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
34,943 found- UnratedMedical device
Medtronic Sofamor Danek USA Inc recalls Medtronic CD HORIZON Spinal System is intended to help provide immobilization and stabilization of spinal segments as
Medtronic recalls CD HORIZON Spinal System screws with incorrect 5.5mm marking (actual 5.0mm) that could lead to improper spinal fusion. Affected units sold in 2023 with specific lot numbers.
MedtronicJul 9, 2018 - Lower riskMedical device
Merit Medical Systems, Inc. recalls ChloraPrep With Tint, 2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA) Patient Preoperative
Merit Medical recalls ChloraPrep With Tint patient preop solution due to nonsterile bulk product shipped to customers. This may pose infection risks during surgery preparation.
Merit MedicalJul 9, 2018 - Use cautionMedical device
Sorin CRM SAS recalls Sorin Platinium CRT-D 1711 DF-1, Sterile EO. Implantable Cardiac Defibrillator and Resynchronization Therapy
Sorin recalls specific Platinium CRT-D 1711 DF-1 defibrillators due to potential overconsumption causing loss of pacing and sensing, risking missed arrhythmia detection.
SorinJul 9, 2018 - Lower riskDrug
Mylan Pharmaceuticals Inc. recalls Triamterene and Hydrochlorothiazide Tablets, USP 37.5 mg/25 mg, 100-count bottle, Rx only, Mylan Pharmaceuticals, Inc.
Mylan recalls 100-count Triamterene-Hydrochlorothiazide tablets (37.5mg/25mg) due to subpotent drug levels. Rx-only product with specific lot number and expiration date.
MylanJul 9, 2018 - Lower riskMeat & poultry
Recall Notification Report 059-2018 (Beef Jerky Products)
Recall of 102 pounds of Tillamook Teriyaki Beef Jerky due to misbranding; products may contain unlabeled MSG. Consumers should check labels for lot code 11588 and best by date 03/09/19.
Tillamook Country SmokerJul 6, 2018 - Use cautionVehicle
FERRARI 458 (2012) recall — Air Bags
Ferrari is recalling 2012 458 models with potentially dangerous air bags that could explode in crashes, risking serious injury or death. Owners must have the air bag replaced free by July 19, 2018.
FerrariJul 6, 2018 - Use cautionVehicle
MOBILITY VENTURES MV-1 (2016) recall — Exterior Lighting
Mobility Ventures is recalling 2015-2016 MV-1 vehicles with faulty turn signals that may not communicate driver intentions, increasing crash risk. Owners must update software to fix the issue.
Mobility VenturesJul 6, 2018 - Use cautionVehicle
VOLKSWAGEN ATLAS (2018) recall — Seat Belts
Volkswagen recalls 2018 Atlas vehicles with potentially damaged seat belt buckles that could release unexpectedly during crashes, risking injury. Owners must have buckles inspected and replaced if needed.
VolkswagenJul 6, 2018 - Use cautionVehicle
SPARTAN K2 (2019) recall — Tires
Spartan is recalling certain 2016-2019 K2 motorhome chassis due to tag axle tire damage from DEF fill bracket contact, which may cause a crash. Owners must have the bracket modified for free.
SpartanJul 6, 2018 - Use cautionVehicle
KEYSTONE COUGAR (2019) recall — Equipment
Keystone is recalling 2018-2019 Cougar trailers with propane grills that may overheat, causing fire. Owners must replace wooden grill assembly with metal.
KeystoneJul 6, 2018 - Use cautionMedical device
Neotract Inc recalls UroLift System REF Catalog Number: UL400-4 Tray Contents: UroLift System with Handle Release Tool STERILE R CE 0050
Neotract recalls UroLift System REF UL400-4 due to risk of failed implant delivery, potentially causing treatment delays or incomplete procedures. Affected units include specific catalog numbers and lots.
NeotractJul 6, 2018 - Lower riskMedical device
3M Company - Health Care Business recalls 3M Fast Release Varnish, 5% Sodium Fluoride, Mint Flavor, Rx Only, single use. 200 pack, with each package containing 1
3M recalls 200-pack of Mint Flavor Fast Release Varnish due to an unpleasant flavor caused by a manufacturing error. This Rx-only product may contain extraneous material affecting taste.
3MJul 6, 2018 - Lower riskMedical device
Smiths Medical ASD Inc. recalls smiths medical portex First Breath Adult Nasal Cannula, REF 001289, Curved Flared Tips, 213 cm (7 ft.) Tubing,
Smiths Medical recalls adult nasal cannulas with transposed 'Manufactured' and 'Use By' labels, risking expired product before manufacturing. Consumers should check labels for lot numbers 1703171A or 1705152A.
Smiths MedicalJul 6, 2018 - Use cautionFood
Earthrise Nutritionals Llc recalls Earthrise Natural Spirulina; Net Weight: 20.0 kg( 44.0 lbs); Double bag sealed - 1 bag per box. UPC: 0 32602 99040 3
Earthrise Nutritionals recalls 20kg spirulina with possible small metal pieces from sifter screens. Check lot numbers 17950-17983 and use by dates 8/22/2021 to 9/3/2021.
EarthriseJul 6, 2018 - Use cautionConsumer product
Sandoz and Novartis Recall Prescription Drug Blister Packages Due to Failure to Meet Child-Resistant Closure Requirements
Recalled prescription drug blister packages from Sandoz and Novartis lack child-resistant closures, posing poisoning risk for children. Consumers should secure packages out of children's reach and contact manufacturers for instructions.
