Product recalls today
8 recalls published in the last 7 days. Food, medicines, medical devices, meat and poultry, consumer products and vehicles – 547 recalls since Aug 17, 2026, each with the lot codes, dates and model numbers exactly as the agency lists them.
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Latest recalls
| Date | Recall | Problem | Agency |
|---|---|---|---|
| Oct 15, 2026 |  3M recall: Scotch™ Thermal LaminatorsConsumer products · About 53,634 units | a fire hazard Serious | CPSC |
| Oct 15, 2026 |  usOpal recall: Xalirium Adult Portable Bed RailsConsumer products · About 200 units | an entrapment hazard Lower risk | CPSC |
| Oct 15, 2026 |  Primark recall: 101 Dalmatians Faux Leather Coin PursesConsumer products · About 2,100 units | The coin purses contain higher phthalate concentration levels. Phthalates can be harmful i… Lower risk | CPSC |
| Oct 15, 2026 |  Papablic recall: Bedside Sleepers with Play Yard ExtensionsConsumer products · About 248 units | an entrapment hazard Lower risk | CPSC |
| Oct 15, 2026 |  Loving Thyself Rocks recall: Crystal Glass Cups with Loose Crystal ChipsConsumer products · About 600 units | a laceration hazard Lower risk | CPSC |
| Oct 15, 2026 |  HatsanUSA recall: Blitz and Blitz 777 air riflesConsumer products · About 16,170 units | a projectile hazard Lower risk | CPSC |
| Oct 9, 2026 |  Lippert recall: Seating Power Cord – electrical systemVehicles · 4,435 units (potentially affected) | a fire risk Lower risk | NHTSA Equipment |
| Oct 9, 2026 | Grand Design recall: 2026–2027 Imagine – equipmentVehicles · 148 vehicles (potentially affected) | a crash risk Lower risk | NHTSA Vehicle |
| Oct 8, 2026 | Genesis recall: 2017–2020 G80 and 1 more – seatsVehicles · 94,622 vehicles (potentially affected) | a fire risk Most serious | NHTSA Vehicle |
| Oct 8, 2026 |  Pacearth Direct recall: PACEARTH Swing SeatsConsumer products · About 110,550 units | a fall hazard Serious | CPSC |
| Oct 8, 2026 |  DR Power Equipment recall: Pilot and Premier Trimmer MowersConsumer products · About 42,860 (In addition, about 340 were sold in Canada) | a fire hazard Serious | CPSC |
| Oct 8, 2026 | Honda recall: 2023–2026 Accord Hybrid and 2 more – tiresVehicles · 4,804 vehicles (potentially affected) | an injury risk Lower risk | NHTSA Vehicle |
| Oct 8, 2026 | Tiffin recall: 2022–2025 Allegro Bus and 1 more – fuel systemVehicles · 177 vehicles (potentially affected) | a fire risk Lower risk | NHTSA Vehicle |
| Oct 8, 2026 |  Conqueror recall: Avengers Infinity Gauntlet MedalsConsumer products · About 476 units | a poisoning hazard Lower risk | CPSC |
| Oct 8, 2026 |  Snow Peak recall: Takibi Fireplace Propane Inserts and Lava RocksConsumer products · About 100 units | a fire hazard Lower risk | CPSC |
| Oct 8, 2026 |  Romorgniz recall: Six-Drawer DressersConsumer products · About 12,078 units | an entrapment hazard Lower risk | CPSC |
| Oct 8, 2026 |  Onthewei recall: Baby Bath SeatsConsumer products · About 2,140 units | a tip-over hazard Lower risk | CPSC |
| Oct 8, 2026 |  Giant Bicycle recall: LED-light bike lock keysConsumer products · About 3,630 (In addition, 1,395 in Canada) | a fire hazard Lower risk | CPSC |
| Oct 8, 2026 |  Decathlon recall: Van Rysel GRVL AF BicyclesConsumer products · About 1,150 units | an increased risk of a crash Lower risk | CPSC |
| Oct 7, 2026 |  Draeger recall: VentStar Resus NeoMedical devices · 1,063,643 units | Potential cracks in the hose, which could lead to leakage or the hose falling off. Most serious | FDA Class I |
| Oct 7, 2026 | Medline Industries recall: Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories and 1 more productMedical devices · 771,127 total | a fire hazard Most serious | FDA Class I |
| Oct 7, 2026 |  Salata Dressings recall: Salata Salad Kitchen Jalapen¿o Avocado DressingFood · 1,724 cases | possible Salmonella contamination Most serious | FDA Class I |
| Oct 7, 2026 | Coco G's Snack Foods recall: Coco G's Courmet Flaming Cheddar HotsFood · 270 bags | possible Salmonella contamination Most serious | FDA Class I |
