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
34,893 found- Use cautionVehicle
ENTEGRA CORNERSTONE (2018) recall — Fuel System, Diesel
Entegra is recalling 2018 Cornerstone motorhomes with Cummins ISX 15L engines due to a potential fuel pump failure causing engine stalls and crash risk. Owners can get free fuel pump replacements.
EntegraJul 13, 2017 - Stop using nowMedical device
Bios S.r.l. recalls THERMI250 Radiofrequency System. Intended to provide heating for the purpose of elevating tissue temperature for
Bios recalls THERMI250 radiofrequency systems that emit RF energy after pause button is pressed. Affected units have specific serial numbers. Users should stop using immediately to prevent potential tissue damage.
BiosJul 13, 2017 - Lower riskMedical device
GE Medical Systems Information Technologies, Inc. recalls CARESCAPE Patient Data Module (PDM) v2.6 software used with CARESCAPE Monitors B850, B650, and B450 v2.0.7 or earlier
GE Medical Systems recalls CARESCAPE Patient Data Module v2.6 software used with CARESCAPE Monitors B850, B650, and B450 v2.0.7 or earlier. This software fails to produce visual or audible alarms for impedance respiration apnea events, potentially missing critical patient safety alerts.
GE Medical SystemsJul 13, 2017 - Use cautionMedical device
Medtronic Vascular Galway DBA Medtronic Ireland recalls Solarice Rapid Exchange Balloon Dilatation Catheter, a Percutaneous Transluminal Coronary Angioplasty (PTCA) Rapid
Medtronic recalls Solarice Rapid Exchange Balloon Dilatation Catheters due to stylette removal difficulties. Affected models include SLC2525X, SLC3520X, and others with specific lot numbers. Consumers should check their product details and contact Medtronic for guidance.
MedtronicJul 13, 2017 - Lower riskMedical device
In2Bones, SAS recalls Non-Locking screws in the following lengths: (a) NEO(R) 0.27 - 10 mm, REF W27 ST010 (b) NEO(R) 0.27 - 12 mm, REF W27
In2Bones recalls specific lengths of Non-Locking screws used in distal radius fracture repairs due to reported perioperative breakages during surgery.
In2BonesJul 13, 2017 - Use cautionMedical device
Microline Surgical, Inc. recalls The ReNew Reusable Grasper and Dissector Tips are to be used with the ReNew Laparoscopic Handpieces and they are
Microline recalls ReNew reusable grasper and dissector tips used with laparoscopic handpieces due to risk of heat-shrink tube splitting during autoclave sterilization, potentially causing burns during surgery.
MicrolineJul 13, 2017 - Lower riskMedical device
Bomimed recalls BOMImed Disposable Fiber Optic Medium Laryngoscope Handle. Each handle is packaged in an individual peel pouch, 20
Bomimed disposable laryngoscope handles may flicker during use. Affected models include OL-334L6 with lots 2216, 3016, 4016, 4816. Recalled due to potential intermittent lighting.
BomimedJul 13, 2017 - UnratedMedical device
Pentax of America Inc recalls Video Cystoscope models ECY-1570 and ECY-1570K
Pentax recalls video cystoscope models ECY-1570 and ECY-1570K due to lack of FDA 510(k) premarket clearance. Affected units have specific serial numbers listed in the recall notice.
PentaxJul 13, 2017 - Lower riskFood
Cafe Spice GCT DBA Zaika Flavors of India Inc. recalls Whole Foods Market Thai Shrimp Salad, Net Wt. 14 oz.. packaged in a clear clamshell container (refrigerated)
Whole Foods Market Thai Shrimp Salad (14 oz) recalled due to incorrect back label showing Chicken Florentine Salad information. Consumers should check product details and contact retailer for replacement.
Cafe SpiceJul 13, 2017 - Stop using nowConsumer product
YSN Imports Recalls Refillable Propane Cylinders Due to Fire, Explosion Hazards
YSN Imports recalls Flame King, Little Kamper, and U-Haul refillable propane cylinders due to fire and explosion hazards from propane leaks. Consumers should stop using and get a refund or replacement.
