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
35,006 found- UnratedMedical device
Hager & Meisinger Gmbh recalls SINGLES Carbide US-No. FG556; UDI +E0HM26000313140091; STERILE R; Size 009, Length 3.8; 2025-03-18 - Product Usage:
Hager & Meisinger recalls SINGLES Carbide US-No. FG556 dental devices due to potential US-dates mismatch between package label and bar code. Affected units have specific identifiers and usage for dental procedures.
Hager & MeisingerJul 15, 2020 - Lower riskMedical device
Stimwave Technologies Inc recalls StimQ Peripheral Nerve Stimulator System (PNS) Models FR4A-SPR-BO US - Product Usage: is used for peripheral neural
Stimwave recalls StimQ PNS Models FR4A-SPR-BO US due to a non-functional component not listed in product labeling. Affected units have specific serial numbers.
StimwaveJul 15, 2020 - Lower riskFood
Happy Colon Foods recalls Happy Colon MMMM Chocolate Chip Cookie 0.98oz UPC 56817 00703
Happy Colon Foods recalls 0.98oz MMMM Chocolate Chip Cookies (UPC 56817 00703) due to undeclared milk content, which may cause allergic reactions in sensitive individuals.
Happy Colon FoodsJul 15, 2020 - Use cautionFood
Winter Gardens Quality Foods, Inc. recalls Whole Foods Spinach Artichoke Dip ,4-12 oz containers, Lot # 248 Manufactured on 7/8/2020 Use By: 07/26/2020
Winter Gardens recalls spinach artichoke dip containers from July 2020 due to undeclared egg allergen. Consumers should check lot numbers and contact the company for details.
Winter GardensJul 15, 2020 - Use cautionConsumer product
Nutraceutical Recalls Simplers Botanicals Wintergreen Essential Oil Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning
Simplers Botanicals Wintergreen Essential Oil lacks child-resistant packaging, risking poisoning for young children. Consumers must store out of reach and contact for refund/disposal.
Simplers BotanicalsJul 15, 2020 - Stop using nowConsumer product
Crate and Barrel Recalls Parke Twin and Full Beds Due to Fall Hazard
Crate and Barrel recalls Parke twin and full platform beds with wood headboards that can separate from side rails, causing fall hazards. Consumers must stop using and return for free replacement.
Crate and BarrelJul 15, 2020 - Use cautionVehicle
JAYCO REDHAWK (2018) recall — Equipment
Jayco is recalling 2016-2018 Redhawk and Greyhawk motorhomes due to potential pump bracket failure causing hydraulic fluid leaks or detachment, increasing crash risk.
JaycoJul 14, 2020 - Use cautionVehicle
FCCC XCR (2020) recall — Electrical System
Daimler Trucks North America recalls 2016-2020 FCCXCR vehicles with faulty rear lights that may cause crashes. Owners must get free PDM replacement.
DTNAJul 14, 2020 - Lower riskMedical device
GE Healthcare, LLC recalls CARESCAPE R860 Ventilator The CARESCAPE R860 ventilator is a microprocessor based, electronically controlled,
GE Healthcare recalls CARESCAPE R860 ventilators with potential oxygen sensor issue causing inaccurate FiO2 display. Affected units have specific identifiers; check your device's serial number. No immediate action needed but monitor for incorrect oxygen readings.
GE HealthcareJul 14, 2020 - Lower riskMedical device
Smiths Medical ASD Inc. recalls CADD Administration Sets, Model #21-7346-24
Smiths Medical recalls CADD Administration Sets (Model #21-7346-24) with potential incorrect air filter assembly. Affected units include specific lot numbers. Consumers should check their product details.
Smiths MedicalJul 14, 2020 - Lower riskMedical device
Thomas Scientific recalls Wuxi Nest, model numbers 202115, 202117, 202017, 202018 - Product Usage: Patient specimen collection.
