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
Jac Vandenberg Inc. recalls Peaches, sold as a bulk retail item, with PLU 4044, and country of origin of Chile. The peaches sold at Aldi are
Jac Vandenberg recalls peaches from Chile with PLU 4044 sold at Aldi, potentially contaminated with Listeria monocytogenes. Consumers should avoid eating these products.
Jac VandenbergJan 22, 2019 - Lower riskMedical device
Stryker GmbH recalls Instrument Tray, Basic T2 Femur Long Catalog #: 1806-9900 Product Usage: Knee Arthroplasty
Stryker recalls Basic T2 Femur Long Instrument Tray (lot K026ACE/KU97181) due to risk of using wrong instrument set during knee surgery. Affected users should verify model numbers.
StrykerJan 21, 2019 - Lower riskFood
Perrigo Company PLC recalls Simple Truth Organic Banana, Strawberry & Apple Fruit Puree with Nonfat Greek Yogurt, 113 g, packed in a laminate
Perrigo recalls Simple Truth Organic Banana, Strawberry & Apple Fruit Puree with Nonfat Greek Yogurt due to improper labeling that fails to indicate milk content. This affects one lot (L8159) with best by date 08/06/2019.
PerrigoJan 21, 2019 - Lower riskFood
PBM Nutritionals, LLC recalls Parent's Choice Toddler Next Stage¿ Milk Drink Powder Natural Milk Flavor With Other Natural Flavors, Stage 3, 1 Year
PBM Nutritionals recalls Parent's Choice Toddler Next Stage Milk Drink Powder (Stage 3) due to potential foreign material. Consumers should check lot codes T16DTKC, T17DTJC, or T20DTDC for affected products.
PBM NutritionalsJan 21, 2019 - Lower riskMedical device
GE Healthcare, LLC recalls Revolution CT scanners Product Usage: The system is intended for head, whole body, cardiac and vascular X-ray Computed
GE Healthcare recalls Revolution CT scanners due to potential additional low dose radiation exposure during medical imaging. Affected units may require special handling to minimize radiation risks.
GE HealthcareJan 19, 2019 - Use cautionMeat & poultry
Custom Made Meals, LLC Recalls Chicken Skewer Products Due to Misbranding and Undeclared Allergens
USDA FSIS recalls 7,954 pounds of Custom Made Meals chicken skewers containing undeclared coconut, a tree nut allergen. Consumers urged not to consume or discard products.
Custom Made MealsJan 18, 2019 - Lower riskMeat & poultry
H & T Seafood, Inc. Recalls Siluriformes Products Produced without Benefit of Import Inspection
H & T Seafood recalls 71,435 pounds of frozen siluriformes fish products imported from Vietnam that skipped U.S. import re-inspection. Consumers are urged not to eat these products.
H & T SeafoodJan 18, 2019 - Stop using nowMeat & poultry
Johnsonville, LLC Recalls Raw Ground Frozen Cheddar Cheese and Bacon Flavored Pork Patty Products Due to Possible Foreign Matter Contamination
Johnsonville recalls 48,371 pounds of frozen pork patties with possible black rubber contamination. Consumers are urged not to eat these products and should discard or return them.
JohnsonvilleJan 18, 2019 - Use cautionVehicle
HEARTLAND TRAIL RUNNER (2019) recall — Equipment
Heartland is recalling 2019 Trail Runner trailers with incorrect tire pressure labels that could increase crash risk. Owners should check for certification labels and contact customer service for free replacements.
HeartlandJan 18, 2019 - Lower riskMedical device
Bellus Medical recalls SKINFUSE Resuce Calming Complex Kit containing: SKINFUSE LIFT HG - Product Usage: The SKINFUSE Rescue Calming Complex
Bellus Medical recalls SKINFUSE Rescue Calming Complex Kit that contains a mislabeled medical product. This cosmetic kit includes a hydrogel wound dressing intended for microneedling procedures.
Bellus MedicalJan 18, 2019 - Use cautionDrug
Mylan Institutional, Inc. (d.b.a. UDL Laboratories) recalls Alprazolam Tablets, USP, 0.25 mg, 10x10 per carton, Rx Only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown,
Mylan recalls specific lots of Alprazolam Tablets, USP 0.25 mg due to elevated impurity levels. Check your NDC and expiration date.
MylanJan 18, 2019 - Lower riskDrug
Mylan Pharmaceuticals Inc. recalls Fexofenadine HCl Tablets, USP, 180 mg, packaged in a) 30-count bottles (NDC 0378-0782-93) and b) 500-count bottles (NDC
Mylan recalls 180mg fexofenadine tablets with slightly elevated impurities from stability testing. Consumers should check NDC codes and expiration dates for affected lots.
MylanJan 18, 2019 - Lower riskDrug
Prinston Pharmaceutical Inc recalls Irbesartan and Hydrochlorothiazide Tablets, USP 300/12.5 mg Rx Only Manufactured by: Zhejiang Huahai Pharmaceutical
Prinston Pharmaceutical recalls 30-count Irbesartan/Hydrochlorothiazide tablets (NDC 43547-331-03) due to FDA-confirmed NDEA impurity exceeding safe levels. Consumers should contact Solco Healthcare for details.
Prinston PharmaceuticalJan 18, 2019 - Lower riskFood
Mrs Grissom's Salads, Inc recalls Mrs GRISSOM'S SELECT OLD FASHIONED PIMENTO CHEESE**Mrs. GRISSOM'S SELECT CRANBERRY PECAN CHICKEN SALAD**INGREDIENTS:
Mrs Grissom's Select Old Fashioned Pimento Cheese and Cranberry Pecan Chicken Salad contain undeclared milk allergen. Consumers should check labels for egg, soy, and pecans.
