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 riskMedical device
Abbott Gmbh & Co. KG recalls LN 3R70-01; software version 2.6.2 and earlier. The software is used with the Alinity i (LN 03R65-01) processing module
Abbott recalls Alinity i devices with software version 2.6.2 and earlier due to potential performance issues. Affected users should contact Abbott for details.
AbbottJan 24, 2020 - Lower riskDrug
Macleods Pharma Usa Inc recalls Pioglitazone and Metformin Hydrochloride Tablets, USP 15 mg/500 mg, Rx Only, 60-count bottle, Manufactured for Macleods
Macleods Pharma recalls 15mg/500mg Pioglitazone and Metformin tablets due to subpotent drug levels. These prescription pills may not contain enough active ingredients. Check your prescription bottles for lot numbers BPA5903A or BPA5819A.
MacleodsJan 24, 2020 - UnratedDrug
Breckenridge Pharmaceutical, Inc recalls Solifenacin Succinate Tablets, 10 mg, packaged in a) 30-count bottles (NDC 51991-894-33) and b) 90-count bottles (NDC
Breckenridge Pharmaceutical recalls 10mg Solifenacin Succinate tablets due to manufacturing error that may convert to a different, potentially harmful form. Affected products have specific NDC numbers and expiration dates.
BreckenridgeJan 24, 2020 - Lower riskDrug
Ascend Laboratories LLC recalls Olmesartan Medoxomil Tablets 20 mg, Rx Only, 90 Tablets per Bottle, Manufactured by: Alkem Laboratories Ltd., Mumbai -
Ascend Laboratories recalls 20mg Olmesartan Medoxomil tablets due to manufacturing errors. This medication was released with an alternate active ingredient before approval. Consumers should contact the company for details.
Ascend LaboratoriesJan 24, 2020 - Stop using nowFood
Quesos La Ricura, Ltd. recalls QUESOS LA RICURA brand Queso Cotija; Cotija Cheese; AGED OVER 60 DAYS; Ingredients: Raw Milk, Salt, Enzyme and
Quesos La Ricura recalls 640 units of Queso Cotija aged over 60 days due to possible Shiga toxin-producing E. coli contamination.
Quesos La RicuraJan 24, 2020 - Lower riskFood
Losurdo Foods, Inc. recalls 1. Boars Head Fresh Mozzarella Ball, 8oz. 2. Losurdo Fresh Caprese Log Mozzarella, 6 lbs. 3. Piancone Fresh Mozzarella
Losurdo Foods recalls fresh mozzarella products due to a production employee diagnosed with food poisoning two days after the production run. Consumers should check product lots and UPCs to determine if affected.
LosurdoJan 24, 2020 - Use cautionVehicle
CADILLAC CTS-V (2015) recall — Power Train
GM recalls 2014-2015 Cadillac CTS-V Sport vehicles with potential rear axle differential roll pin fracture causing wheel lockup and loss of control.
CadillacJan 23, 2020 - Use cautionVehicle
ROSENBAUER COMMANDER (2018) recall — Suspension
Rosenbauer is recalling 2014-2019 Commander vehicles with Reyco front suspensions due to risk of steering fluid leak and loss of power steering assist, which may cause a crash. Owners must contact customer service for free repairs.
RosenbauerJan 23, 2020 - Use cautionVehicle
RAM PROMASTER (2019) recall — Power Train
Chrysler recalls 2014-2019 Ram Promaster vehicles with 3.6L engines due to risk of unintended gear shifts causing crashes. Owners must get free transmission shift cable replacement.
RamJan 23, 2020 - Use cautionMedical device
Ra Medical Systems, Inc. recalls DABRA Laser (RA-308 Excimer Laser). The DABRA Laser and DABRA Catheter is an excimer laser ultraviolet light source and
Ra Medical recalls DABRA Laser (RA-308) systems due to software issues that could cause unintended laser light release, risking user or patient injury. Affected units have serial numbers RA00027 to RA00176.