Thomas Scientific recalls Wuxi Nest tubes (models 202115, 202117, 202017, 202018) used for patient specimen collection due to potential safety risks. Affected lots include 060620MB1 through 062220D02. Consumers should check their product details and contact Thomas Scientific for replacement.
Thomas ScientificJul 14, 2020 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls Cios Alpha (VA20) - Model: 10308191 Cios Alpha (VA30) - Model: 11105200 Cios Spin (VA30) - Model: 10308194 Cios Alpha
Siemens recalls specific models of Cios Alpha and Spin mobile X-ray systems due to a hardware error that can cause permanent loss of imaging functionality if hot plugging is used on older generator revisions.
SiemensJul 14, 2020 - Lower riskMedical device
Olympus Corporation of the Americas recalls Smart Stapes Protheses Piston 0.6mm X 4.25 mm- Partial Ossicular Replacement Catalog Number: 70143662
Olympus recalls Smart Stapes Protheses Piston 0.6mm X 4.25mm (Catalog 70143662) due to mislabeled outer carton. This could lead to incorrect product use.
OlympusJul 14, 2020 - Lower riskMedical device
Inpeco S.A. recalls Accelerator a3600 Automation System with the Aliquoter Module (Inpeco P/N FLX-212) The FlexLab (aka Accelerator a3600
Inpeco recalls Accelerator a3600 Automation Systems with Aliquoter Module (FLX-212) that may dilute samples during error handling, leading to inaccurate lab test results. Affected units have specific firmware versions and serial numbers.
InpecoJul 14, 2020 - UnratedDrug
Soluciones Cosmeticas, SA de CV recalls Bersih Hand Sanitizer Gel, Net wt. 16.9 floz (500ml), Blue and Green cap) Distributed by RediBag USA 135 Fulton Ave New
Soluciones Cosmeticas recalls Bersih Hand Sanitizer Gel due to cGMP deviations. Affected units have blue or green caps and were distributed by RediBag USA. Consumers should check their product details.
Soluciones CosmeticasJul 14, 2020 - Lower riskDrug
Teva Pharmaceuticals USA recalls Lidocaine Patch 5%, packaged in 30-count cartons, Rx only, Manufactured by: Actavis Laboratories UT, Inc., Salt Lake
Teva Pharmaceuticals USA recalls Lidocaine 5% patches with missing or incorrect lot/expiration dates on individual pouches. This labeling issue may lead to incorrect medication use. Consumers should check their patches for the lot and expiration date.
Teva Pharmaceuticals USAJul 14, 2020 - Use cautionVehicle
MITSUBISHI OUTLANDER PHEV (2019) recall — Seat Belts
Mitsubishi recalls 2019 Outlander PHEV vehicles with second-row seat belt buckle interference that may cause buckles to become unfastened during crashes.
MitsubishiJul 13, 2020 - Use cautionMedical device
Aesculap Implant Systems LLC recalls ENNOVATE MIS REMOVALKEY SHORT, product code SZ380R
Aesculap recalls ENNOVATE MIS Removal Key Short (SZ380R) due to risk of spinal fixation arm fracture if 90-degree angle not met during use. Affected users should contact for details.
Aescul: Aesculap Implant Systems LLCJul 13, 2020 - Lower riskMedical device
Medtronic Inc. recalls Medtronic SynchroMed, Model A10
Medtronic recalls SynchroMed Model A10 devices with software version 1.1.300 due to missing decimal separator in parameter displays, potentially causing misinterpretation of values.
MedtronicJul 13, 2020 - Lower riskMedical device
OraSure Technologies, Inc. recalls Orasure Technologies Interept Benzodiazopene Miro-Plate EIA-Benzo EIA 2 plate Matrix Oral Fluid Coated Micro-Plate. IVD
OraSure recalls certain Benzodiazepine test kits due to incorrect lot numbers on calibrators and unit boxes. This may lead to inaccurate results. Check your kit's lot number and contact OraSure for details.
