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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UROLOGY MAJOR; Model/Item Number (Kit): WRNM058-10;
Product may be potentially contaminated with a lubricant used during the manufacturing process.
|
FDA
Z-0103-2027
|
Medical Device | High |
Oct 14, 2026
Recall: Aug 10, 2026
|
Details |
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HexaVue Focus Integration System, a single, all-in-one system that handles operating room video routing, surgical video integration, and environmental control, Software Version: 2.0.18
A software issue may result in unintended mismatch of patient information on manually printed images. Incorrect patient information appearing on printed images could create a documentation discrepancy or incorrect association of clinical images with a patient record.
|
FDA
Z-0118-2027
|
Medical Device | High |
Oct 14, 2026
Recall: Sep 23, 2026
|
Details |
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CRANIOTOMY PACK; Model/Item Number (Kit): WRNM035-20;
Product may be potentially contaminated with a lubricant used during the manufacturing process.
|
FDA
Z-0096-2027
|
Medical Device | High |
Oct 14, 2026
Recall: Aug 10, 2026
|
Details |
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Onkos Surgical Inc. My3D Personalized Pelvic Implant, Porous, Left REF PV-ACREC-04M
Personalized pelvic implants inadvertently mixed up and distributed to incorrect customers.
|
FDA
Z-0090-2027
|
Medical Device | High |
Oct 14, 2026
Recall: Jul 24, 2026
|
Details |
|
ADULT HEART TRAY SHANDS JACKS; Model/Item Number (Kit): SHND419-08;
Product may be potentially contaminated with a lubricant used during the manufacturing process.
|
FDA
Z-0094-2027
|
Medical Device | High |
Oct 14, 2026
Recall: Aug 10, 2026
|
Details |
|
VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB007
Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization cycles, the potential hazard is that the biological indicator will show no growth, indicating that the steam cycle was effective, even if the steam cycle did not achieve the intended spore reduction
|
FDA
Z-0071-2027
|
Medical Device | High |
Oct 14, 2026
Recall: Aug 31, 2026
|
Details |
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ROBOTIC PROSTATECTOMY PACK; Model/Item Number (Kit): NAMC423-11;
Product may be potentially contaminated with a lubricant used during the manufacturing process.
|
FDA
Z-0098-2027
|
Medical Device | High |
Oct 14, 2026
Recall: Aug 10, 2026
|
Details |
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VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3060
Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization cycles, the potential hazard is that the biological indicator will show no growth, indicating that the steam cycle was effective, even if the steam cycle did not achieve the intended spore reduction
|
FDA
Z-0072-2027
|
Medical Device | High |
Oct 14, 2026
Recall: Aug 31, 2026
|
Details |
|
Glypto Device, Glypto Cryo Machine;
Lack of 510(k) clearance.
|
FDA
Z-0080-2027
|
Medical Device | High |
Oct 14, 2026
Recall: Aug 24, 2026
|
Details |
|
VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3061
Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization cycles, the potential hazard is that the biological indicator will show no growth, indicating that the steam cycle was effective, even if the steam cycle did not achieve the intended spore reduction
|
FDA
Z-0073-2027
|
Medical Device | High |
Oct 14, 2026
Recall: Aug 31, 2026
|
Details |
|
VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB006
Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization cycles, the potential hazard is that the biological indicator will show no growth, indicating that the steam cycle was effective, even if the steam cycle did not achieve the intended spore reduction
|
FDA
Z-0070-2027
|
Medical Device | High |
Oct 14, 2026
Recall: Aug 31, 2026
|
Details |
|
Battle Bandage, REF: 32-700; Patrol IFAK Bag, Black - Advanced, REF: 81-125-BL; Patrol IFAK Bag, Multicam - Advanced, REF: 81-125-MC; Patrol IFAK II, Olive Drab, Stocked (Option 1), 81-129-OD; IFAK Bag, Intermediate, Black - Stocked, 81-133-BL; IFAK Bag, Intermediate, Coyote Brown - Stocked, 81-133-CB; IFAK Bag, Intermediate, Multicam - Stocked, 81-133-MC; IFAK Bag, Advanced, Black - Stocked, 81-135-BL; IFAK Bag, Advanced, Multicam - Stocked, 81-135-MC; LEO Patrol Kit, 81-139; IFAK Refill, 81-301; IFAK Resupply, 81-303-01; IFAK Resupply - CS/30, 81-303-30; K9 Trauma Kit, 81-605; Medic Enhancem
Compression bandage may be degraded, which may cause unwanted foreign material to be introduced inside the wound, which may lead to wound exploration and irrigation, formation of scar tissue, and infection.
