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Latest recalls
34,946 found- Use cautionVehicle
INTERNATIONAL MV (2019) recall — Exterior Lighting
Navistar recalls 2019 International MV trucks with combined trailer stop and turn lights that may not illuminate when brakes are used, increasing crash risk. Owners must contact Navistar for free circuit relocation.
NavistarSep 19, 2018 - Lower riskMedical device
Philips Medical Systems Gmbh, DMC recalls Philips DigitalDiagnost software 4.1.x and 4.2.x, A Stationary X-ray System Models: 712027, 712028, 712029, 712031,
Philips recalls X-ray software versions 4.1.x and 4.2.x for stationary systems with serial numbers starting 547772 to SN18000227. The software has stitching errors that may cause system interruptions during imaging.
PhilipsSep 19, 2018 - Use cautionMedical device
Encore Medical, Lp recalls Flexible Drill Shaft, FMP Acetabular System Instrumentation REF 803-05-239 RX Encore Medical, L.P.
Encore Medical recalls flexible drill shafts with lot #262667L01 due to manufacturing error that may cause drill bits to come loose during surgery, risking delays or revision surgery.
Encore MedicalSep 19, 2018 - UnratedDrug
Upsher Smith Laboratories, Inc. recalls Bumetanide Tablets, USP, 2 mg, 100-count bottle, Rx only, Manufactured by: Upser-Smith Laboratories, LLC, Maple Grove,
Upsher Smith recalls 2mg Bumetanide tablets due to failed impurities causing potential safety issues. Affected lots expire 3/31/2020 or 5/31/2020. Check your NDC number for recall.
Upsher SmithSep 19, 2018 - Use cautionDrug
Pfizer Inc. recalls Elelyso (taliglucerase alfa) for injection, 200 units/vial, single-use vial, Rx only, Distributed by Pfizer Labs,
Pfizer recalls Elelyso (taligl: 200 units/vial) injections due to loose metal ferrule crimps that may cause contamination. Affected lots include S91616. Patients should contact their doctor for guidance.
PfizerSep 19, 2018 - Use cautionFood
Baker's Service of South Florida, Inc. recalls Guava Pastry. The product is packed in a cardboard box. The firm marks the Guava Pastry option printed on the box.
Baker's Service recalls Guava Pastry due to undeclared wheat and color additives. Check your box for manufacturing dates Jul 19 through Aug 30, 2018.
Tracy BakerySep 19, 2018 - Use cautionVehicle
STARCRAFT BUS QUEST (2017) recall — Equipment Adaptive/Mobility
Forest River recalls 2017 StarCraft Quest buses with faulty wheelchair lifts that may tip users inward when exiting, increasing injury risk. Owners must contact Ricon for free cam replacement.
Forest RiverSep 18, 2018 - Use cautionMedical device
Smith & Nephew, Inc. recalls Smith+Nephew Orthopaedic Division LEGION A/P FEMORAL CUTTING BLOCK, SIZE 6 REF 71434411, QTY: (1) The LEGION AP Femoral
Smith & Nephew recalls a specific lot of Legion AP femoral cutting blocks due to an oversized spring that could cause injury during surgery.
Smith & NephewSep 18, 2018 - Lower riskMedical device
COVIDIEN LLC recalls Puritan Bennett 980 (PB980) ventilator series: Puritan Bennett" 980 Pediatric Adult Ventilator Puritan Bennett" 980
Puritan Bennett recalls 980 ventilators with serial numbers 35B1300001-35B1801541 for potential GUI display errors from USB drive performance. Owners should check serial numbers and contact the company.
Puritan BennettSep 18, 2018 - Lower riskMedical device
Baxter Healthcare Corporation recalls SPECTRUM IQ INFUSION SYSTEM WITH DOSE IQ SAFETY SOFTWARE, 3570009
Baxter recalls SPECTRUM IQ Infusion System with Doze IQ software (serials before 07/09/2018) due to false error messages when programming drugs not in the library.
