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
35,021 found- Lower riskMedical device
WELL LEAD MEDICAL CO. LTD recalls SunMed Tracheal Tube, Size 2.5; Model Number: 1-7333-25
SunMed recalls tracheal tubes size 2.5 (model 1-7333-25) due to suction catheter not passing samples smoothly. Affected units include specific lot numbers from 2021-2026.
SunMedJul 31, 2026 - Lower riskMedical device
Medline Industries, LP recalls Convenience kits ANESTHESIA PAIN PK LEAGUE DYNJ67925A
Medline recalls anesthesia pain kits with potential open seals in sterile pouches that could cause patient infections if used without proper sterility checks.
MedlineJul 31, 2026 - Lower riskMedical device
Bayer Medical Care, Inc. recalls MEDRAD¿ Stellant FLEX Syringe Kit used with Stellant FLEX CT Injection System; Catalog number: FLEXS-150-QFT;
Bayer Medical Care recalls Stellant FLEX Syringe Kit (FLEXS-150-QFT) due to potential improper sterilization during manufacturing. Affected units may pose infection risks if used.
Bayer Medical CareJul 31, 2026 - Use cautionMedical device
Johnson & Johnson Surgical Vision, Inc. recalls HEALON EndoCoat PRO, REF: 10300012 (US/CAN) HEALON DUET PRO II, REF: 10300016 (US/CAN) HEALON EndoCoat PRO, REF:
Johnson & Johnson Surgical Vision recalls HEALON EndoCoat PRO and HEALON DUET PRO II products due to risk of corneal abrasion or eye damage if cannula is forced during cataract surgery.
Johnson & Johnson Surgical VisionJul 31, 2026 - Lower riskDrug
Liebel-Flarsheim Company LLC recalls Optiray Imaging Bulk Package-350, Ioversol Injection 74%, 350 mg/mL Organically Bound Iodine, 500 mL Multiple-Dose
Liebel-Flarsheim recalls Optiray Imaging Bulk Package-350 (Ioversol 74%) due to potential particulate matter in the injection solution. This could cause blockages or reactions if injected. Affected units have NDC 0019-1333-65 and lot # 25ZF3670.
Liebel-FlarsheimJul 31, 2026 - Use cautionVehicle
CHEVROLET SILVERADO EV (2026) recall — Wheels
General Motors recalls 2026 Chevrolet Silverado EVs with cracked steel wheels that could cause loss of control and crash risk. Owners must have wheels inspected and replaced free by dealers.
ChevroletJul 30, 2026 - Use cautionMeat & poultry
FSIS Issues Public Health Alert for Chicken Salad Product that May Be Contaminated with Listeria
U.S. Department of Agriculture alerts consumers not to eat Curry Chicken Salad products from Mary's Harvest Fresh Foods that may be contaminated with Listeria monocytogenes. Products were produced in Oregon and Washington and no recall was requested as they are no longer available for purchase.
Mary's Harvest Fresh FoodsJul 30, 2026 - Use cautionVehicle
HONDA CMX500 (2017) recall — Steering
Honda recalls 2017-2023 CMX500 and CMX300 motorcycles due to handlebar lock screw detaching, which can interfere with steering and increase crash risk. Owners must have the screw replaced by dealers.
HondaJul 30, 2026 - Use cautionVehicle
RAM 1500 (2019) recall — Seat Belts
Chrysler recalls certain 2019-2026 Ram 1500 vehicles with improperly installed seat belt buckle anchors that may fail during crashes, risking injury. Owners will receive free repairs by August 2026.
ChryslerJul 30, 2026 - Lower riskMedical device
Howmedica Osteonics Corp. recalls AXLE PIN ASSY LARGE ELBOW COBALT CHROME Catalog No. C-M112-2-500 Orthopaedic implant components manufactured from
Howmedica Osteonics recalls cobalt chrome elbow implants manufactured with aged polyethylene that may cause increased wear debris, requiring revision surgery. Affected units have catalog number C-M112-2-500 and UDI-DI lot P22E159.
