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
34,959 found- Lower riskMedical device
Abbott Laboratories Inc. (St Jude Medical) recalls TactiSys Quartz Equipment (with software version 1.7) Model: PN-004 400 Part Numbers: 600043767 (China), 100154367
St Jude Medical recalls TactiSys Quartz Equipment with software version 1.7.0 due to potential log data storage issues. Affected units may display incorrect contact force data during procedures.
St Jude MedicalApr 5, 2019 - Use cautionMedical device
Abbott Gmbh & Co. KG recalls Alinity i Processing Module, 03R65 01, with the below components. a. TED (Thermo Electric Device) Engine, Reagent
Abbott recalls Alinity i Processing Module 03R65 01 with potential loose cable connections causing temperature errors and reagent cooler failure, risking burns and shocks.
AbbottApr 5, 2019 - Stop using nowDrug
Brian P. Richardson recalls Kopi Jantan Tradisional Natural Herbs Coffee, 13g individual packages, Manufactured By: Fikrysz (M) Sdn. Bhd., Kedah,
FDA recalls Kopi Jantan coffee packages due to undeclared sildenafil and tadalafil. Check your lot and expiration date.
Kopi JantanApr 5, 2019 - Lower riskFood
Pepsico Inc recalls Diet Pepsi, Classic Diet Pepsi Taste; 12 fl. oz. cans; Sold in 6,12, 20, 24 and 36-packs 12-Pack UPC: 0 12000 17186 4:
PepsiCo recalls specific Diet Pepsi cans due to mislabeling regarding aspartame content. Check your UPCs and use-by dates for details.
PepsiApr 5, 2019 - Lower riskFood
Hercules Candy Company recalls Cashew Brittle Bits in clear 4oz bag with a Best By date of 07/14/19 and barcode number of 00369
Hercules Candy Company recalls Cashew Brittle Bits in clear 4oz bags with Best By date 07/14/19 due to possible undeclared peanuts. Consumers should check for the barcode 00369.
Hercules CandyApr 5, 2019 - Stop using nowMeat & poultry
Blount Fine Foods Recalls Ready-To-Eat Chicken Soup Product due to Misbranding and an Undeclared Allergen
Blount Fine Foods recalls frozen Homestyle Chicken Noodle Soup due to undeclared milk allergen. Do not consume or serve; return or discard immediately.
Blount Fine FoodsApr 4, 2019 - Use cautionVehicle
MAZDA MAZDA3 (2018) recall — Visibility
Mazda recalls 2016-2018 Mazda3 vehicles with a defective windshield wiper relay that may cause wipers to stop working, reducing driver visibility and increasing crash risk.
MazdaApr 4, 2019 - Use cautionMedical device
Roche Diagnostics Corporation recalls cobas p 501 post-analytical units, Part Number 05158494001. For diagnostic sample storage and retrieval.
Roche recalls cobas p 501 post-analytical units (serial 1001-1044) due to risk of tray flap detaching. This could cause sample damage or instrument malfunction.
RocheApr 4, 2019 - Lower riskMedical device
Advanced Bionics, LLC recalls SoundWave Professional Suite Software 3.2, Ref CI-6055-014, SPN 058-023-32085, UDI: (01)07630016853227, Logical
Advanced Bionics recalls SoundWave Professional Suite Software 3.2 due to installation errors when using the USB drive. Users can continue programming devices with current software versions.
Advanced BionicsApr 4, 2019 - Stop using nowConsumer product
Vivitar Recalls Hot/Cold Massage Balls Due to Burn Hazard; Sold Exclusively at Target
Vivitar recalls hot/cold massage balls that can leak or rupture during microwaving, causing burns. Return to Target for full refund.
VivitarApr 4, 2019 - Use cautionVehicle
KZRV SPORTSMEN (2019) recall — Equipment
KZRV is recalling 2019 RV models with Capital LP gas cooktops that may invert flame, causing burn injuries. Owners must replace cooktop with safe alternative.
KZRVApr 3, 2019 - UnratedMedical device
Elekta Limited recalls Elekta Unity systems Product Usage: Elekta Unity using Magnetic Resonance Imaging is indicated for radiation therapy
Elekta recalls Unity MRI systems due to unvalidated use of gadolinium contrast agents in radiation therapy. Affected units may pose risks if contrast agents are administered without proper validation.
ElektaApr 3, 2019 - Lower riskMedical device
Bio-Rad Labs recalls Autoimmune EIA Anti-Tissue Transglutaminase (tTG) IgA Test; Material Number 425-2260; Lot number 18200A - Product
Bio-Rad Labs recalls Autoimmune EIA Anti-Tissue Transglutaminase (tTG) IgA Test (Lot 18200A) due to elevated lot-to-lot bias in antibody levels. This may affect celiac disease testing accuracy but does not change clinical classifications for most samples.
Bio-Rad LabsApr 3, 2019 - Use cautionMedical device
Delfi Medical Innovations, Inc. recalls Delfi Medical Innovations, VariFit Contour Cuffs, single use adult thigh cuff, single port, single bladder, REF
Delfi Medical recalls certain VariFit Sterile Single Use Thigh Cuffs that may leak after inflation, causing blood flow. Stop using if you have the recalled model.
Delfi MedicalApr 3, 2019 - Lower riskMedical device
Becton Dickinson & Co. recalls BD Veritor System Reader -In Vitro Diagnostic for use with BD Veritor System Test Kit Devices Catalog Number: 256055
Becton Dickinson recalls BD Veritor System Reader (Catalog 256055) due to potential false test results causing misdiagnosis. Affected units have specific serial numbers listed.
