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
34,894 found- Lower riskMedical device
Helena Laboratories, Corp. recalls SPIFE Alkaline Hemoglobin Kit, Cat. No. 3415, for use in the separation and quantitation of hemoglobins by agarose
Helena Laboratories recalls SPIFE Alkaline Hemoglobin Kit (Cat. No. 3415) due to outdated instructions that could lead to incorrect results. Affected lots include specific 2017 and 2018 production batches with expiration dates up to December 31, 2018.
Helena LaboratoriesFeb 27, 2018 - Lower riskMedical device
Radiometer Medical ApS recalls AQURE, Software version 2.3.0 and 2.3.1 Product Usage: The AQURE system is intended to let allow the management of
Radiometer recalls AQURE software versions 2.3.0 and 2.3.1 due to potential patient mix-up. Affected healthcare facilities should update software to prevent misidentification of patient data.
RadiometerFeb 27, 2018 - Use cautionMedical device
C.R. Bard, Inc. recalls Bard(R) Premature Infant Feeding tube, ENFit(TM), REF EN0036430 Product Usage: BARD(R) Nasogastric Sump Tubes with
Bard recalls premature infant feeding tubes with ENFit connector due to potential poor fusion of tubing and connector. Affected units have specific lot numbers. Consumers should contact Bard for details.
BardFeb 27, 2018 - Lower riskFood
Ariola Foods, Inc. recalls Seviroli brand Cannoli Shells. Large Plain 36 ct., and Small Plain 72 ct.
Ariola Foods recalls Seviroli Cannoli Shells (Large Plain 36 ct. and Small Plain : undeclared soy lecithin. Consumers should check lot numbers 10008 and 18043 for affected products.
SeviroliFeb 27, 2018 - Use cautionFood
Plant Devas Inc recalls Blemish Face Care Kit; Each kit contains: Tea Tree Gel Cleanser 1 fl oz bottle Lemon Thyme Facial Tonic HydroSoul 1 fl
Plant Devas Inc recalls Evanhealy Blemish Face Care Kits due to excessive microorganisms. Check lot numbers and sell-by dates for affected units.
EvanhealyFeb 27, 2018 - Use cautionMedical device
Micro Therapeutics Inc, Dba Ev3 Neurovascular recalls MindFrame Capture LP Revascularization Devices: Product Numbers: (a) REF 300010 (b) REF 300011 (c) REF 300012 (d) REF
Micro Therapeutics recalls MindFrame Capture LP Revascularization Devices (product numbers REF 300010-300018) due to potential partial detachment from delivery wire, which could cause stroke complications.
Micro TherapeuticsFeb 26, 2018 - Use cautionMedical device
Genesee BioMedical, Inc. recalls Sternal Valve Retractors With Atrial and Aortic Rakes; Models SRCL-1, SRCL-AR, SRLP-1, SRLP-AR, ATR-1, ATR-AR, CSR-1
Genesee BioMedical recalls sternal valve retractors with atrial and aortic rakes (models SRCL-1, SRCL-AR, etc.) due to corrosion in retractor blades that may weaken welds and cause bearing failure during cardiac surgery.
Genesee BioMedicalFeb 26, 2018 - Lower riskMedical device
Preservation Solutions, Inc. recalls Cold Storage Solution, 2L, labeled as Waters IGL Cold Storage Solution, Catalog No. CSS/2000/US; and, Belzer UW Cold
Preservation Solutions recalls 2L Cold Storage Solution bags with potential small leaks at injection ports. Affected units may need replacement to prevent contamination during organ storage.
Preservation SolutionsFeb 26, 2018 - Use cautionMedical device
Beaver-Visitec International Inc. recalls WET-FIELD OSHER THERMODOT MARKER, 25GA FINE TIP, CURVED; Part number 221270. Designed to create an ink-free, fine dot
Beaver-Visitec recalls Osher Thermodot Markers with incorrect needle tips that may cause injury during medical procedures. Affected units have specific lot numbers and part numbers.
Beaver-VisitecFeb 26, 2018 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Analyzer and Atellica IM 1600 Analyzer system for in vitro diagnostic testing of clinical specimens.