HowmedicaJul 30, 2026 - Use cautionMedical device
Datex-Ohmeda, Inc. recalls Aisys, Datex-Ohmeda anesthesia system, Part Number 1011-9050-000
Datex-Ohmeda recalls Aisys anesthesia systems with specific part numbers due to risk of automatic transition to Alternate O2 control, which may interrupt anesthetic delivery and require clinician intervention to prevent decreased anesthetic effect.
Datex-OhmedaJul 30, 2026 - Lower riskMedical device
GE Medical Systems Information Technologies Inc recalls Carescape Central Station CSCS V3 MAS800 Desktop Part Number 5867474-04, 5867474-13 Product code STU CSCS V3 MAI800
GE Medical Systems recalls Carescape Central Station V3 MAS800 desktop units with part numbers 5867474-04 and 5867474-13. The device may delay patient monitoring for up to 3 minutes after restart, risking missed critical health events.
GE Medical SystemsJul 30, 2026 - Stop using nowFood
Ukrop's Homestyle Foods LLC recalls Bread Pudding with Vanilla Sauce NET WT 13.8 OZ (39g) UPC 7 22515 28044 8 Ukrop's Homestyle Foods, LLC Richmond, VA
Ukrop's recalls Bread Pudding with Vanilla Sauce (13.8 oz) due to metal fragments. Consumers should check UPC 7 22515 28044 8 and return affected products.
Ukrop'sJul 30, 2026 - Use cautionMedical device
Bard Access Systems, Inc. recalls BD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK, BD Needle Kit for Powered Driver 25mm x 15Ga, REF:
Bard recalls specific needle kits for powered drivers due to risk of obturator locking to needle hub, potentially causing delayed therapy during emergency IV access.
BardJul 30, 2026 - UnratedDrug
Heritage Pharmaceuticals Inc recalls CLINDAMYCIN PALMITATE HYDROCHLORIDE FOR ORAL SOLUTION, USP, 75 mg/5 mL, Rx Only, 100 mL, Distributed by: Avet
Heritage Pharmaceuticals recalls Clindamycin Palmitate Oral Solution (75 mg/5 mL) due to foreign particles and white flakes. Check lot #2411550.
Heritage PharmaceuticalsJul 30, 2026 - Use cautionVehicle
CADILLAC ESCALADE IQ (2026) recall — Electrical System
General Motors recalls 2026 Cadillac Escalade IQ vehicles with a loose battery component that could cause fire. Owners must have the high voltage battery replaced free by dealers.
CadillacJul 30, 2026 - Use cautionVehicle
WINNEBAGO EKKO (2025) recall — Equipment
Winnebago recalls 2024-2025 Ekko motorhomes with potential carbon monoxide poisoning risk if generator runs in enclosed spaces like garages. Owners must park outside until software fix is applied.
WinnebagoJul 30, 2026 - Stop using nowConsumer product
Woodure Toddler Kitchen Step Stools Recalled Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards; Imported by Shenzhen Muqiqu Creative Development
Woodure toddler kitchen step stools (models WD1764, WD1357, WD1720) recalled due to collapse risk and child entrapment. Stop using immediately to prevent serious injury or death.
WoodureJul 30, 2026 - Stop using nowConsumer product
Trsmima Zipline Kits and Zipline Spring Brakes Recalled Due to Fall and Collision Hazards; Manufactured by Trsmima
Trsmima recalls backyard zipline kits and spring brakes due to risk of falls and collisions from detached components or failure to slow riders. Consumers must stop using and destroy items for full refund.
TrsmimaJul 30, 2026 - Stop using nowConsumer product
Recall of Cpzzkq Baby Loungers Expanded Due to Risk Serious Injury or Death from Suffocation Hazard; Violate Mandatory Standard for Infant Support Cushions; Sold on Amazon by CetoPMax
Recall of 195 Cpzzkq baby loungers sold on Amazon by CetoPMax due to suffocation hazard from breathing obstruction. Stop using immediately and return for refund.
