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
34,956 found- Use cautionMedical device
Philips Electronics North America Corp. recalls Philips HeartStart FR3 Defibrillator, Model: 861388, 861389 Product Usage: The HeartStart FR3 is used to treat
Philips recalls two models of HeartStart FR3 defibrillators (serials starting with C17B, C17A, C16K, C16J) due to potential water damage causing device failure during use.
PhilipsOct 10, 2018 - Lower riskMedical device
Philips Electronics North America Corporation recalls IntelliVue MX40 Patient Monitor, Model Nos. 865350, 865351, 865352, 867146 - Product Usage: Indicated for use by health
Philips recalls IntelliVue MX40 patient monitors with specific model numbers due to potential speaker issues at high altitudes. Affected units may have inaudible audio above 4,500 feet in Monitor Mode, but no immediate action is required.
PhilipsOct 10, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Orthopedic Salvage System (OSS) Porous Stem, Item No. 150394
Zimmer Biomet recalls specific Orthopedic Salvage System (OSS) porous stems due to potential surgery extension risk if replacement parts are unavailable. Affected patients should contact the company for details.
Zimmer BiometOct 10, 2018 - Use cautionMedical device
Baxter Healthcare Corporation recalls L5C4531 X1 Integrated APD Set with Cassette 3-Prong Sterile, nonpyrogenic fluid path. Sterilized by ethylene oxide.
Baxter Healthcare recalls L5C453: X1 Integrated APD Sets with 3-prong cassettes due to potential leaks causing contamination and peritonitis risk. Affected units include specific lot numbers.
Baxter HealthcareOct 10, 2018 - Lower riskFood
Taylor Farms Pacific Inc. (MacArthur Facility) recalls Raley's Country Macaroni Salad labeled as Raley's Country Potato Salad; 32 oz. (907g) clear plastic containers; UPC
Taylor Farms recalls Raley's Country Macaroni Salad labeled as Potato Salad due to missing wheat allergen declaration. Consumers should check labels for correct product name and ingredients.
Taylor FarmsOct 10, 2018 - Stop using nowFood
SLR FOOD Distribution, Inc. recalls SUGAR MELON CANDY / WAX GOURD The product comes in a 7.04oz plastics package marked with barcode 6912567116718.
SLR Food Distribution recalls Sugar Melon Candy due to undeclared sulfites. Check your barcode and expiration date for details.
SLR Food DistributionOct 10, 2018 - Use cautionFood
The Kroger Co recalls simple truth organic Red Quinoa Ingredients: organic red quinoa Distributed by The Kroger Co, Cincinnati, OH
The Kroger Co is recalling Simple Truth Organic Red Quinoa because it tested not in compliance for pesticide exclusion. Check your Best By dates.
Simple Truth OrganicOct 10, 2018 - Stop using nowFood
Fine Land Corp recalls Meiqili Durian Candy in plastic bag with clear window, Net Wt: 12 ounce (340 g). It is a labeled as a product of P.R.C.
Fine Land Corp recalls Meiqili Durian Candy due to undeclared milk. Check your plastic bag with clear window for UPC 4-897055-795465-0.
MeiqiliOct 10, 2018 - Lower riskFood
Quest Nutrition, LLC recalls Quest Protein Bar Vanilla Almond Crunch Single Bar UPC# - 888849000494 12 ct. Box UPC # - 888849000500
Quest Nutrition recalls Vanilla Almond Crunch protein bars due to undeclared tree nut (almond) allergen. Consumers should check UPCs 888849000494 and 888849000500 for affected products.
QuestOct 10, 2018 - Lower riskFood
P. East Trading Corp. recalls Fruits Du Sud brand Golden Seedless Raisins packed in 30 Lb. boxes with Lot No. FDS T499/18 and Production date of
P. East Trading Corp. recalls Fruits Du Sud Golden Seedless Raisins (30 lb boxes, Lot FDS T499/18, April 2018) due to undeclared sulfites. Consumers should check labels and contact the company for details.
