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
34,959 found- Lower riskFood
Topnotch Foods Inc recalls Topnotch Foods Italian Bread Crumbs: 10 lb. Net Wt.. 10 lbs. (4.54 Kg) Item number 10008: Vernon, CA 90058 Correct
Topnotch Foods recalls Italian Bread Crumbs due to undeclared soy lecithin in California inspections. This may pose a risk for people with soy allergies. Check product label for item number 10008.
Topnotch FoodsApr 30, 2019 - Lower riskFood
Paximadi Co. LLC recalls Biscotti-Plain. Product is bulk packed in a master cardboard case and each master case contains either 48 or 36
Paximadi Co. LLC recalls bulk Biscotti-Plain due to missing milk declaration on master case label. Consumers should check for 48 or 36 biscotti per master case with delivery date 4/24.
PaximadiApr 30, 2019 - Stop using nowConsumer product
Tween Brands Recalls Light Up Bed Canopies Due to Fire and Burn Hazards; Sold Exclusively at Justice (Recall Alert)
Tween Brands recalls Justice Light Up bed canopies due to fire and burn risks from overheating lights. Affected models sold at Justice stores; return for refund or credit.
Tween BrandsApr 30, 2019 - Use cautionVehicle
RAM PROMASTER (2019) recall — Seats
New England Wheels recalls 2014-2019 Ram Promaster 2500/3500 vehicles with Freedman Go-ES Foldaway seats due to potential seat back movement in crashes, increasing injury risk.
New England WheelsApr 29, 2019 - Use cautionVehicle
AIRSTREAM FLYING CLOUD (2020) recall — Equipment
Airstream is recalling 2020 Flying Cloud travel trailers due to spare tire carrier detachment risk. The recall addresses a potential hazard where the spare tire carrier may separate from the vehicle while moving, increasing crash risk.
AirstreamApr 29, 2019 - Lower riskMedical device
Philips North America, LLC recalls Philips IntelliBridge System configured with a regional setting which uses a comma for a decimal separator: 866417
Philips recalls IntelliBridge System models with regional comma decimal setting causing infusion data to be recorded 100 times faster than actual rates. Affected units may have inaccurate patient records.
PhilipsApr 29, 2019 - Lower riskMedical device
Philips Ultrasound Inc recalls Philips EPIQ and Affiniti Ultrasound Systems with software version 4.0: Models EPIQ 5G, EPIC 5C, EPIQ 5W, EPIQ 7G, EPIC
Philips recalls EPIQ and Affiniti ultrasound systems with software version 4.0 due to potential patient folder mix-ups during editing. Affected models include EPIQ 5G, EPIC 5C, and others. No immediate action needed but software update recommended.
PhilipsApr 29, 2019 - Lower riskMedical device
COVIDIEN LLC recalls MAHURKAR and Argyle acute hemodialysis catheters, Material numbers 8813793009 8813793013 8813794005 8813794009
Covidien recalls MAHURKAR and Argyle acute hemodialysis catheters with incorrect priming volume values that may lead to improper catheter filling during dialysis.
CovidienApr 29, 2019 - Lower riskMedical device
KaVo Dental Technologies LLC recalls DEXIS Titanium Intraoral Sensor Product Usage: The DEXIS Titanium Intraoral Sensor is a USB-driven sensor which is
KaVo recalls specific DEXIS Titanium Intraoral Sensors due to incorrect calibration files causing reduced image quality. Affected units have serial numbers listed in the recall notice.
KaVoApr 29, 2019 - Lower riskDrug
Pfizer Inc. recalls Relpax (eletriptan HBr) 40 mg, a) 12 tablets 2 cards x six 40 mg tablets per blister pack, NDC 0049-2340-05; b) 6
Pfizer recalls Relpax 40mg tablets due to a labeling error showing 20mg instead of 40mg per tablet. This may cause incorrect dosing. Affected products have specific NDC numbers and expiration dates.