| Oct 7, 2026 | Todd's Seeds recall: Alfalfa Sprouting Seeds and 5 more productsFood · 37,481 retail units (TOTAL) | possible Salmonella and E. coli contamination Most serious | FDA Class I |
| Oct 7, 2026 | Toyota recall: 2026 RAV4 Plug-in Hybrid – engine and engine coolingVehicles · 30,978 vehicles (potentially affected) | a crash risk Serious | NHTSA Vehicle |
| Oct 7, 2026 | Karl Storz Endoscopy recall: HOPKINS Telescope 30¿Medical devices · 6 eyepieces | Due to incorrect inside packaging label for eyepiece. Serious | FDA Class II |
| Oct 7, 2026 | Noxbox recall: NOxBOXi Nitric Oxide Delivery SystemMedical devices · 1,667 units | Potential for irregular oxygen readings due to a manufacturing issue affecting certain oxy… Serious | FDA Class II |
| Oct 7, 2026 | Siemens Healthcare Diagnostics recall: Atellica CH Revised C-Reactive ProteinMedical devices · 42940 units (3938 US, 39002 OUS) | The potential for falsely elevated results. Serious | FDA Class II |
| Oct 7, 2026 | Tandem Diabetes Care recall: T:slim Mobile ApplicationMedical devices · 177 | A beta (early-release) version of the iOS application, version 2.13 (TestFlight) had a sof… Serious | FDA Class II |
| Oct 7, 2026 | Beckman Coulter Mishima K.K recall: Systems/units containing affected software/SQL BECKMAN COULTER CHEMISTRY ANALYZER AU480…Medical devices · 492 units | Certain AU480 chemistry analyzers, with Windows 10 IoT Enterprise 2021 LTSC PCs, may outpu… Serious | FDA Class II |
| Oct 7, 2026 | Olympus Corporation of the Americas recall: Olympus Tripp-Lite P580-025 25ft DisplayPort CableMedical devices · 543 cables | While in the high-power operating mode, a video dropout/blackout may occur when using a pa… Serious | FDA Class II |
| Oct 7, 2026 | Wright Medical Technology recall: CHARLOTTE CLAW ScrewMedical devices · 34 | Screws, intended for use with polyaxial compression plating system intended for foot osteo… Serious | FDA Class II |
| Oct 7, 2026 | Heraeus Medical recall: PALACOS R pro 40 and 3 more productsMedical devices · 33,727 units; 59,660 units; 20,523 units | Potential for monomer liquid leakage. Serious | FDA Class II |
| Oct 7, 2026 | Bard Peripheral Vascular recall: EnCor EnCompass Breast Biopsy and Tissue Removal System ConsoleMedical devices · 99 | Breast biopsy and tissue removal system may experience the following errors: 1) Probe cali… Serious | FDA Class II |
| Oct 7, 2026 | Micro Therapeutics recall: Pipeline Flex Embolization Device with Shield Technology REF PED2-300-12 UDI-DI code…Medical devices · 2 | a labeling error Serious | FDA Class II |
| Oct 7, 2026 | Olympus Corporation of the Americas recall: Olympus M3 Gold Autoclavable Foroblique Telescope 30 and 1 more productMedical devices · 72 units; 50 units | There are identified discrepancies between the sterilization parameters listed in the Inst… Serious | FDA Class II |
| Oct 7, 2026 | Illumina recall: NovaSeq 6000Dx including DRAGEN ServerMedical devices · 80 | Retrospectively reported correction for an instrument intended for targeted sequencing of … Serious | FDA Class II |
| Oct 7, 2026 | Alere San Diego recall: McKesson CONSULT hCG Urine Cassette and 3 more productsMedical devices · 50,265,835; 5,331,585; 13,256,075; 18,139,960 | hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may… Serious | FDA Class II |
| Oct 7, 2026 | Philips recall: Medical Systems Technologies LtdMedical devices · 62 | an increased risk of a crash Serious | FDA Class II |
| Oct 7, 2026 | Penumbra recall: SystemMedical devices · 43 | Due to manufacturing issues reperfusion catheters may fracture. Serious | FDA Class II |
| Oct 7, 2026 | American Nitrile Operations recall: Performance Pro and 2 more productsMedical devices · 99,724,000; 36,793,000; 17,481,000 | Gloves may exhibit defects such as tears, missing fingers, and debris. Use of defective gl… Serious | FDA Class II |
| Oct 7, 2026 | Custom Interventional Pain Management recall: Mastisol Skin AdhesiveMedical devices · 56 | Due to manufacturing issues with the liquid skin adhesive containing in surgical convenien… Serious | FDA Class II |