YSN ImportsJul 13, 2017 - Use cautionConsumer product
TOMY Recalls Munching Max Chipmunk Toys Due to Laceration Hazard
TOMY recalls Lamaze Munching Max chipmunk stuffed toys with item L27578 due to sharp parts causing lacerations. Consumers should stop using and get a free replacement.
TOMYJul 13, 2017 - Stop using nowConsumer product
TJX Recalls Glass Beer Mugs Due to Burn and Laceration Hazards; Sold Exclusively at HomeGoods Stores
HomeGoods recalls 16.9-oz glass beer mugs sold May-June 2017 due to burn and laceration risks when heated or used with hot liquids.
HomeGoodsJul 13, 2017 - Use cautionVehicle
WINNEBAGO JOURNEY (2018) recall — Equipment
Winnebago is recalling 2018 Journey motorhomes with potentially clogged Kidde fire extinguishers that may fail during fires, increasing injury risk. Owners can get free replacements from Kidde.
WinnebagoJul 12, 2017 - Lower riskMedical device
DePuy Orthopaedics, Inc. recalls CORAIL HIGH OFFSET STEM Collarless SIZE 14
DePuy recalls CORAIL HIGH OFFSET STEM Collarless Size 14 (Part No. L20314, Lot No. 5292130) due to incorrect product being shipped in the package. Consumers should check their order details.
DePuyJul 12, 2017 - Stop using nowMedical device
Philips North America, LLC recalls MRx Defibrillator Model # M3535A & M3536A, UDI 00884838000018(21)US00601969 Product Usage: The HeartStart MRx is for
Philips recalls HeartStart MRx defibrillators (models M3535A & M3536A) due to a defective component that may prevent shock delivery in AED mode. Affected units have specific serial numbers.
PhilipsJul 12, 2017 - Lower riskMedical device
Biomerieux Inc recalls VITEK¿ 2 Compact 30, REF numbers: 27530 and 27530R (clinical), and 27630 and 17630R (industry) software and reagent
Biomerieux recalls VITEK 2 Compact 30 software and reagent cards that may stay in preliminary status after ejection, preventing further processing. Affected units were updated to software version 8.01.
BiomerieuxJul 12, 2017 - UnratedDrug
Pfizer Inc. recalls Deferoxamine Mesylate for injection, USP, Single-use Vial, 500 mg/vial, 10 mL vial. Intravenous, Intramuscular,
Pfizer recalls Deferoxamine Mesylate injection vials due to color change impurity during manufacturing. Affected lots may pose safety risks; contact Pfizer for details.
PfizerJul 12, 2017 - UnratedDrug
Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical recalls Testosterone Cypionate + Progesterone, 200 mg/ 2.5 mg/mL ,10 mL amber glass vials, Rx Only, Compounded by AXIA
Axia Pharmaceutical recalls testosterone cypionate and progesterone vials due to CGMP deviations. Affected lots may pose safety risks; check your product details.
Axia PharmaceuticalJul 12, 2017 - Use cautionDrug
Akorn Inc recalls Halyard 24-Hour Oral Care Kit q2, contains 2x15 mL Unit Dose Cups 0.12% Chlorhexidine Gluconate Oral Rinse.
Akorn recalls Halyard 24-Hour Oral Care Kits due to chlorhexidine crystallization and subpotent results. Check lot numbers and expiration dates.
HalyardJul 12, 2017 - Stop using nowFood
Stutzman Farms recalls STUTZMAN FARMS Savory Sprouted Spelt Crackers Net Wt. .30 LB. (136 g)
Stutzman Farms recalls Savory Sprouted Spelt Crackers because wheat is missing from the allergen statement. Check your pantry.