Ra Medical SystemsJan 23, 2020 - Use cautionMedical device
Heartware, Inc. recalls HeartWare HVAD System Battery Charger The HeartWare HVAD System is indicated for hemodynamic support in patients with
Heartware recalls HVAD System Battery Charger models with potential for incorrect AC adapter insertion into HVAD Controller power port. Affected units include specific model numbers and serials listed in the recall notice.
HeartwareJan 23, 2020 - Lower riskFood
Ardent Mills LLC recalls Kroger Unbleached All Purpose Enriched Flour, 5 lb. bag. Bar code: 011110861660
Kroger Unbleached All Purpose Enriched Flour (5 lb) with bar code 011110861660 may contain Salmonella. Consumers should check lot code 112520 and use by date Nov 25, 2020.
Ardent MillsJan 23, 2020 - Stop using nowConsumer product
Varidesk Recalls Stand2Learn Stools Due to Fall Hazard
Varidesk recalls adjustable-height Stand2:Learn Stools (model 42058) due to risk of falling from broken foot support. Consumers must stop using and get a refund.
VarideskJan 23, 2020 - Use cautionConsumer product
STIHL Recalls Pressure Washers Due to Injury Hazard
STIHL recalls RE 90 pressure washers with spray wands that can disconnect during use, causing injury. Owners must stop using and get a free replacement wand.
STIHLJan 23, 2020 - Stop using nowConsumer product
PCNA Recalls Power Banks Due to Fire and Burn Hazards
Spare 10,000 mAh Power Banks with lithium-ion batteries may overheat and ignite, causing fire and burn hazards. Consumers must stop using and dispose of recalled units safely.
SpareJan 23, 2020 - Lower riskMedical device
Stryker Instruments Div. of Stryker Corporation recalls Triton Canister System (finished part numbers FG 12009, for 3L canisters, and FG 12019 for 2L canisters) Scanning Label
Stryker recalls Triton Canister Scanning Labels made before Dec 2019 due to potential underestimation of blood loss during surgery. Affected labels have specific part numbers and manufacturing dates.
StrykerJan 22, 2020 - Lower riskMedical device
Braemar Manufacturing, LLC recalls Braemar Manufacturing LLC DL950 Holter Monitor 1285 Corporate Center Dr. Suite 150 Eagan, MN 55121 USA Rx Only
Braemar recalls DL950 Holter Monitors made before January 1, 2020 that may display Error 602 and fail to start new patient studies with AAA batteries.
BraemarJan 22, 2020 - Use cautionMedical device
St Jude Medical, Cardiac Rhythm Management Division recalls Ellipse, Tiered-therapy Cardioverter/Defibrillator, REF (UDI/GTIN): CD1377-36QC (05414734507646), CD2411-36C
St Jude Medical recalls Ellipse cardioverter defibrillators with specific serial numbers that may lose wireless communication with doctors, preventing remote monitoring. Affected devices require immediate attention.
St Jude MedicalJan 22, 2020 - Lower riskMedical device
BioFire Diagnostics, LLC recalls FilmArray BCID Panel, RFIT-ASY-0126, 30, Rx Only, CE, IVD, UDI: 00815381020086 used with the following BACT/ALERT Blood
BioFire recalls FilmArray BCID Panel (RFIT-ASY-0126) used with specific BACT/ALERT blood culture bottles. False positive Proteus results may cause improper antibiotic treatment. Affected units have UDI: 00815381020086.
BioFireJan 22, 2020 - Lower riskDrug
Ascend Laboratories LLC recalls Minocycline Hydrochloride Extended-Release Tablets, USP, 105 mg*, 30-count bottle, Rx Only, Manufactured by: Alkem
Ascend Laboratories recalls 105mg Minocycline Hydrochloride Extended-Release Tablets due to failed dissolution testing. This may affect medication effectiveness. Contact for return instructions.
