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- Use cautionVehicle
CHEVROLET SILVERADO 2500 (2019) recall — Air Bags
Chevrolet is recalling 2019 Silverado 2500 vehicles with a risk of air bag end cap detachment causing injury. Owners must contact GM for free replacement of RRAB modules.
ChevroletMay 21, 2026 - Lower riskMedical device
Medical Action Industries, Inc. 306 recalls Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear Sequence Model/Catalog Number: 78791
Recall of Medical Action Industries Dialysis Change Tray Clear Sequence model 78791 due to improper silicone seal that may cause doming or tearing. Affected units sold with specific lot codes.
Medical Action IndustriesMay 21, 2026 - Lower riskMedical device
Instrumentation Laboratory recalls GEM Premier 5000 PAK Part Numbers: 00055360010 00055360011 00055407504 00055415010 00055430010 00055430011 00055445010
Instrumentation Laboratory recalls specific GEM Premier 5000 PAK models due to lysing bag solution concentration issues that may delay detection of blood abnormalities.
Instrumentation LaboratoryMay 21, 2026 - Lower riskFood
Galliker Dairy Co, Inc. recalls DQ Chocolate Reduced Fat Ice Cream Mix, 5 GAL (18.9L). Keep refrigerated.
Galliker Dairy recalls 5-gallon DQ Chocolate Reduced Fat Ice Cream Mix due to metal shavings found in product. Consumers should check for metal shavings before use.
Galliker DairyMay 21, 2026 - Use cautionVehicle
JEEP GRAND WAGONEER (2026) recall — Back Over Prevention
Chrysler recalls 2026 Jeep Grand Wagoneers with rear camera that may not display, risking crashes. Owners must have dealer inspect wiring harness free of charge.
ChryslerMay 21, 2026 - Lower riskMedical device
Karl Storz Endoscopy recalls Flexible Hystero-Fiberscope Kits REF: 11264BBU1, 11264BBUK1, that contain expired Single Use Endoscopic Seal: GYN, REF:
Karl Storz recalls flexible hystero-fiberscope kits with expired single-use endoscopic seals for gynecology procedures, which could compromise sterility during medical use.
Karl StorzMay 21, 2026 - Use cautionVehicle
CHRYSLER PACIFICA (2023) recall — Back Over Prevention
Chrysler is recalling 2023 Pacifica models with rearview camera that may not display, increasing crash risk. Owners must update software or replace module by July 2026.
ChryslerMay 21, 2026 - Use cautionVehicle
JEEP GRAND CHEROKEE L (2025) recall — Air Bags
Chrysler recalls 2022-2026 Jeep Grand Cherokee L vehicles with potential delayed side air bag deployment during crashes, increasing injury risk. Owners must update software via dealer by June 2026.
ChryslerMay 21, 2026 - Use cautionVehicle
ALLIANCE RV VALOR (2025) recall — Equipment
Alliance recalls 2022-2025 Valor RVs with heating pads that may overheat near lithium batteries, risking fire. Owners must have heating pads replaced by dealers.
AllianceMay 21, 2026 - Lower riskMedical device
Laborie Medical Technologies Corp recalls Solar GI System (Water Perfusion); Product Name (Catalog Number): Solar GI LGI H2O, 12p, Trolley system (G3-6), Solar
Laborie Medical recalls Solar GI H2O systems (G3-6 to G3-14) due to moisture accumulation in pneumatic circuits that may affect airflow or pressure measurements.
Laborie MedicalMay 21, 2026 - Use cautionMedical device
BD SWITZERLAND SARL recalls BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382903949106 BD Connecta" Stopcocks are used to administer
BD recalls Luer-Lok 360 stopcocks with UDI-DI code 00382903949106 due to potential overthreading causing unstable connections during IV fluid administration.
BDMay 21, 2026 - Lower riskMedical device
Windstone Medical Packaging, Inc. recalls A M S, ALIGNED MEDICAL SOLUTIONS, Dr. Lewin Pack, Pack Number AMS7200D, surgical convenience kit
Windstone Medical Packaging recalls surgical convenience kits with contaminated alcohol prep pads. The kits contain a contaminant (Paenibacillus phoenicis) found during sterilization audits. Affected kits have specific lot numbers.
Windstone Medical PackagingMay 21, 2026 - Lower riskMedical device
Elekta, Inc. recalls MOSAIQ Oncology Information System
Elekta recalls MOSAIQ Oncology Information System software version 3.2 due to potential failure to load adapted baseline shift plans during treatment, risking incorrect radiation therapy delivery.
ElektaMay 21, 2026 - Use cautionMedical device
Baxter Healthcare Corporation recalls Hillrom VOLARA System P.CIRCUIT KIT AC (Single Patient Use Circuit), Model/Catalog Number REF M08473; Oscillation Lung
Hillrom recalls Volara System circuit kits with potential air leaks causing oxygen drops. Affected units have model REF M08473 and were sold starting April 28, 2025. Stop using if leaks occur.
HillromMay 21, 2026 - Lower riskMedical device
Papablic Inc recalls Papablic Replacement Brush Heads. Model Number: PAPA317AA.
Papablic recalls replacement brush heads (model PAPA317AA) with specific lot numbers and date codes due to potential breakage. Affected customers should check their product details.
PapablicMay 21, 2026 - UnratedMedical device
Medline Industries, LP recalls Medline Convenience Kits: 1) SUTURE TRAY, Model Number: SUT12260; 2) CHEST TUBE INSERTION TRAY, Model Number: MNS3390;
Medline recalls 31 convenience kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules due to quality issues found during FDA inspection.
