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
35,025 found- Lower riskMedical device
Roche Diagnostics Operations, Inc. recalls cobas infinity central lab running software version 3.01.03 through 3.02.08, Catalog#: 07154003001
Roche recalls cobas infinity lab software versions 3.01.03 to 3.02.08 due to potential false positive or negative test results in specific user scenarios. Affected systems may need software updates to prevent incorrect lab results.
RocheJun 24, 2021 - Stop using nowMedical device
CardioQuip, LLC recalls CardioQuip, Modular Cooler-Heater 1000(i), Refrigeration Module, Model: MCH-10RMS, UDI: (01)00860000846127 used with
CardioQuip recalls MCH-10RMS refrigeration modules used in surgery due to potential bacterial growth in water systems that could infect patients during procedures.
CardioQuipJun 24, 2021 - Lower riskFood
Greenwood Ice Cream recalls JERSEY COOKIE MONSTER ICE CREAM 3 GALLONS (11.34 LITERS) MFG: GREENWOOD ICE CREAM CO LTD 4829 PEACHTREE ROAD, ATLANTA,
Greenwood Ice Cream recalls 3-gallon Jersey Cookie Monster ice cream due to undeclared soy in the product. Consumers should check lot numbers for affected items.
Greenwood Ice CreamJun 24, 2021 - Lower riskFood
Avanti Frozen Foods recalls Cooked, Peeled and Deveined, Tail-on, Shrimp. CENSEA, Frozen Cooked, peeled and deveined, Tail Off Shrimps IQF 2 LB
Avanti Frozen Foods recalls cooked, peeled and deveined shrimp products due to potential Salmonella contamination. Consumers should check product labels for affected items and discard or return them.
Avanti Frozen FoodsJun 24, 2021 - Use cautionConsumer product
Plant Guru Recalls Wintergreen, Birch and Blends of Essential Oils Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
Plant Guru recalls wintergreen, birch, and headache relief essential oils due to non-child-resistant packaging, risking poisoning if young children swallow. Consumers must stop using and return for refunds.
Plant GuruJun 24, 2021 - Stop using nowConsumer product
La Paloma Recalls Girls' Nightgowns Due to Violation of Federal Flammability Standard; Burn Hazard (Recall Alert)
La Paloma recalls girls' nightgowns that fail federal flammability standards, risking burns. Consumers must stop using and get a refund.
La PalomaJun 24, 2021 - Use cautionConsumer product
Gramr Recalls Brushed Gold Tea Kettles Due to Burn Hazard (Recall Alert)
Gramr recalls brushed gold tea kettles from winter CAUSEBOX subscription boxes due to burn hazard from hot water and steam expulsion during use.
GramrJun 24, 2021 - Use cautionVehicle
NISSAN TITAN (2020) recall — Exterior Lighting
Nissan is recalling certain 2020-2021 Titan and Versa vehicles with potentially cracked turn signal bulbs that may fail to illuminate, increasing crash risk. Owners should contact Nissan for free bulb replacement.
NissanJun 23, 2021 - Use cautionVehicle
LAMBORGHINI HURACAN (2020) recall — Back Over Prevention
Lamborghini recalls 2018-2021 Huracan vehicles with rearview camera software error that may cause crashes in cold temperatures. Fix available via free software update.
LamborghiniJun 23, 2021 - Use cautionMedical device
Covidien Llc recalls Covidien Sonicision Reusable Generator-converts electrical power from the battery pack to ultrasonic energy to drive
Covidien recalls specific Sonicision Reusable Generators due to potential manufacturing errors that may cause device failure, leading to injury risks like burns or tissue damage during medical procedures.
CovidienJun 23, 2021 - Lower riskMedical device
Beckman Coulter, Inc. recalls Kaluza C Flow Cytometry Software Versions: 1.0*, 1.1.1 and 1.1.2 Kits: C10574 - Kaluza C Single Perpetual License
Beckman Coulter recalls Kaluza C Flow Cytometry Software versions 1.0, 1.1.1, and 1.1.2 kits that may generate erroneous results. Affected users should contact for updates.