OraSureJul 13, 2020 - UnratedMedical device
Ortho-Clinical Diagnostics recalls VITROS XT Chemistry Products TBIL-ALKP Slides (ALKP is not affected) In Vitro Diagnostic use only - The TBIL test
Ortho-Clinical Diagnostics recalls VITROS XT TBIL-ALKP Slides due to etrombopag interference in TBIL tests. This affects in vitro diagnostic use only. No remedy specified in official notice.
Ortho-Clinical DiagnosticsJul 13, 2020 - Lower riskDrug
Fresenius Kabi USA, LLC recalls Fosaprepitant for Injection, 150 mg / vial in a 10 mL Single-Dose vial, Rx only, Fresenius Kabi, Lake Zurich, IL 60047;
Fresenius Kabi recalls Fosaprepitant injection vials with incorrect EDTA labeling. This labeling error may affect medication accuracy. Affected vials have specific NDC and lot numbers. Contact for details.
Fresenius KabiJul 13, 2020 - Lower riskDrug
Bausch Health Companies, Inc. recalls Hydrocortisone butyrate Cream, 0.1%, 15-gram tubes, Rx Only, Manufactured for Oceanside Pharmaceuticals a division of
Bausch Health recalls hydrocortisone butyrate cream 0.1% 15g tubes (Rx only) due to subpotent drug risk. This means the medication may not provide intended treatment. Affected lots manufactured for Oceanside Pharmaceuticals.
Bausch HealthJul 13, 2020 - Lower riskFood
Siam Trading Inc. recalls Khaotan Rice Cracker, Net Wt. 150g
Siam Trading Inc. recalls Khaotan Rice Cracker (150g) due to undeclared cashews. Consumers should check product codes or best by dates for affected items.
Siam TradingJul 13, 2020 - Lower riskFood
Lopez Gonzalez Santana Corporation recalls BTREX PLUS, Dietary Supplement 2 Caplets, UPC 05380930802 (Physician Samples)
Lopez Gonzalez Santana recalls BTREX PLUS dietary supplement 2 caplets (UPC 05380930802) due to damaged tablets in physician samples. Consumers should check lot numbers 32179 (exp 9/2022) and 33278 (exp 12/2022).
Lopez Gonzalez SantanaJul 13, 2020 - Lower riskFood
Flagstone Foods LLC recalls Wegmans PECAN BLEND Supreme Pecans, Cashews & Pistachios NET WT 16 OZ(1 LB) 454g plastic bag Ingredients: Pecans,
Wegmans recalls 16oz pecan blend with undeclared almonds and walnuts. Consumers should check labels for these ingredients and avoid use if they have allergies.
WegmansJul 13, 2020 - Use cautionVehicle
INFINITI Q70 (2014) recall — Power Train
Infiniti is recalling 2014 Q70 models with a potential driveshaft break that could cause loss of propulsion or disable the parking brake, increasing crash risk. Owners will receive free driveshaft replacement.
InfinitiJul 12, 2020 - Use cautionVehicle
EAST TO WEST SILVER LAKE (2021) recall — Equipment
Forest River recalls 2021 East to West Silver Lake trailers due to grill fire risk when stowed with propane hose attached and burners on. Owners must have propane hose repositioned to prevent fire.
Forest RiverJul 12, 2020 - Stop using nowDrug
4e Brands North America, Llc recalls Modesa instant HAND SANITIZER with moisturizers & vitamin E, (70% ethyl alcohol), 33.8 FL OZ (1 L) bottle, Distributed
4e Brands recalls Modesa hand sanitizer due to CGMP deviations and potential methanol contamination. Check your bottle lot and expiry date.
ModesaJul 11, 2020 - Use cautionVehicle
LANCE TRAVEL TRAILER (2020) recall — Equipment
Lance Camper is recalling 2018-2021 trailers with specific propane stoves due to potential gas leaks that could cause fire. Owners should contact customer service for repairs.
Lance CamperJul 10, 2020
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