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
35,004 found- Lower riskFood
Taylor Farms New England, Inc. recalls Hannaford brand Grilled Salmon meal with cooked brown rice, quinoa blend, broccoli florets, cooked white rice, fire
Taylor Farms recalls Hannaford brand Grilled Salmon meal with undeclared wheat. Consumers should check product labels for wheat ingredients and avoid if allergic.
Taylor FarmsDec 16, 2019 - Stop using nowFood
MUNK PACK INC recalls Munk Pack Peanut Butter Dark Chocolate Nut & Seed Bar, 35 g, individual unit
Munk Pack recalls 35g Peanut Butter Dark Chocolate Nut & Seed Bars due to undeclared milk. Check your UPC and expiration date.
Munk PackDec 16, 2019 - Stop using nowFood
Bakkavor Foods USA Inc. recalls HOME CHEF HEAT & EAT Baked Macaroni & Cheese NET WT. 12 oz (340G) keep refrigerated, Distributed by: The Kroger Co.,
Home Chef Heat & Eat Baked Macaroni & Cheese (12 oz) is recalled due to black plastic pieces. Check your fridge and UPC.
Home ChefDec 14, 2019 - Stop using nowMeat & poultry
FSIS Issues Public Health Alert for Chicken Soup due to Misbranding and an Undeclared Allergen
H-E-B Meal Simple Butter Chicken Soup (16-oz) is recalled due to undeclared wheat and soy. Do not consume; return or discard immediately.
H-E-B / Canyon Creek Soup Co.Dec 13, 2019 - Use cautionVehicle
FOREST RIVER GEORGETOWN (2020) recall — Trailer Hitches
Forest River recalls 2020 Georgetown motorhomes due to potential hitch detachment while towing, increasing crash risk. Owners must have bolts properly torqued by dealers.
Forest RiverDec 13, 2019 - Lower riskMedical device
Beckman Coulter Inc. recalls Beckman Coulter MicroScan PROMPT Inoculation System-D, Catalog Number B1026-10D, UDI: 15099590659561 - Product Usage:
Beckman Coulter recalls MicroScan PROMPT Inoculation System-D with incorrect wands that may cause false test results. Affected units have catalog number B1026-10D and UDI 15099590659561. Contact for remedy.
Beckman CoulterDec 13, 2019 - Lower riskMedical device
Randox Laboratories Ltd. recalls Liquid Clinical Chemistry Control, Catalogue Number: LAE4217, Size: 12 x 5 ml
Randox recalls Liquid Clinical Chemistry Control (LAE4217) due to incorrect lipase value in specific lot. This may affect lab test accuracy. No action needed for most users.
RandoxDec 13, 2019 - Lower riskMedical device
CooperSurgical, Inc. recalls ADVANCED ENDOSEE System CANNULA, Cooper Surgical Product Code/Model Number: ESPX5 The Advanced Endosee Cannula
Cooper Surgical recalls Endosee Cannula (ESPX5) with potential unsealed pouches in two lots. Affected units may have pouches that could leak, causing contamination. Stop using and contact for replacement.
Cooper SurgicalDec 13, 2019 - Stop using nowMedical device
TELEFLEX MEDICAL INC recalls HUDSON RCI COMFORT FLO Humidification System, REF 2410, humidifier nebulizer kit
Teleflex Medical recalls the HUDSON RCI Comfort Flo Humidification System (REF 2410) due to potential water flooding in the circuit during high-flow oxygen therapy.
Teleflex MedicalDec 13, 2019 - Lower riskDrug
The Harvard Drug Group recalls Memantine Hydrochloride Extended-release Capsules, 28mg, packaged in 100-count Unit Dose Cartons , Rx only,
The Harvard Drug Group recalls 28mg Memantine Hydrochloride Extended-release Capsules due to failed dissolution specifications observed in stability studies. This may affect medication effectiveness.
