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
34,893 found- Lower riskFood
J F C International Inc recalls Futaba Sesame Hijiki Rice Seasoning; 2.29 oz. glass jar; 4 902533 023173
J F C International recalls Futaba Sesame Hijiki Rice Seasoning jars from June 2016-2017 due to missing English labels and unlisted allergens like wheat, soybean, and fish.
J F C InternationalJun 20, 2017 - Stop using nowFood
Penobscot McCrum LLC recalls Battered Jo-Jo Wedges / 00047 (5 lb bags)
Penobscot McCrum LLC recalls 5 lb bags of Battered Jo-Jo Wedges due to undeclared milk. Check your lot codes immediately.
Jo-JoJun 20, 2017 - Stop using nowConsumer product
Staples Recalls Hazen Mesh Office Chairs Due to Fall Hazard
Staples recalls Hazen Mesh Task chairs with a fall hazard due to potential base leg breakage. Affected chairs have SKU 10582:26680. Consumers must stop using and get a free replacement base.
StaplesJun 20, 2017 - Stop using nowConsumer product
Kawasaki Recalls Utility Vehicles, Recreational Off-Highway Vehicles and All-Terrain Vehicles Due to Fire Hazard (Recall Alert)
Kawasaki recalls 2017 Mule, Teryx and Brute Force 750 vehicles due to fuel gauge retainer collapse causing fire risk. Owners must stop using immediately and contact for free repair.
KawasakiJun 20, 2017 - Lower riskMedical device
Nova Biomedical Corporation recalls Nova Biomedical Stat Profile Prime Analyzer as follows: PN 52855 Stat Profile Prime ABG Analyzer PN 53655 Stat Profile
Nova Biomedical recalls Stat Profile Prime analyzers with specific model numbers due to software that may overwrite patient results before they are released. Affected units include PN 52855, 52856, 528:53655, 53656, 53657, 52857. No remedy is specified in the recall notice.
Nova BiomedicalJun 19, 2017 - Lower riskMedical device
Elekta, Inc. recalls iGUIDE Software 2.2 Product Usage: Control of accurate patient positioning with assistance of a 30 Tracking System in a
Elekta recalls iGUIDE Software 2.2 versions due to incorrect PEC values that could affect patient positioning accuracy in radiotherapy. Affected units include iGUIDE 2.2.0 and 2.2.1.
ElektaJun 19, 2017 - Lower riskMedical device
Leica Microsystems, Inc. recalls Nussloch GmbH ASP6025 Tissue Processor
Leica Microsystems recalls ASP6025 Tissue Processors with specific serial numbers due to incorrect voltage labeling on alarm connectors, which could lead to improper operation.
LeicaJun 19, 2017 - Lower riskMedical device
ConMed Corporation recalls STAT 2¿ I.V. Gravity Flow Controller and STAT 2¿ Primary, Secondary Administration Sets and Extension Sets (Catalog
ConMed recalls STAT 2.5 I.V. gravity flow controllers and administration sets due to inconsistent fluid flow rates. Affected units include specific catalog numbers and production dates from April 2012 to February 2017.
ConMedJun 19, 2017 - Lower riskDrug
Fagron Compounding Services LLC dba Fagron Sterile Services recalls Succinylcholine Chloride, 100 mg per 5mL, 20 mg per mL syringe. IV Use Only. JCB Laboratories, 8710 E 34th St., N.
Fagron Sterile Services recalls specific Succinylcholine Chloride syringes (IV use only) due to lack of sterility assurance. This voluntary recall was initiated by the manufacturer to prevent potential infections.
Fagron Sterile ServicesJun 19, 2017 - Lower riskDrug
Apace KY LLC recalls Amantadine HCl Capsules, USP, 100 mg, Rx Only, 50 Capsules (5x10) Unit Dose Cartons, Manufactured for: AvKARE Inc,
Apace KY LLC recalls 50-capsule amantadine HCl units sold in TN with cyclobenzaprine tablets inside. Label mix-up risks incorrect medication use.
