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 riskDrug
Taro Pharmaceuticals U.S.A., Inc. recalls Phenytoin Oral Suspension USP, 125 mg/5 mL potency, 8 fl oz (237 mL) Rx Only Mfd. by: Taro Pharmaceuticals Industries
Taro Pharmaceuticals recalls Phenytoin Oral Suspension USP 125mg/5mL due to potential coagulation and failure to resuspend as per label instructions. Affected lots may not mix properly after shaking.
Taro PharmaceuticalsFeb 7, 2020 - Lower riskFood
PNW Veg Co LLC recalls Foodservice item, Norpac Catalog Number 08099, frozen FLAV-R-PAC Roasted Spicy Potatoes O'brien, 6/40 oz. (2.5 lbs.)
PNW Veg Co recalls frozen FLAV-R-PAC Roasted Spicy Potatoes O'brien (Norpac 08099) for undeclared wheat and soy. Consumers should check labels and contact the company for details.
PNW Veg CoFeb 7, 2020 - Use cautionFood
Lindt & Sprungli (USA), Inc. recalls Lindt Excellence 85% Cocoa Dark Chocolate Bars, 3.5 oz.(100g)
Lindt Excellence 85% Cocoa Dark Chocolate Bars (3.5oz) recalled due to potential undeclared milk allergens exceeding New York State thresholds. Consumers should check lot codes and contact for details.
LindtFeb 7, 2020 - Lower riskFood
Vitamin Cottage Natural Food Markets, Inc. recalls Natural Grocers Organic Extra Virgin Coconut Oil, packaged in glass jars with metal lids and a plastic shrink seal,
Natural Grocers recalls organic coconut oil in glass jars with metal lids due to mold testing. Consumers should check UPC# 849327-000368 and batch code HBC-0919 for affected units.
Natural GrocersFeb 7, 2020 - Use cautionVehicle
BENTLEY BENTAYGA (2019) recall — Fuel System, Gasoline
Bentley is recalling 2019-2020 Bentayga vehicles with a fuel line quick connector that may leak, increasing fire risk. Owners must have the fuel line replaced free of charge.
BentleyFeb 6, 2020 - Lower riskMedical device
Deroyal Industries, Inc. Lafollette recalls Teleflex Pilling Aortic Punch, 4.0mm. Sterile, Rx Only, disposable. Included as part of Intl-Cardiac Surgery Kit -
Deroyal Industries recalls Teleflex Pilling Aortic Punch 4.0mm devices due to potential sterile packaging compromise. This surgical device, used in cardiac procedures, may be unsafe if packaging is damaged.
Deroyal IndustriesFeb 6, 2020 - Lower riskMedical device
Invivo Corporation recalls Monitor for the Functional Imaging System for Magnetic Resonance Imaging System
Invivo recalls specific MRI monitor models due to insufficient shielding of Philips SensaVue DVI Adapter, which may cause interference with MRI safety systems.
InvivoFeb 6, 2020 - Lower riskMedical device
Baxter Healthcare Corporation recalls Prismaflex System, Prismaflex Control Unit
Baxter Healthcare recalls Prismaflex System and Control Units for proper connector use per operator manual. No immediate action needed but follow manual guidelines to prevent misuse.
Baxter HealthcareFeb 6, 2020 - Lower riskFood
Forest View Bakery recalls Forest View Bakery Cheesecake with Poppy seeds in 18oz plastic clam shell UPC 745454333860
Forest View Bakery recalls 18oz cheesecake with poppy seeds due to undeclared milk, almonds, and wheat allergens. Consumers should avoid this product to prevent allergic reactions.
Forest View BakeryFeb 6, 2020 - Stop using nowFood
New Seasons Market LLC recalls Vegetarian Lasagna With Gluten-Free Pasta, New Seasons Market brand. Product is packaged in a grab "n" go aluminum
New Seasons Market recalls Vegetarian Lasagna with gluten-free pasta due to undeclared soy. Check your product for the correct label and sell-by dates.