Mrs Grissom'sJan 18, 2019 - Use cautionMeat & poultry
Perdue Foods LLC Recalls Simplysmart Organics Gluten Free Chicken Nugget Products Due to Possible Foreign Matter Contamination
Perdue Foods recalls gluten-free chicken nuggets from 2018 due to possible wood contamination. Consumers are urged not to eat these products and should discard or return them.
PerdueJan 17, 2019 - Use cautionVehicle
WINNEBAGO ERA (2017) recall — Equipment
Winnebago is recalling 2012-2018 ERA motorhomes due to risk of cabinet shelf detachment causing distraction or injury to drivers. Owners must contact Winnebago for free safety fixes.
WinnebagoJan 17, 2019 - Use cautionVehicle
LAND ROVER RANGE ROVER (2019) recall — Engine
Land Rover is recalling 2019 Range Rover vehicles with V6/V8 engines due to crankshaft pulley retaining bolt fracture risk causing engine failure and potential crash.
Land RoverJan 17, 2019 - Use cautionVehicle
JAGUAR F-TYPE (2019) recall — Engine And Engine Cooling
Jaguar recalls 2019 F-Type vehicles with V6/V8 engines due to crankshaft pulley bolt fracture risk causing engine failure. Owners must contact dealers for free replacement.
JaguarJan 17, 2019 - Use cautionVehicle
HEARTLAND TRAIL RUNNER (2019) recall — Tires
Heartland is recalling 2019 Trail Runner trailers with Load Range D tires that may fail, increasing crash risk. Owners can get free replacement tires from dealers.
HeartlandJan 17, 2019 - Lower riskMedical device
CryoLife, Inc. recalls On-X Aortic Heart Valve with Anatomic Sewing Ring Product Usage: The On-X Prosthetic Heart Valve is indicated for the
CryoLife recalls On-X Aortic Heart Valve with incorrect serial number labeling. Affected units have model ONXANE-23, lot 6827216. No immediate action needed as mislabeling does not affect safety.
CryoLifeJan 17, 2019 - Lower riskMedical device
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls MEDTRONIC CARELINK 2090 programmer
Medtronic is recalling CareLink 2090 programmers with specific serial numbers due to an error in calculating and displaying the remaining time before the device should be replaced. This could cause users to replace their device too early or too late. Affected units include those with serial numbers listed in the recall notice.
MedtronicJan 17, 2019 - Lower riskMedical device
DJO, LLC recalls Aircast REF 3011 - PL RX only VF-PL Sterile Cuff Pkg., Lot# 418003, Expiration Date: 2020 -12 - 31, Made in Mexico,
DJO recalls Aircast REF 3011 sterile cuff packages (Lot #418003) due to potential failure to meet sterility standards. This affects medical use items sold through specific channels.
DJOJan 17, 2019 - Use cautionMedical device
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls Medtronic Power Supply 26907, Medtronic CareLink Encore(TM) 29901 Programmer
Recall of Medtronic Power Supply 26907 and CareLink Encore 29901 Programmer due to potential electrical short circuits causing overheating, smoke, and disconnection. Affected units have specific serial numbers.
MedtronicJan 17, 2019 - Lower riskMedical device
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls Medtronic implantable pulse generator: RELIA, Dual chamber pacemaker (VDD): (a) Model Number RED01 (b) Model Number
Medtronic recalls specific dual chamber pacemaker models (RED01, REDR01, REVDD01) distributed 2017-2019 that may experience circuit errors affecting device function. Owners should contact Medtronic for details.
MedtronicJan 17, 2019 - Lower riskFood
Friendly Fruit Market dba Sid Wainer & Son recalls JANSAL VALLEY Cocoa Dusted Chocolate Covered Almonds, Net Weight: 6 OZ (170 G), packed in a plastic clamshell, UPC: 7
Friendly Fruit Market recalls 6oz cocoa-dusted chocolate covered almonds due to undeclared sesame seeds. Consumers should check UPC 708152329887 for affected lots.
Friendly Fruit MarketJan 17, 2019 - UnratedFood
ProThera, Inc. dba SFI USA recalls Klaire Labs Melatonin Lozenge Formula Fast Dissolving 1 mg tablets; Packed in a 75 cc HDPE Bottle 60 Tablets UPC: 8
SFI USA recalls melatonin loz: Klaire Labs 1mg fast dissolving tablets with L-Theanine contamination. No remedy provided in official notice.
SFI USAJan 17, 2019 - Stop using nowVehicle
CHEVROLET MALIBU (2011) recall — Air Bags
General Motors recalls 2011 Chevrolet Malibu vehicles with potential air bag inflator explosion causing serious injury or death during deployment.
ChevroletJan 16, 2019 - Use cautionVehicle
AUDI Q7 (2018) recall — Fuel System, Gasoline
Audi is recalling 2018 Q7 vehicles with a potential fuel leak that could cause fire if near ignition sources. Owners must have fuel rails replaced free by dealers.
AudiJan 16, 2019 - Use cautionVehicle
KYMCO LIKE 150I (2019) recall — Fuel System, Gasoline
KYMCO is recalling 2018-2019 Like 150i motorcycles with a fuel pump leak risk that could cause fire. Owners must get free fuel pump replacement.
KYMCOJan 16, 2019 - Lower riskMedical device
Intuitive Surgical, Inc. recalls daVinci Harmonic ACE Curved Shears
Intuitive Surgical recalls daVinci Harmonic ACE Curved Shears due to potential sterility breaches from damaged packaging during transit. Affected units may have pinholes or small openings in sterile pouches.
Intuitive SurgicalJan 16, 2019
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