Apace KYJun 19, 2017 - Lower riskMeat & poultry
Supreme Cuisine Recalls Meat and Poultry Fat and Lard Products Due to Processing Deviation
USDA FSIS recalls 325,000 pounds of Supreme Cuisine meat and poultry fat products due to a processing deviation that may allow bacterial pathogens to grow.
Supreme CuisineJun 17, 2017 - UnratedFood
House Of Thaller Inc recalls Marketside CLASSIC HUMMUS WITH PINE NUTS NET WT. 10 oz (283g)
House Of Thaller recalls Marketside Classic Hummus with Pine Nuts due to potential Listeria monocytogenes contamination. Consumers should check expiration dates and lot codes on the product.
House Of ThallerJun 17, 2017 - Use cautionMeat & poultry
Channel Fish Processing Co., Inc. Recalls Siluriformes Fish Products Due to Misbranding and Undeclared Allergens
USDA FSIS recalls 840 lbs of breaded Swai fillets for undeclared milk allergen. Consumers urged not to consume; products should be thrown away or returned.
Channel Fish ProcessingJun 16, 2017 - Lower riskMeat & poultry
Embutidos Fanguito, Inc. Recalls Pork Products Due to Mislabeling, Misbranding, and Undeclared Allergens
USDA FSIS recalls pork products from Embutidos Fanguito due to mislabeling as cooked, undeclared soy and MSG allergens. Consumers urged not to consume these products.
Embutidos FanguitoJun 16, 2017 - Lower riskMedical device
Zimmer Biomet, Inc. recalls ExploR Radial Head Replacement System. PN: 11-210061 LN: 243610. The stem is placed inside a polyurethane bag. The
Zimmer Biomet recalls ExploR 6x24mm Implantable Stem with Screw due to missing modular radial HD lock screw in package. Consumers should check if their product has the lot number 243610 or 202900.
Zimmer BiometJun 16, 2017 - Stop using nowMedical device
Maquet Datascope Corp - Cardiac Assist Division recalls CS 300 Intra-Aortic Balloon Pump
Maquet Datascope recalls CS 300 Intra-Aortic Balloon Pumps that failed to pump due to electrical test failures, linked to patient deaths. Affected units have specific model numbers.
Maquet DatascopeJun 16, 2017 - Lower riskMedical device
Keystone Dental Inc recalls Max Implant System - Bone Tap for use with 7.0mm diameter Max Implant, Catalog Number D-TAP-MAX7-7 Dental implants are
Keystone Dental recalls Bone Tap (Catalog D-TAP-MAX7-7) that was laser marked 8mm but labeled 7mm. This mismatch risks improper implant fitting. Affected units sold with specific catalog and lot numbers.
Keystone DentalJun 16, 2017 - Lower riskDrug
Sandoz Incorporated recalls Amitriptyline HCl Tablets, USP 25 mg, Packaged in a)100-count bottles (NDC 0781-1487-01) and b) 1000-count bottles (
Sandoz recalls 25mg Amitriptyline HCl tablets due to cross contamination with imipramine. Affected lots expire August 2019. Consumers should contact Sandoz for details.
SandozJun 16, 2017 - Stop using nowDrug
Alvogen, Inc recalls Clindamycin Injection USP; 600 mg/4 mL (150 mg/mL). 4 mL Single-dose ADD-VANTAGE Vial, Rx Only, Manufactured for
Alvogen recalls 4mL single-dose clindam: Risk of contamination from lack of sterility assurance. Check NDC 47781-463-69 and lot numbers for affected vials.
AlvogenJun 16, 2017 - Lower riskDrug
Time-Cap Laboratories, Inc. recalls Ibuprofen Tablets, USP 600 mg, 500-count bottle (Capsule Shaped), Rx only, Manufactured for: Time Cap Labs, Inc., 7
Time Cap Labs recalls 500-count 600mg Ibuprofen tablets (Rx only) that contain some 800mg tablets. Consumers should check product details and contact the company for guidance.