New Seasons MarketFeb 6, 2020 - Stop using nowConsumer product
Sun Organic Recalls Wintergreen Essential Oils Due to Failure to Meet Child Resistant Packaging Requirements; Risk of Poisoning
Sun Organic recalls Wintergreen essential oils sold before April 2019 due to lack of child-resistant caps. Get a free replacement cap or store safely.
Sun OrganicFeb 6, 2020 - Stop using nowConsumer product
Star Water Systems Recalls Sump Pumps Due to Fire Hazard
Star Water Systems recalls pedestal sump pumps with specific model numbers and date codes due to fire risk from overheating. Consumers must unplug and get a refund.
Star Water SystemsFeb 6, 2020 - Stop using nowConsumer product
Rooms To Go Recalls Patmos Chaise Lounge Chairs Due to Violation of Federal Lead Paint Ban (Recall Alert)
Rooms To Go recalls Patmos Chaise Lounge Chairs due to lead paint violations. Stop using immediately and contact the company for a replacement.
Rooms To GoFeb 6, 2020 - Use cautionConsumer product
Rawlings Recalls Catcher's Helmets Due to Risk of Head Injury
Rawlings recalls CHMACH-SR Senior Catchers helmets due to potential head injury risk from back plate failure. Affected helmets have 'MACH' on hangtag and 'CHMACH-SR-RevA' sticker inside.
RawlingsFeb 6, 2020 - Stop using nowConsumer product
Juratoys Recalls Bead Maze Toys Due to Choking Hazard
Juratoys recalls Sophie la Giraffe Bead Maze toys due to small parts that pose a choking hazard to young children. Consumers should stop using and destroy the triangle piece if it matches recalled batch numbers.
JuratoysFeb 6, 2020 - Stop using nowConsumer product
Infantino Recalls Infant Carriers Due to Fall Hazard
Infantino recalls specific infant carriers with broken buckles that could cause falls. Consumers must stop using and get free replacements.
InfantinoFeb 6, 2020 - Stop using nowConsumer product
Country Home Products Recalls DR Walk Behind Leaf Blowers Due to Projectile Hazard
DR Power Equipment recalls walk behind leaf blowers due to blades breaking off and becoming projectiles. Stop using immediately for a full refund.
DR Power EquipmentFeb 6, 2020 - Lower riskMedical device
bioMerieux, Inc. recalls VITEK 2 card AST-N371 - Product Usage: The VITEK 2 is an automated system consisting of instruments, software, and
Biomerieux recalls VITEK 2 AST-N371 reagent cards due to compromised pouch seals risking moisture exposure that could affect antibiotic test results. Affected units include specific lot numbers from 2021.
BiomerieuxFeb 5, 2020 - Use cautionMedical device
Siemens Healthcare Diagnostics, Inc. recalls IMMULITE 2000 Systems E2 Estradiol Catalog #: US: L2KE22(D) (200 tests) and L2KE26(D) (600 tests) and OUS: L2KE22 (200
Siemens Healthcare recalls IMMULITE 2000 Estradiol tests that may give false high results, risking delayed cancer treatment. Affected units include specific catalog numbers and manufacturing lots.
Siemens HealthcareFeb 5, 2020 - Lower riskDrug
Pfizer Inc. recalls Caduet (amlodipine besylate/atorvastatin calcium) Tablets, 10 mg/20 mg*, 30-count bottle, Rx only, Distributed by:
Pfizer recalls Caduet 10mg/20mg tablets due to potential defective packaging that may not seal properly, risking moisture exposure. Affected products were distributed with specific lot numbers and expiration dates.
PfizerFeb 5, 2020 - Lower riskMedical device
LivaNova USA Inc recalls VNS Therapy Programmer, Model 3000 used with Models 103, 104, 105, 106, or 8103 VNS Therapy generators.
LivaNova recalls VNS Therapy Programmer Model 3000 (v1.6) used with specific VNS generators due to false positive warnings that may cause unnecessary medical procedures. Affected users should contact LivaNova for guidance.