Fruits Du SudOct 10, 2018 - Use cautionConsumer product
Spiraledge Recalls Yoga Backless Chairs Due to Fall Hazard (Recall Alert)
Spiraledge recalls yoga chairs that can break at the seat or back support, causing falls. Consumers must stop using and get a refund via store gift card.
SpiraledgeOct 10, 2018 - Stop using nowConsumer product
Canyon Recalls Mountain Bikes Due to Crash Hazard (Recall Alert)
Canyon recalls 2018 Spectral mountain bikes with aluminum chainstays that can crack, leading to rear wheel detachment and crashes. Affected models include M71 Spectral CF 9.0 PRO and others. Consumers must stop using and return for free chainstay replacement.
CanyonOct 10, 2018 - Stop using nowConsumer product
Briggs & Stratton Recalls Portable Generator Fuel Tank Replacement Caps, Due to Fire Hazard
Briggs & Stratton recalls fuel tank replacement caps lacking ventilation holes, which can cause pressure buildup and fire. Stop using immediately.
Briggs & StrattonOct 10, 2018 - Use cautionVehicle
FORD C-MAX (2015) recall — Equipment
Ford is recalling 2013-2015 C-Max Energi and Fusion Energi vehicles with specific 120V convenience cords that can overheat and melt during charging, increasing fire risk. Owners must replace cords with new thermistor-equipped models.
FordOct 9, 2018 - Use cautionMedical device
Synaptive Medical Inc recalls BrightMatter Guide, Product Number SYN-0026, Versions: 1.5.0, 1.5.1 and 1.5.2 Product Usage: BrightMatter Guide can
Synaptive Medical recalls BrightMatter Guide software versions 1.5.0-1.5.2 due to a defect that may cause errors during surgical procedures when switching between blue and gold NICO BrainPath ports.
Synaptive MedicalOct 9, 2018 - Lower riskMedical device
Theragenics Corporation recalls Theragenics Applicator Needle (18g x 20cm) The device is comprised four basic elements; a wire stylus with plastic
Theragenics recalls 18g x 20cm Applicator Needles due to unsealed pouches that may cause contamination. Affected units sold with lot #180904-80.
TheragenicsOct 9, 2018 - UnratedMedical device
Fresenius Medical Care Renal Therapies Group, LLC recalls Fresenius Granuflo Dry Acid Concentrate- 2K 2.0 Ca 1 Mg 16.5 GAL Catalog Number: OFD2201-3B for hemodialysis
Fresenius recalls Granuflo Dry Acid Concentrate-2K 2.0 Ca 1 Mg 16.5 GAL (Lot 18ETGF005) due to discolored powder containing foreign substances. Affected hemodialysis patients should contact for remedy.
FreseniusOct 9, 2018 - Use cautionDrug
Lupin Pharmaceuticals Inc. recalls Testosterone Topical Solution, 30mg/1.5mL, 110mL bottles, Rx only, Manufactured for: Lupin Pharmaceuticals Inc.
Lupin Pharmaceuticals recalls specific lots of Testosterone Topical Solution because the pump may not work. Check your bottle's lot number and expiration date.
Lupin PharmaceuticalsOct 9, 2018 - Lower riskDrug
Sprayology recalls AllergEase, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC
Sprayology recalls AllergEase homeopathic oral spray due to potential microbial contamination from manufacturing issues. Consumers should check product details and contact the company for guidance.
SprayologyOct 9, 2018 - Lower riskFood
World Variety Produce Inc. recalls Melissa's Hatch Chile Clean Snax, with Chia and flaxseed; 6.5 oz. plastic clamshell tub. Ingredients: Peanuts, Almonds,
World Variety Produce recalls Melissa's Hatch Chile Clean Snax with chia and flaxseed for missing peanuts in allergen information, posing a risk for peanut allergies.