The Harvard Drug GroupDec 13, 2019 - UnratedDrug
Lupin Pharmaceuticals Inc. recalls Bimatoprost Ophthalmic Solution, 0.03%, For Use in the Eyes Only, Sterile, Rx Only, 7.5 mL bottle, Manufactured by:
Lupin Pharmaceuticals recalls 0.03% bimatoprost eye drops due to impurities in the solution. This medication is for prescription use only and may pose risks if impurities are present.
LupinDec 13, 2019 - UnratedDrug
Granules India Limited recalls RANITIDINE TABLETS, USP 150mg, 10,000-count bag, Country of Origin: INDIA NDC 62207-773-32
Granules India Limited recalls 150mg RANITIDINE tablets due to N-nitrosodimethylamine (NDMA) impurity found in the manufacturing process. This impurity may pose health risks with long-term use.
Granules India LimitedDec 13, 2019 - Lower riskFood
UNFI General Corporate recalls Essential Everyday, Unbleached Flour, Enriched All-Purpose Pre-Sifted, packaged in a 5lb paper bag
UNFI recalls 5lb paper bags of Essential Everyday Unbleached Flour due to Salmonella contamination. Consumers should check lot codes and contact UNFI for instructions.
UNFIDec 13, 2019 - Lower riskFood
Wayfare Health Foods LLC recalls Plant Based WayFare Butterscotch Pudding Organic Dairy Free, Item #1223. Net wt. 4 oz. There are 4/4 oz. cups per pack
Wayfare Health Foods recalls organic dairy-free butterscotch pudding due to bloating, sourness, and texture issues in some packages. Consumers should check lot numbers and return affected items.
WayfareDec 13, 2019 - Use cautionVehicle
RAM 1500 (2019) recall — Tires
Chrysler recalls 2019 Ram 1500 trucks with faulty TPMS sensors that don't warn of low tire pressure, increasing crash risk. Owners must get free sensor replacement.
ChryslerDec 12, 2019 - Use cautionVehicle
CHRYSLER PACIFICA (2019) recall — Back Over Prevention
Chrysler is recalling certain 2018-2019 Pacifica vehicles with 8.4-inch radios and 360-degree cameras. A software error causes rearview camera images to stay on after shifting out of reverse, potentially distracting drivers and increasing crash risk. Owners will receive free software updates.
ChryslerDec 12, 2019 - Use cautionVehicle
CADILLAC CT6 (2019) recall — Service Brakes, Hydraulic
General Motors recalls 2019 Cadillac CT6 vehicles with potential brake system failure. If ESC and ABS systems malfunction, drivers may not be aware, increasing crash risk. Free reprogramming available.
CadillacDec 12, 2019 - Use cautionVehicle
CHEVROLET SILVERADO 1500 (2020) recall — Electrical System
General Motors recalls 2019-2020 Chevrolet Silverado 1500 trucks with potential electrical issues causing stalling and fire risk. Owners must have dealer inspect for glue contamination at B+ cable connection.
ChevroletDec 12, 2019 - Use cautionMedical device
ResMed Ltd. recalls ResMed Stellar, Non-invasive/invasive ventilators, Model: 100, 150
ResMed recalls Stellar ventilators (Models 100/150) with serial numbers 20160123307-22171057208 due to potential alarm failure if stored without AC power for over 36 hours.
ResMedDec 12, 2019 - Lower riskMedical device
Arrow International Inc recalls Arrow Arterial Catherization Kit-20 Ga. x 4.45 cm Radiopaque Polyurethane over 22 Ga. TW Introducer Needle with
Arrow recalls arterial catheter kits with incorrect MRI safety labeling. The kit may be unsafe for MRI scans due to mislabeled magnetic resonance compatibility.