LivaNovaFeb 4, 2020 - Use cautionMedical device
Wilson-Cook Medical Inc. recalls HEMO-7 Hemospray Endoscopic Hemostat
Wilson-Cook recalls HEMO-7 Hemospray Endoscopic Hemostats with cracked handles that may cause carbon dioxide cartridge to exit during use. Affected units from Jan 2017 to Jan 2020 need inspection.
Wilson-Cook MedicalFeb 4, 2020 - UnratedMedical device
Deroyal Industries, Inc. Lafollette recalls DeRoyal Sterile Custom Kits containing Cardinal Health Gowns. Sold as the following: ASC Thyroid Pack 89-6302.14
DeRoyal recalls sterile custom kits with Cardinal Health gowns due to unknown bioburden and contamination risks. Affected kits include ASC Thyroid Pack 89-6302.14 with specific lot numbers. Consumers should check their kit details and contact DeRoyal for guidance.
DeRoyalFeb 4, 2020 - Use cautionMedical device
CareFusion 303, Inc. recalls CareFusion Alaris System, Alaris PC unit models 8000 and 8015 (UDI: 10885403801518)
CareFusion recalls Alaris PC units 8000 (v9.5 or older) and 8015 (v12.1.0 or 9.33 or older) due to software errors that could interrupt insulin therapy. Affected users should check their device version and contact CareFusion for updates.
CareFusionFeb 4, 2020 - Stop using nowFood
Whole Foods Market recalls Dark Chocolate Dipped Almond Horn Cookie sold by the individual cookie packaged in Self Serve and Plastic clam shell
Whole Foods Market recalls Dark Chocolate Dipped Almond Horn Cookies due to undeclared milk. Check your PLU and best-by date for details.
Whole Foods MarketFeb 4, 2020 - Lower riskMedical device
Conformis, Inc. recalls iTotal PS Knee Replacement System, Model No. TPS-111-1111-010101, (ITOTAL PS IPOLY IMPLANT KIT LEFT) Product Usage: The
Conformis recalls a limited number of iTotal PS knee replacement systems with incorrect serial numbers delivered to the wrong customers. This does not pose a safety risk but requires correction of labeling.
ConformisFeb 3, 2020 - Lower riskMedical device
Radiometer Medical ApS recalls ABL90 FLEX PLUS Analyzer, Model Number 393-092 - Product Usage: It is intended for use in a laboratory environment,
Radiometer recalls ABL90 FLEX PLUS analyzers with software below 3.4 MR2 due to barcode misreads causing patient mixups and sample loss. Affected units may delay medical treatment.
RadiometerFeb 3, 2020 - UnratedMedical device
Materialise N.V. recalls TRUMATCH Orthognathic - Full Bimaxillary Surgical Kit, Catalog Number SD980.001
Materialise recalls TRUMATCH Orthognathic Full Bimaxillary Surgical Kit (SD980.001) due to custom surgical plate not matching package labeling. Affected units may have incorrect plate design.
MaterialiseFeb 3, 2020 - Lower riskMedical device
Dexcom Inc recalls Dexcom G6 Continuous Glucose Monitoring System The Dexcom G4 PLATINUM Continuous Glucose Monitoring System is a glucose
Dexcom recalls G6 glucose monitors that may give false high readings when used with hydroxyurea. Affected models include G6 Sensor Kits sold from 2020 onward. No action needed if not using hydroxyurea.
DexcomFeb 3, 2020 - Stop using nowDrug
Pfizer Inc. recalls Fentanyl Citrate Inj., USP 100 mcg Fentanyl/2 mL (50 mcg/mL), 2 mL Single-dose Vial, Each Tray contains 25 Vials,
Pfizer recalls Fentanyl vials with loose metal seals that may compromise sterility. Affected vials have specific lot numbers and expiration dates. Stop using immediately if you have these vials.
PfizerFeb 3, 2020
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