Beckman CoulterJun 23, 2021 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls TJM6008 Jamshidi" Crown Bone Marrow Biopsy/Aspiration Needle with Marrow Acquisition Cradle. 8G x 15 cm; TJC3513
Bard recalls Jamshidi bone marrow biopsy needles due to incomplete packaging seals that may allow non-sterile product. Affected models include TJM6008 and TJC3513. Consumers should check serial numbers and contact Bard for details.
BardJun 23, 2021 - Lower riskDrug
Partner Therapeutics Inc recalls LEUKINE (Sargramostim) for Injection, 250 mcg/ vial, 5mL vials, 5 (250 mcg vials) per box, Rx only, Mfd by Partner
Partner Therapeutics recalls LEUKINE (sargramostim) 250 mcg vials due to stability failure at 27 months. This may affect patients using the product for cancer treatment.
Partner TherapeuticsJun 23, 2021 - Stop using nowFood
H & H Products Company recalls Hartley's brand Worcestershire sauce in 1 gallon plastic bottles and 50 gallon drums.
H & H Products recalls Hartley's Worcestershire sauce due to undeclared fish (anchovies). Check lot numbers if you bought from FL, AL, or GA distributors.
Hartley'sJun 23, 2021 - Use cautionMedical device
BioMerieux SA recalls MYLA software. Used to manage microbiology test workflow from the reception of requests to the transmission of results
BioMerieux recalls MYLA software versions 4.7.0-4.8.1 for potential unwanted result alterations when using BCI Connect. Affected users should contact for remedy.
BioMerieuxJun 22, 2021 - Use cautionDrug
Ardil Comercial S.R.L. recalls Limar Hand Sanitizer, Isopropyl Alcohol 70%, Cont. 4 oz bottles, Manufactured in Dominican Republic: by Ardil Comercial
Ardil Comercial recalls 4 oz isopropyl alcohol hand sanitizer bottles that resemble drinking water bottles, posing a risk of accidental ingestion by children.
Ardil ComercialJun 22, 2021 - Lower riskDrug
HOYU(US) LOGISTICS INC recalls QiYu Hand Sanitizer (ethyl alcohol 75% (v/v)), 16.9 FL OZ (500 ML) bottles, Manufactured by: Guangzhou Minghui
HOYU(US) Logistics Inc recalls QiYu hand sanitizer bottles with 75% alcohol content due to subpotent levels. This may not effectively kill germs. Consumers should check product details and contact the company for guidance.
QiYuJun 22, 2021 - UnratedDrug
Teligent Pharma, Inc. recalls Erythromycin Topical Gel, 2%, Net Wt. (a) 30 g,(NDC 52565-033-30) (b) 60 g,(NDC 52565-033-60) Rx Only, Manufactured by:
Teligent Pharma recalls 2% Erythromycin Topical Gel (30g/60g) due to failed impurities. Rx-only products with specific NDCs and lots may pose risks. Consumers should contact for details.
Teligent PharmaJun 22, 2021 - Lower riskFood
Southern Classic Food Group LLC recalls Milo's Sauce 5 gallon pails 24 pails per pallet
Southern Classic Food Group recalls Milo's Sauce 5-gallon pails (lot numbers 1148, 1169, 1165, 1158) due to undeclared fish allergen. Consumers should check product labels and contact the company for details.
Southern Classic Food GroupJun 22, 2021 - Lower riskFood
Del Monte Foods, Inc recalls Del Monte Fresh Cut Golden Sweet Whole Kernel Corn; 15.25 oz. can (24 x 15.25 oz. cans per case) Case UPC
Del Monte recalls 15.25 oz. corn cans with post-process spoilage found during distribution. Consumers should check UPCs and lot numbers for affected products.