MedlineMay 21, 2026 - Lower riskMedical device
Boston Scientific Corporation recalls CRE Pro Wireguided 12-15mm 240cm
Boston Scientific recalls CRE Pro Wireguided 12-15mm 240cm catheters due to potential sterile breach in packaging. Affected units have specific lot numbers and expiration dates. Consumers should check their product details and contact the company for guidance.
Boston ScientificMay 21, 2026 - UnratedMedical device
Bard Access Systems, Inc. recalls CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 CK000566 Poly Midline Catheter 4 Fr
Bard recalls specific poly midline catheters due to lidocaine ampoules made under deficient manufacturing practices. Affected units have UDI-DI codes 00801741121609 and 00801741108051. Contact Bard for details.
BardMay 21, 2026 - Lower riskDrug
Keystone Industries recalls DHP Topical Anesthetic Gel, Benzocaine 20%, Strawberry Flavor, 1 oz. (30 g), Manufactured for and Distributed by Dental
Keystone Industries recalls DHP Topical Anesthetic Gel (Benzocaine 20%) due to potential incomplete seals in containers. This may lead to product leakage or contamination. Affected units have NDC 69634-020-30 and expire 04/15/2029.
Keystone IndustriesMay 21, 2026 - Lower riskFood
Fairhope Roasting Company recalls Fairhope Roasting Company Cold Brew Coffee Concentrate, packaged in 1-gallon plastic jugs, UPC 852236006062, for food
Fairhope Roasting Company recalls cold brew coffee concentrate jugs due to missing refrigeration label. This could cause spoilage if stored at room temperature.
Fairhope Roasting CompanyMay 21, 2026 - Use cautionFood
Alb-USA Enterprises Inc recalls El David Gelee, Bonbons with fruits Soft & Juicy, 400g. Packaged in decorated paperboard box and covered entirely in
Alb-USA Enterprises recalls El David Gelee Bonbons due to undeclared FD&C Yellow 5 and Red 40. Check your UPC and expiration date.
El DavidMay 21, 2026 - Stop using nowConsumer product
Resistance Bands Recalled Due to Serious Injury from Impact Hazard; Imported by HomeProGym
HomeProGym's purple 60-pound and gray 70-pound resistance bands can separate during use, risking serious injury. Consumers must stop using these bands immediately and return them for a refund or $50 store credit.
HomeProGymMay 21, 2026 - Stop using nowConsumer product
PandaEar Recalls Portable Hook-On Chairs Due to Risk of Serious Injury or Death from Fall Hazard; Violates Mandatory Standard for Portable Hook-On Chairs
PandaEar recalls two portable hook-on chairs due to crotch restraints that can be removed without tools, causing infants to fall through openings. Consumers must stop using immediately and return for refund.
PandaEarMay 21, 2026 - Stop using nowConsumer product
Orb Funkee Squeeze Toys Recalled Due to Risk of Serious Injury or Death from Asbestos Exposure; Imported by The Orb Factory
Orb Funkee Squeeze Toys with date code 3102491A may contain asbestos in sand. Stop using immediately and contact for refund. Risk of serious injury or death if inhaled.
OrbMay 21, 2026 - Stop using nowConsumer product
Lil Pick Up Recalls Youth All-Terrain Vehicles (ATVs) Due to Risk of Serious Injury or Death from Crash and Burn Hazards; Violates Mandatory Standard for ATVs
Lil Pick Up recalls Sierra 125U youth ATVs due to crash, burn, and suspension hazards. Stop using immediately for a full refund.
Lil Pick UpMay 21, 2026 - Stop using nowConsumer product
Bethlehem Lights Recalls Bethlehem Lights 10-inch Illuminated Ribbon Spheres Due to Risk of Serious Injury or Death from Fire Hazard; Sold by QVC
Bethlehem Lights recalls 10-inch illuminated ribbon spheres sold by QVC due to fire risk. Stop using immediately and request a full refund.
Bethlehem LightsMay 21, 2026 - Stop using nowConsumer product
ABC Trading Recalls WSDZ Light-up Glasses Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Button Cell Batteries
ABC Trading recalls WSDZ Light-up Shot Glasses due to button cell batteries accessible to children, posing ingestion risk. Stop using immediately and dispose safely.
ABC TradingMay 21, 2026 - Stop using nowConsumer product
ABC Trading Recalls Children's Toys Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys
ABC Trading recalls toy headbands and electronic pet cages due to accessible button cell batteries that pose a risk of serious injury or death if ingested.
ABC TradingMay 21, 2026 - Stop using nowVehicle
BLUE BIRD VISION SCHOOL BUS (2027) recall — Equipment Adaptive/Mobility
Blue Bird recalls certain 2027 Vision school buses because wheelchair retractors may not lock, increasing injury risk. Free dealer inspection and repair available.
Blue BirdMay 20, 2026 - Lower riskMedical device
United Orthopedic Corp. recalls Brand Name: USTAR II Knee System Product Name: Hinge Box Trial, L, #1-6 and Hinge Box Trial, R, #1-6 Model/Catalog
United Orthopedic Corp. recalls USTAR II Knee System Hinge Box Trial models due to incomplete screw assembly preventing proper stem trail. Affected units include specific model numbers and lot codes.
USTAR IIMay 20, 2026
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