Siemens Healthcare recalls Analyzer and Atellica IM 1600 systems for in vitro diagnostics due to potential inaccurate test results when multiple analyzers share a solution system. Affected units have UDI 00630414002026.
Siemens HealthcareFeb 26, 2018 - UnratedMedical device
Beaver-Visitec International Inc. recalls Wet-Field Hemostatic Eraser Bipolar 25G, fine tip, straight, 5/SP; Part Number 221267; UDI: 30886158010549
Beaver-Visitec recalls Wet-Field Hemostatic Eraser Bipolar 25G with incorrect labeling. Affected units have Part Number 221267 and UDI 30886158010549. No remedy specified in recall notice.
Beaver-VisitecFeb 26, 2018 - Lower riskDrug
Paddock Laboratories, LLC. recalls Evamist (estradiol transdermal spray), 1.53mg estradiol/spray, 0.27 fl oz (8.1 mL) per bottle, Rx Only, Manufactured
Paddock Laboratories recalls Evamist estradiol transdermal spray due to potential cracks in vial neck causing leaks and product evaporation. Rx-only product with specific lot number.
Paddock LaboratoriesFeb 26, 2018 - Lower riskDrug
Mckesson Packaging Services recalls RANITIDINE Tablets, USP 150 mg UD 100 tablets (10x10), RX Only, Manufactured by: Amneal Pharmaceuticals, Hauppauge, NY
Mckesson Packaging Services recalls 150mg RANITIDINE tablets (NDC 63739-489-10) due to failed stability specifications. These RX-only tablets, manufactured by Amneal Pharmaceuticals, may degrade over time.
Mckesson Packaging ServicesFeb 26, 2018 - Stop using nowConsumer product
Allen Sports Recalls Folding Bicycles Due to Fall Hazard
Allen Sports recalls Ultra1 and UltraX carbon folding bikes due to frame collapse risk causing falls. Affected models sold in black with 20 speeds; contact for refund.
Allen SportsFeb 26, 2018 - Use cautionVehicle
FOREST RIVER XLR TOYHAULER (2018) recall — Equipment
Forest River is recalling 2016-2018 XLR Toyhauler trailers with safety chains that don't meet weight rating, risking trailer separation and crashes. Owners must get replacement chains free.
Forest RiverFeb 23, 2018 - Lower riskMedical device
GE Healthcare recalls GE Healthcare Centricity PACS-IW, Model Numbers: (a) 2052831-00X (b) 2049588-008 Product Usage: Centricity PACS-IW by
GE Healthcare recalls Centricity PACS-IW systems with model numbers 2052831-00X and 2049588-008. A database error can cause images to be missing during exams, especially with very small image sets like a single CR Thorax image.
GE HealthcareFeb 23, 2018 - Lower riskMedical device
Sofradim Production recalls Versatex Monofilament Mesh 50 x 50cm, Product No. VTX5050M The device is made out of a macroporous three-dimensional
Sofradim recalls Versatex Monofilament Mesh 50x50cm (Product No. VTX5050M) due to reported abdominal hernia recurrence after hernia repair. Affected lots include SPC1091X through SRA2188X.
SofradimFeb 23, 2018 - Use cautionMedical device
Deerfield Imaging, Inc. recalls IMRIS ORT200 Removable Operating Room Table, 50-60 Hz Version is intended for use during diagnostic examinations or
Deerfield Imaging recalls ORT200 operating room tables with serial numbers listed. The rotational locking mechanism may fail to lock, causing unintended movement during procedures.
Deerfield ImagingFeb 23, 2018 - Lower riskMedical device
ConMed Corporation recalls MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Physio-Control¿ Quik-Combo" Connector, REF/Catalog Number 2602M
ConMed recalls Mini Infant < 3kg Radiotranslucent Electrodes with adhesive on contact wires that may impede conductivity and cause device failure. Affected units include specific lot numbers.
ConMedFeb 23, 2018 - Lower riskMedical device
Orthofix, Inc recalls ORTHOFIX, Connector System, SMALL SET SCREW, REF 79-2003
Orthofix recalls small set screws with specific lot numbers due to potential drive feature issues that could cause stripped screws. Affected items may not fit properly with the included driver.
