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- Stop using nowConsumer product
Flame King Recalls Hog 100-Pound Propane Cylinders Due to Fire Hazard
Flame King recalls Hog 100-pound propane cylinders due to a fire hazard from gas leaks. Stop using immediately and contact Flame King for a refund or replacement.
Flame KingMar 24, 2021 - Stop using nowConsumer product
Birdie Belay Devices Recalled Due to Risk of Injury; Made by Beal Sas
Beal Birdie Belay Devices with batch year "/19" pose injury risk. Stop using and get free replacement from Liberty Mountain.
BealMar 24, 2021 - Lower riskMedical device
Medtronic Inc. recalls VenaSeal Closure System
Medtronic recalls VenaSeal Closure System models SP-101 and VS-402/404 due to adhesive not advancing through delivery catheter. Affected units have specific serial numbers listed in the recall notice.
MedtronicMar 23, 2021 - Lower riskMedical device
Philips North America, LLC recalls Philips SureSigns VM4, VM6 and VM8 - Product Usage: patient monitors-for monitoring, recording and alarming of multiple
Philips recalls certain SureSigns VM4, VM6, and VM8 patient monitors sold in China for potential pediatric heart rate inaccuracies in high-rate scenarios.
PhilipsMar 23, 2021 - Lower riskMedical device
Sunstar Americas, Inc. recalls SUNSTAR Butler Clear Dip, 16 FL OZ, SKU #716PA
Sunstar recalls 16 fl oz Butler Clear Dip due to Burkholderia contaminans risk. Affected lots: 532952, 535180, 536513, 536514, 53948:551038, 551039. Stop using if contaminated.
SunstarMar 23, 2021 - Stop using nowMedical device
Bioseal Corporation recalls Bioseal, Central Line Dressing Kit, containing ChloraPREP Applicator 3 mL, REF: CVC009/20, Sterile EO, Single Use Only,
Bioseal recalls central line dressing kits with ChloraPREP applicator due to potential Aspergillus penicillioides growth that could breach packaging. Affected lots include 400521, 400514, and others. Stop using immediately.
BiosealMar 23, 2021 - Lower riskMedical device
Covidien Llc recalls Covidien Tri-Staple 2.0 Reinforced Intelligent Reload 60 mm Medium/Thick-For use with Signia stapling system. Staple
Covidien recalls Tri-Staple 2.0 Reinforced Intelligent Reload 60mm staples for potential sterility compromise due to extra laminate layer, risking patient infection or ethylene oxide exposure.
CovidienMar 23, 2021 - Use cautionVehicle
AUDI A3 (2020) recall — Air Bags
Audi is recalling certain 2015-2020 A3 models due to passenger air bag deactivation risk during crashes. Owners receive free repairs to fix the PODS system.
AudiMar 22, 2021 - Lower riskMedical device
QURA S.R.L. recalls Spectrum Medical Quantum Standard heat exchanger
Qura recalls Spectrum Medical Quantum Standard heat exchangers with specific batch numbers due to potential inadequate sterilization and lack of US 510(k) clearance.
QuraMar 22, 2021 - UnratedMedical device
Datascope Corp. recalls Cardiosave Rescue IABP - Product Usage: used to inflate and deflate intra-aortic balloons. It provides temporary
Datascope recalls Cardiosave Rescue IABP devices due to cybersecurity vulnerabilities that could disrupt hospital information systems. Affected models include 0998-00-0800-75, 0998-00-0800-83, and 0998-00-0800-85. No remedy is specified in the recall notice.
DatascopeMar 22, 2021 - Lower riskMedical device
Normand-Info S.A.S.U. recalls Normand Remisol Advance Data Manager is a software device that interfaces between laboratory information systems (LIS)
Normand recalls software devices that interface lab systems and instruments. Incorrectly programmed rules may cause erroneous lab results. Affected units have catalog numbers B08688, B2:22517, B35058, B74811, B92487.
NormandMar 22, 2021 - Lower riskMedical device
BIOPSYBELL S.R.L. recalls BPB medica CEMIX, PRODUCT NUMBER KVTMIXN, Vertebroplasty-Kyphoplasty cement mixing system
BIOPSYBELL recalls CEMIX vertebroplasty cement mixers due to potential unsterilized products. Affected units may pose infection risks if used without proper sterilization.
BIOPSYBELLMar 22, 2021 - UnratedDrug
Macleods Pharma Usa Inc recalls Candesartan Cilexetil Tablets, USP, 4 mg, 30-count bottles, Rx only, Manufactured for: Macleods Pharma USA, Inc.,
Macleods Pharma recalls 4mg Candesartan tablets due to failed impurities. Affected lots from ECD5908C to ECD5912A, expiring 07/2021 and 09/2021. Stop using if you have these specific lots.
MacleodsMar 22, 2021 - Lower riskDrug
Novo Nordisk Inc recalls Saxenda (liraglutide) Injection, 18 mg/3 mL (6 mg/mL), 1 x 3 mL Prefilled Pen, Sample. Not for Resale., Rx only, Novo
Novo Nordisk recalls Saxenda (liraglutide) samples due to improper cold storage causing potential product damage. Affected samples were stored below 32°F, risking cartridge and pen-injector damage.
Novo NordiskMar 22, 2021 - Stop using nowFood
Land O'Lakes, Inc. recalls Land O Lakes Queso Bravo White Cheese Dip with Jalapeno and Red Peppers. Net Wt 5 lbs. (2.26kg), UPC 34500-48238.
Land O'Lakes recalls 5 lb pouches of Queso Bravo White Cheese Dip due to potential metal contamination. Check your UPC and lot numbers.