Ascend LaboratoriesJan 22, 2020 - Lower riskFood
Morton Salt Inc. recalls MORTON SALT;THIS SALT DOES NOT SUPPLY IODIDE; 26 oz (1LB., 10 OZ) 737 g; packed in 24 canisters per case
Morton Salt recalls 26oz non-iodide salt canisters due to undeclared iodide. Check labels for plain salt labels instead of iodized salt labels.
MortonJan 22, 2020 - Lower riskFood
Compania Nacional de Chocolates DCR S.A. recalls Granuts BBQ Mix, Net Wt/Cont. Neto 16.93 oz (480g), Contains 12 units x 1.41 oz (40g) ea. and Net Wt/Cont. Neto 6.35 oz
Compania Nacional de Chocolates recalls Granuts BBQ Mix due to undeclared wheat and soy allergens. Consumers should check lot numbers and expiration dates on the product.
Compania Nacional de ChocolatesJan 22, 2020 - UnratedMedical device
Polymer Technology Systems, Inc. recalls PTS Detect Cotinine, Ref. No. 3061, UPC 381933061017 in vitro diagnostic - Product Usage: The PTS Detect cotinine
Polymer Technology Systems recalls PTS Detect Cotinine (Ref. 3061, UPC 381933061017) due to lack of FDA 510(k) clearance for professional use. The product is no longer available in the market.
Polymer Technology SystemsJan 21, 2020 - Lower riskMedical device
Aesculap Implant Systems LLC recalls Columbus R/PS TIB.PLATEAU Cemented, various sizes, Knee implant components, model nos. NN058K NN070K NN071K NN072K
Aesculap Implant Systems LLC
AesculapJan 21, 2020 - Use cautionMedical device
Hologic, Inc. recalls Selenia Dimensions Mammography System, Model number ASY-04160, Selenia Dimensions Gantry, UDI 15420045505636,
Hologic recalls Selenia Dimensions Mammography System model ASY-04160 with serial numbers 81002143175-81003143247 due to c-arm seizing or dropping during field repairs and cleaning, posing a risk of equipment damage or injury.
HologicJan 21, 2020 - Lower riskMedical device
Medline Industries Inc recalls Medline ROBOTIC-LF REF CDS984543B Lot 20AKA927 Expiration 2020-09-30 GTIN (01)10888277056350
Medline recalls CDS984543B sterile packs due to incomplete sterilization. These packs may contain contaminants, risking infection during medical procedures. Affected units have specific lot and expiration dates.
MedlineJan 21, 2020 - Stop using nowMedical device
Sysmex America, Inc. recalls Sysmex CV-11 Sample Unit, an integrated modular sampler that conveys specimens to either the UF-5000 or UD-10 analyzers.
Sysmex recalls CV-11 Sample Units with serial numbers 11201-15620 due to urine spills causing potential smoke/sparks and fire risk. Affected units may need replacement.
SysmexJan 21, 2020 - Lower riskFood
ABH Nature's Products, Inc. recalls All Dietary Supplement manufactured and distributed by ABH Nature's Products Inc.
ABH Nature's Products recalls all dietary supplements due to violations of current good manufacturing practices. Consumers should contact the company for details.
ABH Nature's ProductsJan 21, 2020 - Use cautionVehicle
FOREST RIVER ROCKPORT (2019) recall — Structure
Forest River recalls 2014-2019 Rockport Work Trucks with potentially detachable roofs. If the roof separates, it could cause crashes. Owners must have roofs inspected by dealers free of charge.
Forest RiverJan 20, 2020 - Use cautionVehicle
FOREST RIVER GEORGETOWN (2020) recall — Equipment
Forest River recalls 2019-2020 Georgetown GTA34H5F motorhomes due to improperly routed LP gas lines near burners, risking fire. Owners must have dealer reroute the line free of charge.
Forest RiverJan 20, 2020
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