Baxter HealthcareSep 18, 2018 - Lower riskMedical device
Beckman Coulter Inc. recalls The Access Cortisol Reagent. REF (Catalog Number) 33600, Lot 831755. A paramagnetic particle, chemiluminscent
Beckman Coulter recalls specific lot of cortisol reagent due to potential cross contamination causing falsely low patient results. Affected units may need replacement.
Beckman CoulterSep 18, 2018 - Use cautionDrug
Xiromed LLC recalls Altavera Levonorgestrel and Ethinyl Estradiol Tablets, USP 0.15 mg and 0.03 mg, Rx only, 3 tablet dispensers x 28
Xiromed LLC recalls Altavera tablets due to mislabeled generic names on packaging. Check your lot numbers and expiry dates for affected units.
XiromedSep 18, 2018 - Lower riskFood
Purus Labs, Inc. recalls Purus Labs MYOWHEY Premium Whey Protein, Chocolate Cookie Crunch, 75 True Servings, Net Wt. 5 lb / 2.26 kg. UPC
Purus Labs is recalling its MYOWHEY Premium Whey Protein, Chocolate Cookie Crunch due to undeclared milk and soy. Consumers should check product labels for the UPC 55734-00285 and contact the company for details.
Purus LabsSep 18, 2018 - Lower riskFood
Oregon Heritage Developments Inc dba Oregon Heritage Farms recalls Oregon Heritage Farms Family Blend Apple Cider, 100% Juice, 1 gallon plastic container, UPC: 8 53581 00202 0. The label
Oregon Heritage Farms recalls 1-gallon apple cider due to elevated patulin levels. Patulin is a mold byproduct that can cause health issues. Consumers should check labels for UPC 8 53581 00202 0.
Oregon Heritage FarmsSep 18, 2018 - Use cautionFood
Ozark Country Kitchen recalls Sorghum, Mfg. by Ozark Country Sorghum, Dunnegan, MO 65640, Net Wt. 2 lb. 14 OZ. packaged in glass jars
Ozark Country Kitchen recalls sorghum jars due to high nitrate levels linked to methemoglobinemia cases in Iowa. Consumers should check product labels for affected items.
Ozark Country KitchenSep 18, 2018 - Lower riskMedical device
BioMerieux SA recalls NucliSENS¿ Magnetic Extraction Reagents
BioMerieux recalls NucliSENS Magnetic Extraction Reagents from specific lots due to potential performance issues from low temperatures. Affected units may not function correctly if stored in cold environments.
BioMerieuxSep 17, 2018 - Use cautionMedical device
Leica Microsystems, Inc. recalls BOND Slide Labeler Zebra Printer Model TLP3842 and Model GX4301, for use with BOND-III and BOND-MAX instruments
Leica recalls BOND Slide Labeler Zebra Printers TLP3842 and GX4301 with faulty power supplies that may overheat and cause fire. Affected units have specific part numbers and date codes.
LeicaSep 17, 2018 - Lower riskMedical device
Medtronic Navigation, Inc.-Littleton recalls Medtronic Navigation 0-arm 02 Imaging System interventional fluoroscopic x-ray system: OARM BI70002000 SYS IMAGING 02
Medtronic Navigation recalls OARM BI70002000 SYS IMAGING 02 imaging systems for a software update to prevent potential safety issues. Affected units have serial numbers C0875 to C2012.
Medtronic NavigationSep 17, 2018 - Lower riskMedical device
Beckman Coulter Inc. recalls Kaluza C Flow Cytometry Software, RX Only in the U.S.A., Beckman Coulter, Inc. for the following software devices: (A)
Beckman Coulter recalls Kaluza C Flow Cytometry Software due to compatibility issues with Windows 7, 8, and 10 updates causing reporting delays.