PfizerApr 29, 2019 - Lower riskFood
FIDDYMENT FARMS INC recalls Fiddyment Farms Fiddy Fire In-Shell Pistachios 2.5 oz., 8 oz., 1 lb., 2 lb., 3 lb., 5 lb., Fiddyment Farms Fiddy Fire
Fiddyment Farms recalls pistachios with undeclared hydrolyzed soy protein. Consumers should check product labels for UPCs 04283610003, 04283610008, 04283610016, 04283610048, 04283610080, 04283610025, 04283610003. No remedy specified in recall notice.
Fiddyment FarmsApr 29, 2019 - Use cautionVehicle
MITSUBISHI MIRAGE G4 (2018) recall — Air Bags
Mitsubishi recalls 2017-2018 Mirage G4 vehicles with air bags that may not deploy during crashes due to sensor misinterpretation of vibrations.
MitsubishiApr 26, 2019 - Use cautionVehicle
FORD TRANSIT (2018) recall — Seats
FORD TRANSIT 2018 models with Fenton Mobility Freedman GO-ES Foldaway Seats may move during crashes, increasing injury risk. Owners must contact Fenton Mobility for free seat repair by June 2019.
Fenton MobilityApr 26, 2019 - Use cautionMedical device
Cook Inc. recalls Zenith Alpha Abdominal Endovascular Graft, Reference Part Numbers: ZIMB-22-108, ZIMB-22-118, ZIMB-22-128, ZIMB-22-70,
Cook recalls Zenith Alpha Abdominal Endovascular Grafts with specific part numbers due to potential damaged gray safety lock knob that may cause deployment issues during surgery. Affected units may require medical intervention.
CookApr 26, 2019 - Use cautionMedical device
Inovo, Inc recalls Inovo Single Luman Conserver Product Usage: This device is intended to regulate the flow of oxygen from an oxygen tank
Inovo recalls Single Luman Conserver oxygen regulators with serial numbers starting with C0019802 to C0020216. The pressure gauge may dislodge from the threaded mount, creating an oxygen leak. Users should stop using the device immediately.
InovoApr 26, 2019 - Lower riskMedical device
Cytocell Ltd. recalls Aquarius D13S319 Plus Deletion Probe, Model LPH068-A Product Usage: The D13S319 probe, labelled in red, covers a 156kb
Cytocell recalls Aquarius D13S319 Plus Deletion Probe (Model LPH068-A) due to an error in the chromomap on the package insert. Affected units include specific lot numbers.
CytocellApr 26, 2019 - Lower riskMedical device
Exactech, Inc. recalls Opteform Allograft Disc, 30mm 3mm, 2cc, Catalog Number 600-03-30
Exactech recalls Opteform Allograft Discs (30mm, 45mm, 90mm) due to potential cold storage equipment failure causing higher temperatures than specified. Affected units have specific catalog and serial numbers.
ExactechApr 26, 2019 - Lower riskMedical device
Terumo Medical Corporation recalls SOLOPATH Balloon Expandable TransFemoral System, Model Numbers STFI-1425, STFI-1435, STFI-1625, STFI-1635, STFI-1825,
Terumo recalls SOLOPATH Balloon Expandable TransFemoral Systems (models STFI-1425 to STFI-2135) due to potential tip dislodgement from the sheath, which could cause loss of smooth transition during vascular procedures.
TerumoApr 26, 2019 - Stop using nowMedical device
PF Consumer Healthcare 1 LLC recalls ThermaCare HEATWRAPS, ADVANCED BACK PAIN THERAPY, UPC 305733010037 - Product Usage: ThermaCare(R) HeatWraps are
ThermaCare recalls heat wraps with lot S97473 due to potential overheating causing skin burns. Affected units may cause blisters or irritation. Stop using immediately.