| Oct 7, 2026 | Volcano recall: Philips IntraSight Plus REF: 797423 and 797417 100-120v-220-240vMedical devices · 19 systems | Software system may associate image data from one patient with another patient's record, p… Serious | FDA Class II |
| Oct 7, 2026 | American Contract Systems recall: Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary…Medical devices · 1,804 kits total | Kits contain manufacturer-recalled perineal care (pericare) wipes within urinary catheter … Serious | FDA Class II |
| Oct 7, 2026 | Cardinal Health 200 recall: Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KITMedical devices · 3677 kits; 344 kits; 2957 kits; 22 kits | a fall hazard Serious | FDA Class II |
| Oct 7, 2026 | Percussionaire recall: Intrapulmonary Percussive Ventilation and 3 more productsMedical devices · 61,858; 98,434; 229,105; 229,430; 228,277; 228,596; 419 | Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunc… Serious | FDA Class II |
| Oct 7, 2026 | Shanghai United Imaging Healthcare recall: Computed Tomography X-ray System and 1 more productMedical devices · 4; 23; 1; 14; 11; 53; 34; 7; 3; 6 | Positron emission tomography and computed tomography x-ray systems have a software problem… Serious | FDA Class II |
| Oct 7, 2026 | Merit Medical Systems recall: Embosphere 500-700 micrometerMedical devices · 104 | Microspheres used in embolization of tumors, prostatic arteries, arteriovenous malformatio… Serious | FDA Class II |
| Oct 7, 2026 | Spectrum Medical SRL recall: Quantum PureFlow Standard Heat Exchanger High Flow 3/8 W and 1 more productMedical devices · 9448; 3232 | Due to blood-to-glycol leak in the heat exchanger. Serious | FDA Class II |
| Oct 7, 2026 | Philips recall: Ingenia Blue Seal SE and Blue Seal XE and 11 more productsMedical devices · 6; 216; 243; 422; 340; 131; 107; 200; 5; 1; 30; 91 | When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR… Serious | FDA Class II |
Recalls by brand
How to read a recall
Identifiers decide whether your product is included. A recall almost never covers every package with a brand name: it lists lot codes, UPC barcodes, best-by or use-by dates, establishment numbers (the “EST.” number inside the USDA mark on meat and poultry), model numbers or – for vehicles – model years and build dates. Compare them with what you have before you throw anything away.
Which agency: the FDA covers most food, medicines, supplements, cosmetics and medical devices; USDA's Food Safety and Inspection Service covers meat, poultry and processed egg products; the CPSC covers consumer products from toys to appliances; NHTSA covers vehicles, tires, child car seats and motor-vehicle equipment. FDA enforcement reports appear weekly and can list a recall several weeks after the company first announced it.
Recall questions
What products were recalled this week?
8 recalls were published by the FDA, USDA, CPSC and NHTSA in the last 7 days, 0 of them in the most serious category: 6 consumer products, 2 vehicles. The newest: 3M recall: Scotch™ Thermal Laminators (Oct 15, 2026).
How do I know if a product I bought is recalled?
Search this page by brand or product name, then compare the lot code, UPC, best-by date or model number on your package with the identifiers on the recall page – a recall usually covers only certain lots or dates, not every product with that name. For a car, enter your 17-character VIN at nhtsa.gov/recalls.
What does Class I recall mean?
The FDA and USDA rate recalls by risk. Class I is the most serious: a reasonable probability that the product will cause serious health problems or death. Class II may cause temporary or reversible health problems; Class III is unlikely to cause harm.
Do I get my money back for a recalled product?
Usually yes. Food recalls ask you to throw the product away or return it to the store for a refund; CPSC recalls offer a free refund, repair or replacement; vehicle safety recalls are repaired free at a dealer. Each recall page shows the remedy the agency lists.
Recalls by type
Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.