OrthofixFeb 23, 2018 - Use cautionMedical device
Medical Components, Inc dba MedComp recalls 12F Tesio CATHETER SET (CUFF 32CM FROM TIP), REF MCTC1247SD, UDI 884908027266 Product Usage: The Medcomp Repair Kit is
MedComp recalls 12F Tesio Catheter Set (REF MCTC1247SD) due to potential connection failures causing blood loss or air emboli. Affected units have specific lot numbers and UDI.
MedCompFeb 23, 2018 - Lower riskMedical device
Civco Medical Instruments Co. Inc. recalls CIVCO lnfiniti Needle Guide Bracket. used for performing needle-guided (or catheter) procedures with the use of
Civco recalls Infinity Needle Guide Brackets due to potential cover leaks during validation testing. Affected units include specific biopsy starter kits with listed lot numbers. Consumers should contact Civco for details.
CivcoFeb 23, 2018 - Use cautionMedical device
Deerfield Imaging, Inc. recalls IMRIS ORT300, Removable Operating Room Table, Part Numbers: (a) 114093-000 (b) 114093-600
Deerfield Imaging recalls IMRIS ORT300 operating room tables with specific part numbers and serials due to potential unintended movement during use. Affected users should contact the manufacturer for details.
Deerfield ImagingFeb 23, 2018 - Lower riskMedical device
Stryker Instruments Div. of Stryker Corporation recalls T4 Zipper Toga (S/M); Catalog Number: 0400-810-000 Sterile personal protection garment
Stryker recalls sterile T4 Zipper Toga (S/M) garments with catalog number 0400-810-000 due to potential material layer separation causing contaminant exposure. Affected items may be at risk of exposure to harmful substances.
StrykerFeb 23, 2018 - UnratedDrug
Bayer HealthCare Pharmaceuticals, Inc. recalls Coppertone Kids Sunscreen Spray (avobenzone 3%, Homosalate 10%, Octisalate 5%, Octocrylene 4%, Oxybenzone 5%) 8.3 oz.
Bayer recalls 528 units of Coppertone Kids Sunscreen Spray (8.3 oz) due to a labeling mix-up. Sold in Arkansas with lots 7N04CS and 7N05CS.
CoppertoneFeb 23, 2018 - Stop using nowDrug
AstraZeneca Pharmaceuticals LP recalls Lynparza (olaparib) capsules 50 mg, 112 count bottles, Rx only, Manufactured for: Astra Zeneca Pharmaceuticals LP
AstraZeneca recalls Lynparza 50mg capsules due to impurities that could cause serious injury. Affected products have specific NDC codes and were sold between 02/2018 and 05/2018. Contact for return instructions.
AstraZenecaFeb 23, 2018 - Lower riskFood
Pinks Bakery Seattle, Inc. recalls Hippie Cookie, Marsee Baking brand, six 3.2oz cookies individually wrapped in plastic (Grab and Go) or six unwrapped,
Pinks Bakery Seattle, Inc. recalls Hippie Cookie brand six-pack cookies due to coconut not being declared in allergen statement. Consumers should check product labels for the specific batch numbers.
Hippie CookieFeb 23, 2018 - Lower riskFood
Get The Tea recalls Life Change Fat Burner, 90 Gel Caps!, Burn Fat!, Remove fat from the liver! 1000mg; 2 capsules daily
Get The Tea recalls Life Change Fat Burner capsules due to soy content. This product contains soy, which may pose health risks for some consumers.
Get The TeaFeb 23, 2018 - Lower riskFood
King of Pops recalls Key Lime Pie Handcrafted All-Natural Pop; Net Wt. 3.2 OZ (90g)
King of Pops recalls Key Lime Pie Handcrafted All-Natural Pop (3.2 oz) due to undeclared soy allergen. Consumers should check lot codes on packaging for affected items.
King of PopsFeb 23, 2018 - Lower riskFood
Gasco Industrial, Corp. recalls BELCA Soy Sauce, Contenido Neto: Un Gal¿n (128 fl. oz), Distribuido por: Mister Price Inc. San Juan, P.R. 00936
Gasco Industrial recalls BELCA Soy Sauce (128 fl oz) due to undeclared wheat allergen. Consumers should check lot numbers and contact the company for details.
Gasco IndustrialFeb 23, 2018
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