Sandoz and NovartisJul 6, 2018 - Stop using nowConsumer product
Camso Recalls Dirt to Snow Bike Conversion Kits Due to Crash and Impact Hazards
Camso recalls dirt-to-snow bike conversion kits due to loosening brake bolts. Stop using immediately and contact a dealer for a free repair.
CamsoJul 6, 2018 - Use cautionMedical device
Pro-Med Instruments Gmbh recalls DORO LUCENT Transitional Member, REF 1101.026 Component of headrest system used in open and percutaneous craniotomies
Pro-Med recalls DORO LUCENT Transitional Member (REF 1101.026) used in spinal and brain surgeries due to potential headrest system failure. Affected units have specific serial numbers listed.
Pro-Med InstrumentsJul 5, 2018 - Use cautionMedical device
CTL Medical Corporation recalls CTL Medical Hex Driver, 1/4" Square QC, 4.0 Ratcheting Ref 015.7050
CTL Medical recalls 1/4" Square QC Hex Drivers with serial numbers 7EQAB-D and 7ATAB-D due to risk of anti-toggle ring separating during surgery, potentially causing screw failure.
CTL MedicalJul 5, 2018 - Lower riskDrug
Teva Pharmaceuticals USA recalls Fluocinolone Acetonide Topical Solution, USP, 0.01%, 60 mL bottle, Rx Only, Manufactured by: Actavis Laboratories UT,
Teva recalls 0.01% Fluocinolone Acetonide Topical Solution 60mL bottles due to failed impurities and degradation tests. This may affect drug safety and efficacy. Contact Teva for details.
Teva PharmaceuticalsJul 5, 2018 - Lower riskDrug
Sanofi-Aventis U.S. LLC recalls Admelog Solostar (insulin lispro injection), 100 units/ mL (U-100) injection, packaged in 3mL prefilled pens, 1 pen per
Sanofi recalls Admelog Solostar insulin pens that may not have been shipped at proper temperature, risking insulin effectiveness. Affected units include specific lot numbers and expiration dates.
SanofiJul 5, 2018 - UnratedDrug
The Hain Celestial Group, Inc. - Worldwide HQ recalls alba BOTANICA sport mineral sunscreen (titanium dioxide 7.0% and zinc oxide 9.0%), spf 45, 170 g (6 oz) tubes packaged
The Hain Celestial Group recalls alba BOTANICA sport mineral sunscreen tubes because the package contains the wrong product formulation. Check your lot codes.
alba BOTANICAJul 5, 2018 - Stop using nowFood
YWAM Faith Harvest Helpers recalls Canned Salmon in unlabeled 8oz metal cans. Cans are packaged into a case of 92 cans. The case label is read: "Canned
YWAM Faith Harvest Helpers recalls unlabeled canned salmon due to lack of scheduled manufacturing processes for low-acid foods.
YWAM Faith Harvest HelpersJul 5, 2018 - Lower riskFood
Gourmet International Inc. recalls SPARKLING POMEGRANETE JUICE DRNK, 6/34 oz., glass bottles
L'ITALY Sparkling Pome:granate juice bottles may leak due to faulty caps. Recalled products include all 6/34 oz glass bottles with specific lot codes. Consumers should check labels for affected items.
L'ITALYJul 5, 2018 - Use cautionMedical device
Medtronic Inc. recalls Guardian Connect App CSS7200 used on the iPhone, iPad, and iPod Touch devices.
Medtronic recalls Guardian Connect App CSS7200 for iPhone/iPad/iPod Touch. The app may close without alerting users to hypoglycemic or hyperglycemic events, risking missed blood sugar alerts.
MedtronicJul 4, 2018 - Use cautionVehicle
NISSAN JUKE (2012) recall — Fuel System, Gasoline
Nissan recalls 2011-2012 Juke models with potential fuel leaks that could cause fire if near ignition sources. Owners must have fuel pressure sensor tightened by dealers.
NissanJul 3, 2018 - Stop using nowVehicle
THOMAS BUILT BUSES MINOTOUR (2018) recall — Equipment Adaptive/Mobility
DTNA recalls 2007-2018 Thomas Minotour school buses with wheelchair lifts that may operate while the vehicle is in Neutral or Drive.
Thomas Built BusesJul 3, 2018 - Use cautionVehicle
THOMAS BUILT BUSES MINOTOUR (2018) recall — Equipment Adaptive/Mobility
Daimler Trucks North America is recalling certain 2007-2018 Thomas Built Buses Minotour transit buses with wheelchair lifts that may operate when the vehicle is not in Park, posing injury risk.
Thomas Built BusesJul 3, 2018 - Use cautionVehicle
BMW X3 (2018) recall — Structure
BMW is recalling certain 2018 X3 models due to potential spoiler detachment while driving, increasing crash risk. Owners must have spoiler inspected by dealers.
BMWJul 3, 2018 - Lower riskMedical device
Abbott Vascular recalls PLUS 30 PRIORITY PACK Accessory Kit Product Usage: Is recommended for use during vascular procedures in conjunction
Abbott Vascular recalls PLUS : 30 PRIORITY PACK Accessory Kit due to potential incorrect expiration entry for one lot. This may affect medical device safety during vascular procedures.
Abbott VascularJul 3, 2018 - Lower riskMedical device
ConvaTec, Inc recalls AbViser AutoValve IAP (intra- abdominal pressure) Monitoring Device, Patient mount: a) REF ABV300, b) REF ABV301
ConvaTec recalls AbViser AutoValve IAP monitoring devices (REF ABV300/ABV301) due to potential pinhole breaches in sterile barriers. Affected units may leak fluid during use.
ConvaTecJul 3, 2018
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