World Variety ProduceOct 9, 2018 - Stop using nowConsumer product
Marker Recalls Kingpin Ski Bindings Due to Fall Hazard
Recall of 2017-2018 Kingpin 10 and 13 ski bindings with black body and gold/copper accents due to risk of binding failure causing falls. Return to authorized retailer for free replacement toe unit.
MarkerOct 9, 2018 - Use cautionConsumer product
Cracker Barrel Old Country Store Recalls Decorative Pineapples Due to Laceration Hazard
Cracker Barrel recalls decorative driftwood pineapples with sharp metal leaves that can cause cuts. Return for full refund at any store or online.
Cracker Barrel Old Country StoreOct 9, 2018 - Use cautionVehicle
KZRV SPORTSMEN (2019) recall — Equipment
KZRV is recalling 2018-2019 Sportsmen 333BHK Trailers due to propane lines that may be damaged by road debris, increasing fire risk. Owners must have a steel plate installed free of charge.
KZRVOct 8, 2018 - Lower riskMedical device
Ortho-Clinical Diagnostics recalls VITROS¿ Chemistry Products dLDL Reagent-GENs 26 & 27. In Vitro Diagnostic to quantitatively measure LDL Cholesterol
Ortho-Clinical Diagnostics recalls VITROS dLDL Reagent GENs 26 & 27 due to potential negative results. Affected units have specific lot numbers and expiration dates. Contact for replacement.
Ortho-Clinical DiagnosticsOct 8, 2018 - Lower riskMedical device
bioMerieux, Inc. recalls bioM¿rieux NucliSENS easyMAG Lysis Buffer ref. 280134
Biomerieux recalls NucliSENS easyMAG Lysis Buffer (ref. 280134) due to potential colored eluates from residual hemoglobin. Affected units were sold with specific lot number and expiration date.
BiomerieuxOct 8, 2018 - Use cautionMedical device
Voluntis recalls Insulia Diabetes Management Companion
Voluntis recalls Insulia Diabetes Management app versions 1.4.3, 1.6.3, 1.6.31, and 1.6.40 due to a bug that could cause low-impact to high-impact hypoglycemia. Update to version 1.6.42 resolves the issue.
VoluntisOct 8, 2018 - Use cautionMedical device
Stryker Medical Division of Stryker Corporation recalls The Spirit Plus Bed, Model 5600 Spirit Plus /with high rail siderail option
Stryker recalls Spirit Plus Bed Model 5600 with high rail siderail option due to potential entrapment risk. Affected units have specific serial numbers listed in the recall notice.
StrykerOct 8, 2018 - Lower riskDrug
Akorn, Inc. recalls Gentamicin Sulfate Ophthalmic Solution, USP 0.3%, 5 mL dropper bottle, Rx Only, Manufactured by: Akorn, Inc. Lake
Akorn recalls Gentamicin Sulfate Ophthalmic Solution 0.3% 5mL bottles due to crystalline particles found at 24-month testing. This may cause eye injury if used.
AkornOct 8, 2018 - Lower riskDrug
ICU Medical Inc recalls 0.9% Sodium Chloride Injection, USP Rx Only a) 250 mL NDC 0409-7983-02; b) 150 mL NDC 0409-7983-61; c) 50 mL NDC
ICU Medical recalls 250mL, 150mL, and 50mL 0.9% Sodium Chloride injections due to potential leakage risks. These products may cause infections if not sterile.
ICU MedicalOct 8, 2018 - Use cautionFood
Forager Project LLC recalls Forager Project Organic Protein Plant Shake Nuts & Vanilla 12 fl oz. UPC: 8 14558 02038 6
Forager Project recalls organic protein plant shake with undeclared tree nuts (almonds) due to allergen risk. Consumers should check UPC 8 14558 02038 6 for affected products.
Forager ProjectOct 8, 2018
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