Land O'LakesMar 22, 2021 - Stop using nowFood
Grace Kennedy Foods USA LLC recalls La Fe Brand Frozen Peppers and Onions 16 oz bags.
Grace Kennedy Foods recalls La Fe Brand Frozen Peppers and Onions due to plastic contamination. Check lot KR043021.
La FeMar 22, 2021 - Lower riskFood
Sea World, LLC recalls Crimson Snapper Fillet, Natural Cut CO Treated, Net WT 10 LBS, Size 10/12 oz
Sea World recalls natural cut crimson snapper fillets with decomposition risk. Products sold between 2022-11-27 and 2022-11-27 (best by date) may be unsafe due to fish decomposition.
Sea WorldMar 22, 2021 - Lower riskFood
Simply Delicious Inc. recalls Bobo's Maple Pecan Oat Bars, 3 oz., UPC 8 2926200021 0, Best By 7/30/21 or 7/31/21.
Simply Delicious recalls Bobo's Maple Pecan Oat Bars (3 oz, UPC 829262000210) due to peanuts found in bars. Consumers should check best by dates and contact for details.
Simply DeliciousMar 22, 2021 - Lower riskMeat & poultry
Avanza Pasta, LLC Recalls Beef and Poultry Products Produced Without Benefit of Inspection
USDA recalls 9,847 pounds of un-inspected beef and poultry pasta products from October 2019 to March 2021. Consumers urged not to consume these items due to lack of federal inspection.
Avanza PastaMar 20, 2021 - Lower riskFood
Avanti Frozen Foods Private Limited recalls 365 Whole Foods Market Farm Raised Cooked Shrimp 2 lbs/Ready- to - Serve Tail-On/Peeled & Deveined/41-55 Shrimp/lb NET
Avanti Frozen Foods recalls 365 Whole Foods Market Farm Raised Cooked Shrimp because one lot was mistakenly packaged as cooked. Consumers should check for production date code 91AS/22VN/175A on the clear plastic bag packaging.
Avanti Frozen FoodsMar 20, 2021 - Lower riskFood
Schlotterbeck & Foss, LLC recalls Taste of Inspirations Garlic Parmesan Wing Sauce
Schlotterbeck & Foss recalls Taste of Inspirations Garlic Parmesan Wing Sauce due to undeclared fish content. Consumers should check lot numbers and UPC codes for affected products.
Schlotterbeck & FossMar 20, 2021 - Lower riskMeat & poultry
FSIS Issues Public Health Alert for Beef and Lamb Products Produced Without Benefit of Inspection
FSIS public health alert: Beef and lamb products from Eastern Asia Trading Corporation produced without federal inspection are no longer available. Consumers are urged not to consume these products.
Eastern Asia Trading CorporationMar 19, 2021 - Use cautionVehicle
MERCEDES-BENZ GLC350E (2019) recall — Structure
Mercedes-Benz recalls 2019 GLC350e vehicles with potential front panel detachment due to improper bonding during repair. Owners must contact dealers for free front panel replacement.
Mercedes-BenzMar 19, 2021 - Use cautionVehicle
CHEVROLET 5500HD (2019) recall — Suspension
Isuzu recalls certain 2019 Chevrolet 5500HD vehicles with potential rear axle misalignment causing power loss and crash risk. Owners must have rear axle U-bolt nuts inspected and tightened free of charge by dealers.
IsuzuMar 19, 2021 - Use cautionVehicle
AIRSTREAM BASECAMP (2020) recall — Equipment
Airstream recalls 2017-2020 Basecamp travel trailers due to air conditioning mounting bolts that may loosen or break, causing the AC unit to separate and become a road hazard.
AirstreamMar 19, 2021 - Lower riskMedical device
GE Healthcare, LLC recalls Centricity Universal Viewer - Product Usage: intended to assist in the viewing, analysis, diagnostic interpretation,
GE Healthcare recalls Centricity Universal Viewer devices that may show incorrect patient comparisons when Cross Enterprise Display is enabled and Workflow Manager launches the viewer. Affected units have specific serial numbers and UDI codes.
GE HealthcareMar 19, 2021 - Lower riskMedical device
Baxter Healthcare Corporation recalls Spectrum IQ - Infusion Pump - Product Usage: intended to be used for the controlled administration of fluids.
Baxter recalls Spectrum IQ infusion pumps with serial numbers listed in the record due to a potentially defective AC power adapter that may fail over time.
BaxterMar 19, 2021 - Use cautionMedical device
GE Healthcare, LLC recalls Revolution CT
GE Healthcare recalls Revolution CT systems due to potential radiation dose inaccuracies. Affected units may deliver higher or lower radiation than prescribed, risking patient safety.
GE HealthcareMar 19, 2021 - Lower riskMedical device
Cytocell Ltd. recalls Chromosome X Alpha-Satellite in FITC Spectrum - Product Usage: Analyte Specific Reagents. Model: MPA3481
Cytocell recalls Chromosome X Alpha-Satellite in FITC Spectrum reagents (model MPA3481) due to possible false signals at 9q3: users may see extra locus-specific signals despite no cross-reactivity claims.
CytocellMar 19, 2021 - UnratedMedical device
Cardiac Assist, Inc recalls Protek Solo Venous Dilator Set: dilator, vessel, for percutaneous catheterization. Catalog #: 5840-2417 - LS Tandem
Cardiac Assist recalls 14 kits of Protek Solo Venous Dilator Set with incorrect packaging that could be distributed to patients. Affected units include specific catalog numbers and serial lots.
Cardiac AssistMar 19, 2021
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