|
FDA
Z-0081-2027
|
Medical Device | High |
Oct 14, 2026
Recall: Sep 2, 2026
|
Details |
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Product Name: Nihon Kohden CNS-6200 Series Central Nurse Station, Model/Catalog Number: CN-6201 Software Version: software versions: 01-03, 01-04, 01-05, 01-06, 02-10, 02-11, and 02-40 Product Description: The device is intended for use by medical professionals to provide cardiac and vital signs monitoring for multiple patients within a medical facility. The CNS-6200 Series Central Nurse Station will display and record physiological data from up to forty telemetry receiver/transmitters and generates an alarm when a measured parameter falls outside a pre-set limit or when life threatening arrhy
Due to a cybersecurity issue associate with a NULL Pointer Dereferences vulnerabiity. If exploited would potentially cause disruption of the centralized monitoring of multiple beds and the visualization of alarms.
|
FDA
Z-0089-2027
|
Medical Device | High |
Oct 14, 2026
Recall: Sep 8, 2026
|
Details |
|
Onkos Surgical Inc. My3D Personalized Pelvic Implant, Porous, Left REF PV-ACREC-04M
Personalized pelvic implants inadvertently mixed up and distributed to incorrect customers.
|
FDA
Z-0091-2027
|
Medical Device | High |
Oct 14, 2026
Recall: Jul 24, 2026
|
Details |
|
Rollator, Bariatric, Basic Steel, Blue, mechanical walker with four legs and a metal frame intended for medical purposes to provide moderate weight support while walking, Product Number MDS86800XWBS
The front fork stem bolt/wheel assembly may disconnect from the rollator frame tubing. If the front fork stem bolt/wheel assembly disconnects from the rollator frame tubing, the front wheels may become loose or detach from the rollator. If the front wheels become loose or detach during use, there is risk of severe adverse events. The immediate consequences could include falls resulting in head trauma, bone fractures, or other critical injuries.
|
FDA
Z-0087-2027
|
Medical Device | High |
Oct 14, 2026
Recall: Aug 14, 2026
|
Details |
|
Spectral CT and Spectral CT 7500 RT; Software Version Numbers: 5.2.X (U.S.); 5.0.X, 5.2.X, 5.4.X (Outside U.S.); Model Numbers: 1. 728333 (U.S. and Outside U.S.), 2. 728340 (Outside U.S.), 3. 728344 (Outside U.S.), 4. 728345 (Outside U.S.);
Software issues may affect the safety and performance of Spectral CT system(s). The issues may result in image artifacts, wrong slice thickness, or unintended system motion.
|
FDA
Z-0078-2027
|
Medical Device | High |
Oct 14, 2026
Recall: Aug 21, 2026
|
Details |
|
Brand Name: MiniMed Flex Product Name: MiniMed Flex Insulin Pump Model/Catalog Numbers: MMT-8062; MMT-8072 Product Description: The MiniMed Flex pump is an alternate controller enabled (ACE) pump intended for the subcutaneous delivery of insulin, at set and variable rates, for the management of diabetes mellitus in persons requiring insulin. It can reliably and securely communicate with compatible digitally connected devices, including an integrated continuous glucose monitor (iCGM), interoperable Medtronic continuous glucose monitor (CGM), and interoperable automated glycemic controller (iAGC
Some MiniMed Flex insulin pumps were released with missing (i.e., devices with no result or abort test results are presumed to have failed) or failed verification test results in one or more of 9 functional tests. The unverified/failed pumps released to users potentially have one or more of the following issues: inoperable pump at setup, lack of protection for moisture exposure, slow battery charging, disconnection issues with other system components (i.e., continuous glucose monitoring sensor or MiniMed mobile app), reduced ability to detect occlusion events, compromised audio for pump alarms/alerts, and/or inaccurate insulin delivery.