Becton DickinsonApr 3, 2019 - Use cautionMedical device
Thommen Medical AG recalls Adapter for handpiece, guided, reusable, for guide sleeve 0 4.8 mm Article number: 3.04.090 - Product Usage: The
Thommen Medical recalls a dental adapter (model 3.04.090) that may deform and become difficult to remove from handpieces during use. Affected units have lot number 17415 and UDI 07640182640705.
Thommen MedicalApr 3, 2019 - Lower riskMedical device
Randox Laboratories Ltd. recalls G-6-PDH Normal Control (G-6-PDH CONTROL N), Catalogue Number PD2618 Product Usage: This product is intended for in
Randox recalls G-6-PDH Normal Control kits with incorrect target values for glucose-6-phosphate dehydrogenase testing. Affected lots may cause inaccurate blood test results.
RandoxApr 3, 2019 - UnratedMedical device
Fresenius Medical Care Renal Therapies Group, LLC recalls 2008T BlueStar Machine Software v.2.72-Hemodialysis machine Model Number: 191126 - Product Usage: The 2008T
Fresenius Medical Care recalls 2008T BlueStar hemodialysis machines with software version 2.72 due to power logic board failure risks.
Fresenius Medical CareApr 3, 2019 - UnratedDrug
AVKARE Inc. recalls Telmisartan and Amlodipine Tablets 80 mg/5 mg, 30 tablets, Rx Only, Manufactured for: AvKARE, Inc. Pulaski, TN 38478
AVKARE recalls 80mg/5mg Telmisartan and Amlodipine tablets (Rx only) due to potential impurities from long-term stability testing. These prescription blood pressure medications may pose safety risks if stored improperly.
AVKAREApr 3, 2019 - Lower riskFood
ConAgra Foods, INc. recalls Hunts Tomato Paste No Salt Added 6 ounce cans, 12 per wholesale tray Can UPC: 2700038807 Tray UPC: 2700038809
ConAgra recalls Hunts Tomato Paste No Salt Added 6oz cans due to mold risk from potential can damage. Check UPCs 2700038807 and 2700038809 for affected products.
ConAgraApr 3, 2019 - Stop using nowConsumer product
Quality Bicycle Products Recalls Bicycles Due To Injury Hazard
Recalled 2019 Salsa Warbird and Vaya bicycles have a risk of fork breakage causing injury. Consumers must stop using and return to retailer for free fork replacement.
SalsaApr 3, 2019 - Stop using nowConsumer product
Matco Tools Wireless Chargers Recalled by Professional Tool Products Due to Burn Hazard
Matco Tools wireless chargers recalled due to overheating burn hazard. Stop using and return for refund or store credit.
Matco ToolsApr 3, 2019 - Use cautionMeat & poultry
AdvancePierre Foods, Inc. Recalls Frozen Beef Patties due to Possible Foreign Matter Contamination
AdvancePierre Foods recalls 20,373 pounds of frozen beef patties that may contain soft purple plastic. Consumers should throw away or return products to the store. No injuries reported.
AdvancePierre FoodsApr 2, 2019 - Use cautionMedical device
Thermo Fisher Scientific (Asheville) LLC recalls Thermo Scientific General Purpose Dynamic Bath Precision 10L GP Bath Model Number: TSGP10
Thermo Fisher Scientific recalls 12 specific model TSGP10 baths that may malfunction due to incorrect assembly, risking overheating. Affected units have serial numbers listed in the recall notice.
Thermo FisherApr 2, 2019 - Lower riskMedical device
Ortho Organizers, Inc. recalls Maestro Orthodontic Bracket REF711-298Q QTY. 20 Rx Only (01)00190707017064 (10)889437 (422)484 Maestro Orthodontic
Ortho Organizers, Inc. recalls Maestro Orthodontic Brackets REF711-298Q and REF711-299MCQ due to mislabeling. This may cause confusion in dental treatments. Consumers should contact the manufacturer for details.
Maestro OrthodonticApr 2, 2019 - UnratedDrug
Johnson Matthey Inc. recalls Remifentanil HCl active pharmaceutical ingredient (API) for manufacturing, processing or repackaging, 416.95 g glass
Johnson Matthey recalls Remifentanil HCl active pharmaceutical ingredient due to unknown impurities exceeding safety limits. This API is used in manufacturing and repackaging. No remedy specified in official notice.
Johnson MattheyApr 2, 2019 - UnratedDrug
Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy recalls HCG 4,100 Units/vial Injection, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.
Anderson Compounding Pharmacy recalls HCG 4,100 Units/vial injections due to lack of sterility assurance. All lots are affected. Consumers should contact the pharmacy for details.
Anderson Compounding PharmacyApr 2, 2019 - Stop using nowConsumer product
Spector & Co. Recalls Power Bank Chargers Due to Fire Hazard
Spector & Co. recalls T119 Elf power bank chargers due to overheating fire hazards. Stop using immediately and contact the company for a free replacement.
Spector & Co.Apr 2, 2019 - Stop using nowConsumer product
Ocean Reef Recalls Neptune Space Integrated Diving Masks Due to Injury Hazard
Ocean Reef recalls Neptune Space Integrated Diving Masks due to restricted airflow risk. Consumers must stop using and return for free replacement or refund.
Ocean ReefApr 2, 2019 - Use cautionConsumer product
John Deere Recalls Attachment Kits for Compact Utility Tractor Snow Blowers and Brooms Due to Injury Hazard (Recall Alert)
John Deere recalls attachment kits for snow blowers and 52-inch brooms used with specific compact utility tractors due to missing operator manuals, which could cause injury. Consumers must stop using and get a manual from an authorized dealer.
John DeereApr 2, 2019
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