat that moves unexpectedly may not properly restrain an occupant during a crash, increasing the risk of injury.
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NHTSA
26V451000
|
Vehicle | High |
Jul 14, 2026
Recall: Jul 14, 2026
|
Details |
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Roof Rail Covers May Detach
Ford Motor Company (Ford) is recalling certain 2016-2019 Explorer vehicles. The roof rail covers may come loose and detach from the vehicle. A detached roof rail cover can create a road hazard, increasing the risk of a crash.
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NHTSA
26V448000
|
Vehicle | High |
Jul 14, 2026
Recall: Jul 14, 2026
|
Details |
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Seat Belt Buckle May Fail
Hyundai Motor America (Hyundai) is recalling certain 2025 Kona Electric and 2026 Kona vehicles. The seat belt buckle in the rear center seat may fail to properly restrain an occupant during a crash. A seat belt buckle that fails to properly restrain an occupant in a crash increases the risk of injury.
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NHTSA
26V452000
|
Vehicle | High |
Jul 14, 2026
Recall: Jul 14, 2026
|
Details |
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ADS Software May Fail to Detect and Respond to Heavy Smoke
Zoox, Inc. (Zoox) is recalling certain Automated Driving Systems (ADS). The ADS software may fail to detect heavy smoke, allowing the vehicle to enter an area of low visibility, particularly active emergency scenes. Failing to respond to low visibility conditions can increase the risk of a crash or impede first responders.
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NHTSA
26E044000
|
Vehicle | High |
Jul 10, 2026
Recall: Jul 10, 2026
|
Details |
|
Loss of Steering
Tenneco Automotive (DRiV) is recalling certain NAPA steering inner tie rod ends, part number 269-3813 sold as replacement parts for 2013-2018 Ford C-Max, 2013-2019 Escape, and 2012-2018 Focus vehicles. The tie rod end stud may separate, causing a loss of steering. A loss of steering increases the risk of a crash.
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NHTSA
26E045000
|
Vehicle | High |
Jul 10, 2026
Recall: Jul 10, 2026
|
Details |
WonderStone Infant Walkers Recalled Due to Risk of Serious Injury or Death from Fall Hazard; Violate Mandatory Standard for Infant Walkers; Sold on Walmart.com by Wonder Stone Toys
This recall involves WonderStone-branded Infant Walkers sold in green and pink. The walkers have a gray fabric seat, a white tray with a detachable music box, six wheels, a foot pad and a white hand lever. "Model No: 616" or "Model No: 616-1" is printed on a white label located under the tray.
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CPSC
10857
|
Child/Baby | High |
Jul 10, 2026
Recall: Jul 9, 2026
|
Details |
Moodooy Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by Yuezhang
This recall involves the Moodooy-branded adult portable bed rail. The bed rail has a white frame with black trim and a black storage pocket. The brand name "Moodooy" and model "F311" are printed on the storage pocket. The bed rail is about 12 inches wide by about 21 inches tall to about 23 inches tall (when extended).
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CPSC
10856
|
Consumer Product | High |
Jul 10, 2026
Recall: Jul 9, 2026
|
Details |
Flaunt Recalls Magsafe Battery Chargers Due to Risk of Serious Injury or Death from Fire and Burn Hazards
This recall involves the Flaunt MagSafe Battery Charger power banks with model number E33A. "FLAUNT" is engraved on the front right side of the power bank and there is a small circular button in the bottom center of the front side of the power bank. The back label of the unit is marked "FLAUNT" and "Model: E33A". The power banks were sold in melon, black, lavender and white. The chargers measure 3 by 2 by 0.25 inches and weigh around 3.2 ounces.
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CPSC
10858
|
Electronics | High |
Jul 10, 2026
Recall: Jul 9, 2026
|
Details |
Biometric Gun Safes Recalled Due to Serious Injury Hazard and Risk of Death; Sold Exclusively on Amazon.com by BBRKIN
This recall involves BBRKIN and MouTec Biometric Gun Safes with model number QHXP029B. The gray steel safes are used to store firearms and valuables. The safes measure about 14 inches by 12 inches by 57 inches, have one shelf and can store approximately five firearms. The recalled safes have the following serial number range: SQC200034980 - SQC202319171. The serial number is on a label on the lower right corner of the front of the safes. The brand name "MouTec" or "BBRKIN" is on the upper right corner of the front of the safes.
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CPSC
10855
|
Consumer Product | High |
Jul 10, 2026
Recall: Jul 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.
New vehicle, tire, equipment and child-seat campaigns include defect summaries, affected units, remedy notes and NHTSA campaign numbers.
Recent recall pages are date-driven. Use the published date and recall date to understand whether an alert is new, newly classified or recently updated.
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.
The site syncs official recall sources daily and stores updated records by source agency, dataset and official recall ID.
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.
Match the brand, product name, package size, UPC, lot code, best-by date, allergen or contamination issue and distribution area before taking action.
Yes. Use the risk filter or highest-risk sort to surface recalls marked critical or high risk across all official sources.