Search by meaning, not just keywords: describe the product or the hazard and we find matching recalls even when the official notice uses different words. Brand names and model numbers work too.
Latest recalls
35,025 found- Lower riskMedical device
Medtronic Neurosurgery recalls Ventriculostomy Kit, REF: 46154
Medtronic Neurosurgery recalls Ventriculostomy Kit REF 461: endotoxin levels may exceed safe limits for cerebrospinal fluid contact, causing inflammation. Affected units sold with UDI-DI 00673978947396 and Lot 2025-08779.
Medtr: NeurosurgeryJun 17, 2026 - Lower riskDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Perampanel CIII Tablets, 6mg, Rx only, 30 Tablets, Mfd.by: Taro Pharmaceutical Industries Ltd., Haifa Bay, Israel
Sun Pharmaceutical recalls Perampanel CIII 6mg tablets due to label mix-up with 10mg tablets. Affected units contain incorrect labeling that may lead to incorrect dosing.
Sun PharmaceuticalJun 17, 2026 - Lower riskMedical device
BD SWITZERLAND SARL recalls 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 MaxPlus Ext Set w/Needleless and Y-Site
BD recalls 60-inch non-DEHP minibore extension sets with UDI-DI codes 10885403236235, 10885403274619, and 10885403237218 due to potential inadequate sterilization processing.
BDJun 16, 2026 - Lower riskMedical device
Copan WASP recalls Brand Name: WASPLab Product Name: WASPLab Model/Catalog Number: W087 Software Version: WebApp version 2.33.1, 2.33.3
WASPLab W087 devices with WebApp versions 2.33.1, 2.33.3, and 2.34.2 may prevent overwriting results. Consumers should check their software version and contact support for updates.
WASPLabJun 16, 2026 - Lower riskMedical device
Olympus Corporation of the Americas recalls Olympus High Flow Insufflation Unit - UHI-4. Model Number: UHI-4
Olympus recalls UHI-4 High Flow Insufflation Units due to potential unexpected display shutdowns causing air delivery to stop. Affected units have specific serial numbers and model numbers.
OlympusJun 16, 2026 - Use cautionMedical device
Medtronic MiniMed, Inc. recalls MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)
Medtronic MiniMed recalls Go app versions 1.0.0 and 1.1.0 for iOS and Android devices. These versions may not trigger nighttime alerts when certain settings are disabled, risking missed insulin doses and hyperglycemia.
Medtronic MiniMedJun 16, 2026 - Use cautionMedical device
Accuray Incorporated recalls Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer; Linear Accelerator
Accuray recalls Cyberknife treatment systems with specific software versions due to risk of collimator falling during treatment. Affected units may require repair or replacement to prevent injury.
AccurayJun 16, 2026 - Use cautionMedical device
Accuray Incorporated recalls Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer; Linear Accelerator
Accuray recalls Cyberknife systems with specific software versions where a collimator could fall during treatment, posing a risk of injury. Affected units include those with Xchange Robotic Collimator Changer and Linear Accelerator running software 11.X or higher.
AccurayJun 16, 2026 - Lower riskDrug
The Harvard Drug Group LLC recalls Carton Label: MAJOR, Methylergonovine Maleate Tablets, USP, 0.2 mg, 20 TABLETS (2 x 10), Rx only, Packaged and
Harvard Drug Group recalls methylergonovine maleate tablets (0.2 mg) with subpotent drug risk. Affected lots expire 09/2026 to 08/2027. Consumers should contact the manufacturer for details.
The Harvard Drug GroupJun 16, 2026 - Use cautionMedical device
Intersurgical Inc recalls One-Piece Guedel Airway, size 00, ISO 5.0, Blue. Oropharyngeal Airway Device.
Intersurgical recalls blue size 00 Guedel airway devices (ISO 5.0) due to potential occlusion. Affected units include specific lot numbers and serial codes. Consumers should contact for details.
IntersurgicalJun 15, 2026 - Lower riskMedical device
Terumo Medical Corporation recalls GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box. Product Code: 60-1060. The Glidesheath Slender is used to
Terumo recalls 5 units per box of Glidesheath Slender A-Kit 6F 10CM (Product Code 60-1060) due to incorrect 0.025 guidewire packaging. This may cause catheter placement issues during medical procedures.
TerumoJun 15, 2026 - Lower riskMedical device
TISSIUM SA recalls Brand Name: COAPTIUM Connect Product Name: COAPTIUM Connect Model/Catalog Number: NCOCO1510 Software Version: N/A
COAPTIUM Connect devices with model NCOCO1510 have a revised shelf life from 36 to 26 months to prevent perioperative breakage during surgery.
COAPTIUM ConnectJun 15, 2026 - Use cautionMedical device
Argon Medical Devices, Inc recalls L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga (1.9F) 0.60mm x 30cm, REF: 384539; 18ga (3.5F) 1.15mm x
Argon Medical recalls specific PICC catheter models due to potential leaking or cracking at the hub, which may cause blood loss, infection, or therapy interruption. Affected units include 26ga and 18ga sizes with certain reference numbers.
Argon MedicalJun 15, 2026 - Use cautionVehicle
FOREST RIVER XLR TOYHAULER (2024) recall — Equipment
Forest River recalls 2023-2024 XLR Toy Haulers with incorrect Gross Vehicle Weight Rating (GVWR) that could lead to overloading and crash risk. Owners must contact customer service for free label correction.