Del MonteJun 22, 2021 - Lower riskMedical device
Murata Vios, Inc. recalls muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachometer and alarm rate
Murata Vios recalls Model 2050 bedside cardiac monitors with software versions 1.49.02 and 1.52.00. Distorted ECG waveforms and flickering vital signs may occur during setup, potentially causing inaccurate readings.
Murata ViosJun 21, 2021 - Use cautionMedical device
Accora Inc recalls Configura Advance Chair, Model Number: CHAIR-0-SC1-030; Advance Chair, 100mm Castors, Std Backrest, Manual; Serial
Accora recalls Advance Chairs with serial numbers 10001-SC1-20 to 10570-SC1-21 and other models due to potential backrest detachment. Consumers should check their serial numbers and contact Accora for details.
AccoraJun 21, 2021 - UnratedMedical device
Delta Med SpA recalls NEO DELTA Self Safe 1, I.V. Catheter with PUR REF 3708122, Lot 00A1160627 5000 units
Delta Med recalls 5000 units of NEO DELTA Self Safe 1 IV catheters with PUR REF 3708122, Lot 00A1160627 due to possible missing sterility. Consumers should check their catheters for this specific model and lot number.
Delta MedJun 21, 2021 - Lower riskDrug
Prairie Wolf Spirits recalls Prairie Wolf Distillery Alcohol Antiseptic 80%, Topical Solution Hand Sanitizer, packaged in a) (16.9oz) 500 mL (UPC 8
Prairie Wolf Spirits recalls 80% alcohol hand sanitizer bottles that look like beverage containers to prevent accidental ingestion by children.
Prairie Wolf SpiritsJun 21, 2021 - Lower riskFood
Bazzini LLC recalls Trader Joes Dark Chocolate Almond Butter Cup, 1.4 oz. (2-20-gram cups per pack), PVC Pouch, 72 packs per case; 2 cups
Trader Joe's Dark Chocolate Almond Butter Cups (1.4 oz) may contain undeclared peanut allergen. Consumers should check packaging for recall codes and contact the company for details.
BazziniJun 21, 2021 - Lower riskFood
Eat Gangster, LLC recalls Eat GANGSTER, Oatmeal Schmoatmeal Cookie Mix, 8.5 Oz, Eat GANGSTER LLC, Wichita, KS, UPC 0 51497 13952 0
Eat Gangster recalls Oatmeal Schmoatmeal Cookie Mix due to potential Salmonella contamination in tigernut flour. Consumers should check best-by dates and contact the company for details.
Eat GangsterJun 21, 2021 - Lower riskFood
Bea Lydeckers Naturals Inc recalls Living Free Nerve & Muscle Plus Cetyl-Myristoleate Herbal and Glandular Supplement, 180 and 500 capsules per bottles.
Bea Lydeckers Naturals recalls Living Free Nerve & Muscle supplements due to missing soy lecithin labeling on product labels. Consumers should check for white HDPE bottles with threaded lids.
Bea Lydeckers NaturalsJun 21, 2021 - Use cautionMedical device
Respironics California, LLC recalls Philips Respironics V60 Plus Ventilator with Software Versions 3.00 and 3.10. The Respironics V60/V60 Plus Ventilator
Class I recall of Philips Respironics V60/V60 Plus Ventilators (Software 3.00/3.10) distributed worldwide and in the U.S. on June 18, 2021.
RespironicsJun 18, 2021 - Lower riskMedical device
Remel Inc recalls ThermoScientific Oxoid Antimicrobial Susceptibility Discs Rx only Made in the United Kingdom
Remel recalls Oxoid Antimicrobial Susceptibility Discs (UK-made) with specific model and lot numbers due to out of specification. Consumers should check their product details to determine if affected.
RemelJun 18, 2021 - Stop using nowMedical device
WOM World of Medicine AG recalls Covidien HysteroLux Fluid Management System Control Unit, REF: 72205000
Covidien recalls HysteroLux Fluid Management System Control Units with serial numbers starting 1803CE... that freeze display at 32450 ml, risking fluid distention. Stop using immediately.
CovidienJun 18, 2021
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