ThermaCareApr 26, 2019 - Lower riskDrug
Advanced Pharma Inc. recalls HYDROmorphone 20 mg/100 mL Injectable Solution, Hydromorphone HCl 20 mg 0.9% Sodium Chloride 100 mL, Sterile single use
Advanced Pharma recalls hydromorphone 20 mg/100 mL injectable solution with sub-potency risk. This may not provide intended pain relief. Consumers should contact the manufacturer for details.
Advanced PharmaApr 26, 2019 - Lower riskFood
Dangonds Foods LLC recalls Dangonds Arepas de Queso, Net Weight 1,400g
Dangonds Foods LLC recalls Arepas de Queso (1,400g) due to missing milk allergen label. This poses a risk for people with milk allergies. Consumers should check lot numbers and contact the company for details.
DangondsApr 26, 2019 - Lower riskFood
Oregons Wild Harvest Inc recalls Dried whole elderberry, Oregon s Wild Harvest brand, packaged in metalized plastic bag, net wt. 4 oz or 1 lb. Each case
Oregon s Wild Harvest recalls dried whole elderberries due to glass fragments contamination. Products sold in metalized plastic bags, 4 oz or 1 lb, may cause injury if consumed.
Oregon s Wild HarvestApr 26, 2019 - Stop using nowConsumer product
Kids II Recalls All Rocking Sleepers Due to Reports of Deaths
All Kids II Rocking Sleepers models recalled due to infant fatalities from rolling from back to stomach while unrestrained. Consumers must stop using and get refund/voucher.
Kids IIApr 26, 2019 - Use cautionVehicle
MAZDA MAZDA6 (2013) recall — Structure
Mazda recalls 2013 Mazda6 vehicles with potential corrosion weakening steering alignment. Owners must have cross member inspected by dealer for free repair to prevent crash risk.
MazdaApr 25, 2019 - Use cautionVehicle
JAGUAR F-TYPE (2015) recall — Air Bags
Jaguar recalls 2014-2015 F-Type vehicles with potential front air bag deployment for children in front seat during crashes, increasing injury risk. Owners must have seat belt harness inspected and repaired free by dealers.
JaguarApr 25, 2019 - Use cautionVehicle
RAM 1500 (2019) recall — Power Train
Chrysler is recalling 2018-2019 RAM 1500 trucks with a potential driveshaft fracture risk. This could cause loss of drive power or increase crash risk. Owners must contact FCA US for free replacement.
RAMApr 25, 2019 - Use cautionVehicle
CHEVROLET SILVERADO 2500 (2019) recall — Engine
GM recalls 2019 Silverado 2500/3500 and 2017-2019 Silverado 2500/3500 with Duramax diesel engines for short circuit fire risk. Free engine block heater replacement.
ChevroletApr 25, 2019 - Use cautionMedical device
Medline Industries Inc recalls Endoscopic Cleaning Brushes sold in various Endoscopy Kits - Product Usage: The brushes are used to help clean out the
Medline recalls endoscopic cleaning brushes sold in specific kits due to potential brush detachment during cleaning, which could leave brush inside scope. Affected kits and lots listed.
MedlineApr 25, 2019 - Lower riskMedical device
The Binding Site Group, Ltd. recalls C-Reactive Protein Kit for use on the SPAplus, REF NK044.S.A, Rx only, UDI (01)05051700018456,
The Binding Site recalls C-Reactive Protein kits for SPAplus devices due to potential inaccurate test results for low concentrations. Affected kits may not detect samples below 10 mg/L correctly.
The Binding SiteApr 25, 2019 - UnratedMedical device
ASTRA, LLC recalls Lidar System for Erosion Flume Application Class 1 Laser Product Product Usage: Product is installed and fixed above a
ASTRA recalls Lidar System for Erosion Fl: Class 1 laser product with incorrect labeling may cause safety risks in indoor flume applications. Affected units installed above water erosion flumes.
ASTRAApr 25, 2019
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