Forest RiverJun 15, 2026 - Stop using nowFood
Western Mixers Produce & Nuts, Inc. recalls FIRST STREET Dark Chocolate Raisins Net Wt. 9 oz. (255g) UPC 797565011830 INGREDIENTS: DARK CHOCOLATE (SUGAR, CHOCOLATE
Western Mixers recalls First Street Dark Chocolate Raisins due to undeclared peanuts. Check your UPC and lot number immediately.
First StreetJun 15, 2026 - Lower riskFood
Vintage Roots LLC recalls Vintage Roots Root Beer Syrup, packaged in glass bottle. Net Wt. 8oz. (236.6 mL). Distributed by Vintage Roots, PO Box
Vintage Roots recalls 8oz root beer syrup containing unapproved sassafras bark. This additive poses health risks and may cause adverse effects. Consumers should check labels for lot code 051626-1 and contact Vintage Roots for details.
Vintage RootsJun 13, 2026 - Use cautionVehicle
LAND ROVER DEFENDER (2026) recall — Air Bags
Land Rover is recalling 2026 Defender vehicles due to driver air bag corrosion risk. Air bags may not deploy in crashes, increasing injury risk. Owners should contact customer service for free lubricant application.
Land RoverJun 13, 2026 - Stop using nowFood
NARA ORGANICS INC recalls a.) nara organics brand; Whole Milk Organic Infant Formula; Milk-based Powder with Iron; 0-12 months; NET WT 24.7 OZ
Nara Organics recalls organic infant formula (0-12 months) due to potential Clostridium botulinum contamination. Consumers should check UPCs and use-by dates for affected lots.
Nara OrganicsJun 13, 2026 - Use cautionMedical device
Sarnova HC, Llc recalls Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack (10 pk), Item Number 670272-KIT
Sarnova HC recalls 2,500 Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipacks (10 pk) with pediatric nasal cannulas instead of adult ones. Affected kits were sold nationwide in 2026.
Sarnova HCJun 12, 2026 - Use cautionVehicle
THOMAS BUILT BUSES SAF-T-LINER HDX2 (2027) recall — Structure
DTNA recalls 2027 Thomas Built SAF-T-LINER HDX2 school buses due to insufficient joint strength. Dealers will add fasteners free of charge starting August 2026.
Thomas Built BusesJun 12, 2026 - Stop using nowVehicle
ALTEC AT SERIES (2025) recall — Power Train
Altec recalls 2014-2026 AT Series aerial devices due to a missing transmission park interlock that may allow operation while not in park.
AltecJun 12, 2026 - Use cautionVehicle
WINNEBAGO REVEL (2026) recall — Equipment
Winnebago is recalling 2026-2027 Revel RVs with incorrect tire labels that could lead to unsafe tire installations and crashes. Owners must contact Winnebago customer service for free label updates.
WinnebagoJun 12, 2026 - Lower riskMedical device
Medline Industries, LP recalls Medline Convenience Kits: 1) LABOR CDS, Model Number: CDS981762B; 2) VAG DELIVERY ADMISSION BAG, Model Number: DYKA1054F
Medline recalls two types of convenience kits due to potential sterility breaches in packaging. If the sterile barrier is compromised, users may face infection risks. Affected kits have specific model numbers and lot numbers.
MedlineJun 12, 2026 - Lower riskMedical device
Tosoh Bioscience Inc recalls ST AIA-Pack Testosterone, IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of testosterone in human serum
Tosoh recalls specific testosterone test kits that may give false high or low results, causing unnecessary treatments or delayed diagnoses. Affected units include certain lot numbers on specific analyzers.
TosohJun 12, 2026 - UnratedDrug
Par Health USA, LLC recalls Buprenorphine HCl, CIII, Injection, 0.3 mg/mL, 5 x 1 mL Single Dose Vials per Carton, Rx Only, For Intramuscular or
Par Health USA recalls specific buprenorphine injections due to crystallization risk. This may affect patients using these medications. Contact your healthcare provider for guidance.
Par HealthJun 12, 2026 - Lower riskDrug
Boehringer Ingelheim Pharmaceuticals, Inc. recalls Synjardy XR Tablets (empagliflozin and metformin hydrochloride extended-release tablets), 12.5/1000 mg, 60 Tablets per
Boehringer Ingelheim recalls Synjardy XR tablets due to potential contamination from incorrect detergent use during production. Affected lots may have unsafe levels of impurities.
Boehringer IngelheimJun 12, 2026 - Lower riskFood
Adams Extract & Spice LLC recalls Smoked Sausage Spice 32.86#
Adams Extract & Spice LLC recalls Smoked Sausage Spice (32.86#) due to undeclared sesame allergen. Affected lots manufactured April 2026. Consumers should avoid use if allergic to sesame.
Adams Extract & SpiceJun 12, 2026 - Stop using nowVehicle
ALTEC AC SERIES CRANE (2025) recall — Equipment
Altec recalls 2024-2026 AC Series Cranes due to missing welds on the IJ26 jib that can cause platform failure. Check your equipment now.
AltecJun 11, 2026 - Use cautionVehicle
INTERNATIONAL HV (2026) recall — Service Brakes, Air
International is recalling certain 2026-2027 HV vehicles due to a potential brake release delay that could increase crash risk. Owners must have the air line replaced by dealers at no cost.
InternationalJun 11, 2026 - Use cautionMedical device
Oxos Medical Inc recalls Brand Name: OXOS Medical, Inc Product Name: MC2 Portable X-Ray System Model/Catalog Number: MC2, MC2.1 Software
OXOS Medical recalls MC2 Portable X-Ray System models MC2 and MC2.1 with software version 5.7.0 due to a defective circuit board that overheats. Affected units have specific serial numbers and UDI codes listed in the recall notice.
OXOS MedicalJun 11, 2026
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