ArrowDec 12, 2019 - Use cautionMedical device
Baxter Healthcare Corporation recalls Clearlink System Continu-Flo Administration Sets, Product Codes: 2C8519, 2C8537, and 2C8541 - Product Usage:For the
Baxter recalls Clearlink Continu-Flo Administration Sets with specific product codes due to potential connection issues that may cause dislodgement during fluid administration.
BaxterDec 12, 2019 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Coonrad/Morrey Total Elbow Humeral Assembly, Extra Small, 4-inch Length. Model No. 32-8105-027-04. UDI
Zimmer Biomet recalls Coonrad/Morrey Total Elbow Humeral Assembly model 32-8105-027-04 due to two outer pins instead of one inner and one outer pin, which may cause improper joint function.
Zimmer BiometDec 12, 2019 - Use cautionVehicle
LINCOLN MKX (2017) recall — Electrical System
Ford is recalling 2016-2017 Lincoln MKX vehicles with 3.7L engines due to a risk of fire from electrical short circuits. Owners will receive free repairs by April 2020.
FordDec 11, 2019 - Use cautionVehicle
FORD F-250 SD (2019) recall — Exterior Lighting
Ford is recalling 2019 F-250 trucks with daytime running lights that may not dim, potentially reducing visibility and increasing crash risk. Owners must contact Ford for free software update.
FordDec 11, 2019 - Use cautionVehicle
FORD F-150 (2020) recall — Electrical System
Ford recalls certain 2019-2020 F-150s due to potential electrical issues causing engine stalls, reduced braking, or fire risks. Owners must have a dealer inspect the battery cable joint.
FordDec 11, 2019 - Lower riskMedical device
Lumitex Inc recalls Giraffe Blue Spot PT LiteTM Phototherapy System, Model Numbers M1224917, M1231533, M1225025, M1224961, M1224958,
Lumitex recalls specific models of Giraffe Blue Spot PT Lite phototherapy systems built between 2014-2018 due to potential light output falling below safe levels from heat exposure.
LumitexDec 11, 2019 - Use cautionMedical device
Suntech Medical, Inc. recalls Model 250D Ambulatory Blood Pressure Monitor labeled under the following brands: Bravo Mini, part number 99-0233-00;
Suntech Medical recalls Bravo Mini blood pressure monitors with model 250D due to battery misuse risks. Affected units may cause injury if rechargeable batteries are improperly handled.
Suntech MedicalDec 11, 2019 - Lower riskMedical device
Brasseler USA I Lp recalls Brasseler USA KM169-39-76 Steinmann Pin Single Diamond Smooth, Diameter 2.8 mm, Length 228 mm Product Usage: A
Brasseler USA recalls 103 tubes of Steinmann pins labeled incorrectly as KM169-39-76 instead of KM168-39-76. This labeling error may cause confusion in medical use. Affected units were sold with lot number NR8ZR.
Brasseler USADec 11, 2019 - Lower riskMedical device
Abaxis Inc recalls Piccolo Xpress chemistry analyzer, Model No. 1100-1001, Software version 2.1.55 (NGA)/3.1.35(Jen II)
Abaxis recalls Piccolo Xpress chemistry analyzers with specific model numbers and software versions due to incorrect reference ranges for analytes. Affected units may provide inaccurate test results.
AbaxisDec 11, 2019 - Lower riskMedical device
Centurion Medical Products Corporation recalls Centurion- Umbilical Trays UVT1045 UMBILICAL ARTERY TRAY UVT1055 UVC KIT UVT1065 UMBILICAL VESSEL CATHETER TRAY UVT170
Centurion Medical Products recalls umbilical trays due to incomplete sterile seals that may compromise sterility. Affected models include UVT1045, UVT1055, UVT1065, UVT170, UVT280, UVT460, UVT505, UVT630, UVT640, UVT665, UVT730, UVT795, UVT960A, and UVT970 with specific lot numbers. Consumers should stop using these items to prevent infection risks.
CenturionDec 11, 2019
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83,592 recalls tracked · 72,039 explained in plain English · 10,976 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.