FDA · USDA · CPSC · NHTSA · updated twice a day
Medical device recalls
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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Consumer products6this week
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Latest recalls
| Date | Recall | Problem | Agency |
|---|---|---|---|
| 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 | 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 |
| Oct 7, 2026 | ASP Global recall: Disposable Tourniquet Cuff and 18 more productsMedical devices · 5015; 18; 400; 3020; 70; 25350; 38380; 4610; 7650; 6100; 15770; 26810; 32390; 2600; 4530; 1220; 260; 10; 156; 240; 1692; 1899; 396; 2112; 27090; 8807; 12114; 5738; 33102; 6319; 2304; 2244; 1056; 36; 10060; 36680; 55050; 15580; 20760; 34550; 45960; 53040; 65640; 4850; 6510; 30; 20; 50; 2750; 1740; 970; 1100; 820; 850; 4480; 410; 360; 40; 80; 100; 180; 5440 | Due to incorrect expiration date on product manufactured between September 2016 to March 2… Serious | FDA Class II |
| Oct 7, 2026 | HeartSine Technologies recall: HeartSine samaritan PADMedical devices · 31,834 | Products were distributed without the required Maintenance Supplement, which describes an … Lower risk | FDA Class III |
| Sep 30, 2026 | Boston Scientific recall: Imager II Angiographic Catheters M001314001 IMAGER II/5/ST/65/038 BX5Medical devices · 262,686 | Tip may fracture or detach, leading to device fragments remaining within the patient or mi… Most serious | FDA Class I |
| Sep 30, 2026 | AVID Medical recall: Halyard IV START KIT NON-STERILEMedical devices · 288 kits (6 cases) | Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may be contaminat… Most serious | FDA Class I |
| Sep 30, 2026 | CooperSurgical recall: INCA (Infant Nasal Cannulae Assy) Infant Nasal CPAP, Complete Set. Stay-Flex tubing… and 1 more productMedical devices · 2,643 boxes (13,215 units); 149 boxes (745 units) | Potential to exhibit a loose connection between the flexible tubing and the nasal cannula,… Most serious | FDA Class I |
| Sep 30, 2026 | Baxter Healthcare recall: Volara, HC, Na aMedical devices · 2 | Contamination within the release test equipment flow path could have affected the accuracy… Serious | FDA Class II |
| Sep 30, 2026 | Becton, Dickinson and recall: ForeSight Elite Tissue Oximetry Cable REF HEMFSM10 UDI-DI code: 00690103210927 The…Medical devices · 15,455 cables | Due to incorrect switching of Channel 1 and 2 on the module and flag labels on the tissue … Serious | FDA Class II |
| Sep 30, 2026 | Seaspine Orthopedics recall: Extended Polyaxial HeadMedical devices · 270 units | The proximal thread depth of the spinal device is out of design specification. Serious | FDA Class II |
| Sep 30, 2026 | Philips Ultrasound recall: Philips EPIQ Elite Diagnostic Ultrasound System Model # 795234Medical devices · 219 units | Due to software issue with ultrasound system, doppler sample is displayed shallower than i… Serious | FDA Class II |
| Sep 30, 2026 | Maquet SAS recall: PowerLED 300 Concealed Lighting SystemMedical devices · 667 | a fall hazard Serious | FDA Class II |
| Sep 30, 2026 | CooperVision recall: (somofilcon A) Contact LensMedical devices · 3060 | A small number of lenses within the affected lot are of the incorrect power. Serious | FDA Class II |
| Sep 30, 2026 | Cardinal Health 200 recall: Presource Convenience Kits: 1) KITMedical devices · 17503 kits; 9480 kits | The kits contain applicators that may exhibit an open or incomplete seal on the packaging … Serious | FDA Class II |
| Sep 30, 2026 | AVID Medical recall: Halyard IV START KIT NON-STERILEMedical devices · 816 kits (17 cases); 192 kits (4 cases) | Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may exhibit an op… Serious | FDA Class II |
| Sep 30, 2026 | Baxter Healthcare recall: Pro+ MRS Surface for Versacare and 2 more productsMedical devices · 169 units; 824 units; 6 units | There is an error in the product description on the Unique Device Identification (UDI) lab… Serious | FDA Class II |
| Sep 30, 2026 | DeRoyal Industries recall: REF: 81-030415 Myocardial Probe Non-PyrogenicMedical devices · 7 cases, 140 units | Myocardial temperature probes contain an incorrect needle. Specifically, an 18mm needle wa… Serious | FDA Class II |
| Sep 30, 2026 | New York Embroidery Studio recall: Trinity Non-Surgical Isolation GownMedical devices · 5,400 gowns | Gowns do not consistently meet the minimum liquid-barrier performance required. Serious | FDA Class II |
| Sep 30, 2026 | Ventec Life Systems recall: HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve and 2 more productsMedical devices · 21 units; 2 units; 25 units | Labeling; Oxygen Cylinders do not contain required medical gas labeling Serious | FDA Class II |
| Sep 30, 2026 | Heidelberg Engineering recall: SPECTRALIS with Flex ModuleMedical devices · 87 | a tip-over hazard Serious | FDA Class II |
| Sep 30, 2026 | Medline Industries recall: Medline Convenience Kits: 1) PEDS SINUS PACK and 4 more productsMedical devices · 695 kits; 128 kits; 486 kits; 234 kits; 4013 kits | The kits contain neurological sponges with the potential for unexpected variability of end… Serious | FDA Class II |
| Sep 30, 2026 | Olympus Corporation of the Americas recall: Olympus EZDilate Endoscopic Balloon Dilator Wired-guided 11Medical devices · 305 units | Potential for the inflation chart label affixed to the shaft of the device to be incorrect… Serious | FDA Class II |
| Sep 30, 2026 | Intervascular, Sas recall: Cardioroot Woven Collagen Coated Vascular GraftMedical devices · 16329 (3880 US, 12449 OUS) | Product failed to meet the specified acceptance criteria for Integral Water Permeability (… Serious | FDA Class II |
| Sep 30, 2026 | Biomerieux recall: Vitek 2 Ast-N461 Test KitMedical devices · 97680 units | The issue is related to card pouch damage associated with a portion of the lot which was p… Serious | FDA Class II |
| Sep 30, 2026 | Criticare Technologies recall: NGenuity Patient Monitor with CapnographyMedical devices · 1,007 | Complaint trend where "Checkline Error" alarm presents at device setup, rendering the CO2 … Serious | FDA Class II |
3 or more recalls
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.
FAQ
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: Draeger recall: VentStar Resus Neo (Oct 7, 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.
More
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.