Beckman CoulterSep 17, 2018 - Lower riskMedical device
Sterilmed, Inc. recalls Reprocessed Agilis Steerable Introducer: indicated for introducing various cardiovascular catheters into the heart. (a)
Sterilmed recalls reprocessed Agilis Steerable Introducers that may not meet endotoxin requirements per product specifications. Affected units have specific product codes and expiration dates prior to June 8, 2019.
SterilmedSep 17, 2018 - Lower riskDrug
Medline Industries Inc recalls SparkleFresh Fluoride Toothpaste, Sodium Monofluorophosphate 0.76%, a) 17 g tube (NDC 53329-083-92, product number
Medline recalls SparkleFresh Fluoride Toothpaste due to microbial contamination in non-sterile product. Affected tubes include 17g, 24g, and 42.5g sizes with specific lot numbers and expiration dates.
MedlineSep 17, 2018 - Lower riskDrug
Otsuka Pharmaceutical Development & Commercialization, Inc. recalls treatNOW ABILIFY (aripiprazole) / ABILIFY MAINTENA 400-mg (aripiprazole) for extended release injectable suspension.
Otsuka recalls physician sample kits of ABILIFY (aripiprazole) due to mislabeling. Product name misspelled, storage instructions missing, and contents incorrectly labeled. Consumers should check kit details and contact Otsuka for guidance.
OtsukaSep 17, 2018 - Lower riskDrug
Endo Pharmaceuticals, Inc. recalls robaxin-750 (methocarbamol tablets, USP), 750 mg, 100-count bottle, Rx Only, Distributed by: Endo Pharmaceuticals Inc.,
Endo Pharmaceuticals recalls Robaxin 750mg tablets due to incorrect dosage instructions on labels. This could lead to unsafe dosing if users follow the wrong label instructions.
Endo PharmaceuticalsSep 17, 2018 - Use cautionVehicle
MAZDA MAZDA6 (2010) recall — Suspension
Mazda recalls 2009-2010 Mazda6 vehicles with corrosion risk in front cross member that may cause steering misalignment and crash. Owners must contact Mazda by March 18, 2019 for free repair.
MazdaSep 14, 2018 - Use cautionVehicle
MITSUBISHI OUTLANDER SPORT (2018) recall — Forward Collision Avoidance
Mitsubishi recalls 2018 Outlander Sport vehicles with faulty Forward Collision Avoidance software that may prevent automatic emergency braking and other safety features from working properly.
MitsubishiSep 14, 2018 - Use cautionVehicle
BENTLEY BENTAYGA (2018) recall — Back Over Prevention
Bentley recalls 2018 Bentayga models with potential rearview camera obstruction causing crash risk. Owners must reprogram infotainment software free of charge by October 19, 2018.
BentleySep 14, 2018 - Use cautionVehicle
ALFA ROMEO GIULIA (2018) recall — Electrical System
Chrysler recalls 2017-2018 Alfa Romeo Giulia and Stelvio models with 2.0L engines due to potential fire risk from overheated catalytic converters.
Alfa RomeoSep 14, 2018 - Use cautionVehicle
MITSUBISHI ECLIPSE CROSS (2019) recall — Electrical System
Mitsubishi recalls 2019 Eclipse Cross vehicles with faulty brake software that may cause unintended braking, increasing rear-end collision risk. Owners must contact MMNA for free software update.
MitsubishiSep 14, 2018 - Use cautionVehicle
GRAND DESIGN REFLECTION (2019) recall — Equipment
Grand Design is recalling 2019 Reflection travel trailers with improperly wired outdoor outlets that could cause electrical shock. Owners must have a GFI-protected outlet installed by dealers.
Grand DesignSep 14, 2018 - Use cautionVehicle
CRUISER RV FUN FINDER EXTREME LITE (2019) recall — Suspension
Cruiser RV is recalling 2019 Fun Finder Extreme Lite travel trailers due to potential hub bearing failure causing separation from axle and crash risk. Affected owners should contact customer service for free hub or axle replacement.
Cruiser RVSep 14, 2018
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