CetoPMaxJul 30, 2026 - Stop using nowConsumer product
OCOOPA Direct Recalls 1.5 Million Rechargeable Hand Warmers Due to Risk of Serious Injury or Death from Fire and Burn Hazards; One Death Reported; Imported by Shenzhen Street Cat Technology
OCOOPA Direct recalls 1.5 million rechargeable hand warmers due to fire and burn hazards from overheating lithium-ion batteries. One death reported in 2026.
OCOOPAJul 30, 2026 - Stop using nowConsumer product
Mommy's Baby Lovely Deluxe Baby Doll Playsets Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violate Small Parts Ban; Sold on Temu by TOYHW
Mommy's Baby Lovely Deluxe Baby Doll Playsets (model NEW31:9A) sold on Temu pose choking hazard for children under 3. Recalled items must be discarded and refunded via email proof.
Mommy's BabyJul 30, 2026 - Stop using nowConsumer product
Mangohood Direct Kids Kitchen Standing Towers Recalled Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards; Imported by Hangzhou Xinyanchuangxin
Mangohood Direct recalls Model LT003 kids kitchen standing towers due to tip-over and entrapment risks. Stop using immediately; free repair parts available.
Mangohood DirectJul 30, 2026 - Stop using nowConsumer product
Joyin Expands Recall of Sloosh Dive Sticks Due to Risk of Serious Injury from Impalement; Violate Federal Dive Sticks Ban
Joyin recalls Sloosh dive sticks (models 40041, 40003, 16154) due to impalement risk in shallow water. Stop using immediately to prevent serious injuries.
JoyinJul 30, 2026 - Stop using nowConsumer product
Jake's Fireworks Recalls World Class Fireworks "Skull Strobe" Rockets Due to Risk of Serious Injury from Explosion and Burn Hazards
Jake's Fireworks recalls Skull Strobe rockets that can explode prematurely, causing injury. Consumers must stop using and return for refund.
Jake's FireworksJul 30, 2026 - Stop using nowConsumer product
Heated Sherpa Throws and Blankets Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Sold on Amazon by OCTROT
OCTROT electric throws and blankets with detachable cords risk fire, burns or shock. Stop using immediately and destroy products by cutting cord in half.
OCTROTJul 30, 2026 - Stop using nowConsumer product
HARPPA Recalls Nordi Toddler Tower Stools Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards
HARPPA recalls Nordi foldable toddler tower stools due to collapse risk and entrapment hazards. Stop using immediately to prevent serious injury or death.
HARPP: NordiJul 30, 2026 - Stop using nowConsumer product
Golden Link Recalls Fantastic Four Cups and Captain America Popcorn Helmet Containers with LED Lights Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violate Mandatory Standard for Consumer Products with Button Cell Batteries
Golden Link recalls Fantastic Four cups and Captain America popcorn helmets sold at theaters due to button cell battery ingestion risks. Stop using immediately.
Golden LinkJul 30, 2026 - Stop using nowConsumer product
Galanz Americas Recalls Retro Refrigerators Due to Risk of Serious Injury or Death from Fire and Burn Hazards; One Death Reported
Galanz recalls retro refrigerators from Dec 2018-2020 with model numbers BCD-215V-62H, GLR76TRDER, GLR76TBKER, GLR76TBEER, or GLR76TWEER due to fire and burn hazards from internal electrical short circuits.
GalanzJul 30, 2026 - Stop using nowConsumer product
BenQ America Recalls GV31 Portable Projectors Due to Risk of Serious Injury or Death from Fire and Burn Hazards
BenQ recalls GV31 portable projectors due to lithium-ion battery overheating risks. Consumers must stop using immediately and return for free repair or replacement.
BenQJul 30, 2026
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83,609 recalls tracked · 72,041 explained in plain English · 10,977 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.