Stutzman FarmsJul 12, 2017 - Stop using nowConsumer product
TriggerTech Recalls Crossbow And Rifle Triggers Due to Injury Hazard
TriggerTech recalls carbide crossbow and rifle triggers with risk of unintended discharge due to cracked rollers. Consumers must stop using and return for free stainless steel replacement or refund.
TriggerTechJul 12, 2017 - Use cautionConsumer product
Core Health & Fitness Recalls Exercise Machines Due to Impact Hazard (Recall Alert)
Core Health & Fitness recalls five exercise machine styles due to risk of carriage falling and causing injury. Affected machines have 'Inspiration' or 'Star Trac'/'Nautilus' labels. Consumers must stop use and get free repair.
Core Health & FitnessJul 12, 2017 - Use cautionVehicle
SUBARU CROSSTREK (2018) recall — Service Brakes
Subaru recalls 2018 Crosstrek vehicles with faulty floor mat retention brackets that could move and interfere with pedals, increasing crash risk. Owners should contact Subaru for free inspection and replacement.
SubaruJul 11, 2017 - Use cautionMedical device
Exactech, Inc. recalls Exactech GPS Total Shoulder Application 3.2mm Vix Bit Orthopedic surgical tool
Exactech recalls 3.2mm Vix Bit orthopedic surgical tools due to fracture risk during use. Affected items have specific catalog and lot numbers. Consumers should contact Exactech for details.
ExactechJul 11, 2017 - Lower riskMedical device
Olympus Scientific Solutions Americas recalls Olympus Scientific Solutions Americas Corporation ( OSSA ) Model: VANTA Analytical X-Ray System, X-Ray Fluorescence
Olympus Scientific Solutions recalls VANTA Analytical X-Ray Systems (VCR/VMR models) that may fail to stop tests when no sample is present, risking incomplete analysis.
Olympus Scientific SolutionsJul 11, 2017 - Lower riskMedical device
Philips Medical Systems (Cleveland) Inc recalls Brilliance iCT - Model 728306 Computed Tomography X-ray systems
Philips recalls Brilliance iCT CT scanners with software version 4.1.6 due to scan start position, data acquisition, and other function errors that could lead to improper imaging.
Philips Medical SystemsJul 11, 2017 - UnratedDrug
Dr. Reddy's Laboratories, Inc. recalls Pravastatin Sodium Tablets, USP, 10 mg, packaged in a) 90-count bottles (NDC 55111-229-90) and b) 500-count bottles
Dr. Reddy's recalls 10mg Pravastatin tablets with high impurity levels that may cause health risks. Affected lots C700220 (expiring June 2018) in 90-count and 500-count bottles.
Dr. Reddy'sJul 11, 2017 - Stop using nowConsumer product
Superpedestrian Recalls Electric Bicycle Conversion Wheels Due to Fall and Crash Hazards (Recall Alert)
Recalled Copenhagen wheels (serial numbers 01031708600020000000-01031710400250000000 for multi-speed, 02031708600020000000-02031710400250000000 for single-speed) pose fall and crash risks. Consumers must stop using and get free replacements.
SuperpedestrianJul 11, 2017 - Lower riskMedical device
AMEDA, INC. recalls Purely Yours Breast Pump. Model 17070PMW and Model 17070ACA. Intended to express and collect the mother s milk from the
AMEDA recalls Purely Yours breast pumps (Model 17070PMW/17070ACA) with UK power adapters that may cause electrical issues. Affected units include Lot 7E058 and Lot 7E308.
AMEDAJul 10, 2017 - Lower riskMedical device
Ortho Clinical Diagnostics Inc recalls VITROS Chemistry Products Performance Verifier is used as an assayed control to monitor the performance on VITROS
Ortho Clinical Diagnostics recalls VITROS Performance Verifier II Lot K4852 due to refrigerated stability problems for AST analyte. Affected units may not remain stable after 6 months in the fridge.
Ortho Clinical DiagnosticsJul 10, 2017
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83,389 recalls tracked · 71,917 explained in plain English · 10,946 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.