|
FDA
Z-0088-2027
|
Medical Device | High |
Oct 14, 2026
Recall: Aug 20, 2026
|
Details |
|
VERIFY Biological Steam Test Pack Model/Catalog Number: S3065
Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization cycles, the potential hazard is that the biological indicator will show no growth, indicating that the steam cycle was effective, even if the steam cycle did not achieve the intended spore reduction
|
FDA
Z-0074-2027
|
Medical Device | High |
Oct 14, 2026
Recall: Aug 31, 2026
|
Details |
|
BARD EP XT DECAPOLAR STEERABLE, DIAGNOSTIC EP CATHETER, 6F, LARGE 4.0, 10, 2-5-2MM, REF: 201007
Diagnostic electrophysiology (EP) catheter may have a breached sterile barrier on the straight seal side of the primary pouch, which if used could lead to particulate embolization, infection, thrombus or ganuloma formation from particulate matter.
|
FDA
Z-0085-2027
|
Medical Device | High |
Oct 14, 2026
Recall: Aug 18, 2026
|
Details |
|
Missing Circuit Protection on Charge Line
K.Z., Inc. (K.Z.) is recalling certain 2026-2027 SportTrek Fifth Wheel recreational trailers. The charge line may not have circuit protection. An unprotected charge line can cause the wire to overheat, increasing the risk of a fire.
|
NHTSA
26V672000
|
Vehicle | Unknown |
Oct 13, 2026
Recall: Oct 13, 2026
|
Details |
|
Head Restraint Cushion May Detach
Volvo Car USA, LLC (Volvo Car) is recalling certain 2025-2026 EX30 and 2026 EX30CC vehicles. The head restraint cushion may detach during a crash. A detached head restraint cushion can increase the risk of injury during a crash.
|
NHTSA
26V671000
|
Vehicle | High |
Oct 9, 2026
Recall: Oct 9, 2026
|
Details |
|
Incorrect Tire Size and Pressure Information on Label/FMVSS 110
Grand Design RV, LLC (Grand Design) is recalling certain 2027 Transcend travel trailers. The tire information label may state the incorrect tire size and cold inflation pressure. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 110, "Tire Selection and Rims." Referencing incorrect information can result in installing the wrong size replacement tires or underinflating the tires, increasing the risk of a crash.
|
NHTSA
26V668000
|
Vehicle | High |
Oct 9, 2026
Recall: Oct 9, 2026
|
Details |
|
Seating Power Cord May Have Inadequate Circuit Protection
Lippert is recalling certain power seating assemblies. The power cord fuse may not provide adequate circuit protection. In the event of a short circuit, inadequate protection increases the risk of a fire.
|
NHTSA
26E070000
|
Vehicle | Unknown |
Oct 9, 2026
Recall: Oct 9, 2026
|
Details |
|
Park Outside: Fire from Overheated Power Seat Motors
Hyundai Motor America (Genesis) is recalling certain 2015-2016 Hyundai Genesis, and 2017-2020 Genesis G80 vehicles. The front power seat motors may overheat due to a stuck power seat control switch, which can result in a fire while parked or driving. A fire increases the risk of injury.
|
NHTSA
26V664000
|
Vehicle | High |
Oct 9, 2026
Recall: Oct 9, 2026
|
Details |
|
Safety Chains Are Underrated For GVWR
Grand Design RV, LLC (Grand Design) is recalling certain 2026-2027 Imagine travel trailers. The installed safety chains are underrated for the Gross Vehicle Weight Rating (GVWR). Underrated chains can allow the trailer to detach from the tow vehicle, increasing the risk of a crash.
|
NHTSA
26V667000
|
Vehicle | High |
Oct 9, 2026
Recall: Oct 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.