Time Cap LabsJun 16, 2017 - Lower riskFood
Threshold Enterprises Ltd recalls Planetary Herbals Ginseng Classic; Classic Chinese Energizer 710 mg; 60 and 120 UPC 0 21078 10215 1 tablet bottles; 60
Planetary Herbals recalls two ginseng supplement products due to coliform bacteria contamination detected during testing. Consumers should check product codes and lot numbers for affected items.
Planetary HerbalsJun 16, 2017 - Stop using nowFood
New Hope Mills Mfg., Inc. recalls Cost Plus World Market My Favorite Macadamia Pancake and Waffle Mix, 24 oz. UPC Codes: 496960
Cost Plus World Market recalls 24 oz My Favorite Macadamia Pancake and Waffle Mix due to potential Listeria Monocytogenes contamination. Check your UPC.
Cost Plus World MarketJun 16, 2017 - Stop using nowFood
Unified Seafood Company., Inc. recalls Pacific Wave Frozen Tuna Loins; 30# case. Imported by Unified Seafood Co., Inc. www.unifiedseafood.com
Unified Seafood Co. recalls Pacific Wave frozen tuna loins after positive Hepatitis A test results. Check your freezer for affected lots and discard immediately.
Pacific WaveJun 16, 2017 - Lower riskFood
Hmshost recalls Cape Cod Cranberry Trail Mix; 25 lbs. bulk containers; cardboard box; expiration date 11/18/17.
Hmshost recalls 25-lb Cape Cod Cranberry Trail Mix with Listeria risk. Products expired 11/18/17. Consumers should check for lot #1716 and discard if expired.
HmshostJun 16, 2017 - Lower riskFood
Rikki USA, Inc. recalls Masas Gourmet Curry Coconut Sauce, packaged in a glass jar with gold metal cap, net wt. 12 oz. (355 mL), UPC
Masas Gourmet Curry Coconut Sauce with gold metal cap may not list milk in ingredients due to labeling error. Recalled lots from 2017-2018. No action needed per official notice.
MasasJun 16, 2017 - Use cautionConsumer product
Advanced Composites Recalls Bicycle Forks Due to Fall Hazard (Recall Alert)
Advanced Composites recalls select Wound Up Tandem Duo Disc bicycle forks (June 2015-Dec 2015) due to risk of fork leg cracking causing falls. Consumers must stop using and return forks for free replacement.
Advanced CompositesJun 16, 2017 - Use cautionVehicle
CHEVROLET SS (2016) recall — Steering
GM recalls 2014-2016 Chevrolet SS vehicles with potential power steering loss causing increased crash risk. Owners must have steering gear inspected and replaced free by dealers.
ChevroletJun 15, 2017 - Use cautionMedical device
ICU Medical Inc recalls Plum 360 Infusion System
ICU Medical recalls Plum 360 Infusion System Model 30010 due to risk of connectivity module disengaging, causing shutdown without alarm. Affected units may delay therapy or interrupt infusions.
ICU MedicalJun 15, 2017 - Lower riskMedical device
Boston Scientific Corporation recalls Encore(TM) 26 Inflation Device, REF Catalog Nos.: (a) H74904526011, (b) M001151050, (c) M00566670, (d) M0067101140
Boston Scientific recalls Encore 26 Inflation Devices with specific catalog and serial numbers due to reported cracked trays. Consumers should check their device details to determine if affected.
Boston ScientificJun 15, 2017 - Use cautionMedical device
Fujifilm Medical Systems U.S.A., Inc. recalls FUJIFILM FDR Visionary Suite with CH-200. Model # CH-200, Catalog: Visionary Suite (FMSU Marketing Name) The FDR
Fujifilm recalls FDR Visionary Suite X-ray systems with CH-200 model due to potential cracks in the tube holding shaft that could lead to injury. Affected units have specific serial numbers and UDI codes.
Fujifilm Medical SystemsJun 15, 2017
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