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 riskFood
Jarrow Formulas Inc recalls Jarrow Formulas Liquid L-Carnitine; 16 fl oz. (475 ml) bottle, dietary supplement; product number 102006; UPC 7 90011
Jarrow Formulas recalls 16 fl oz L-Carnitine supplements with a higher than normal micro result at six months. This dietary supplement may pose a risk for some users. Check product details to see if you have the affected batch.
Jarrow FormulasJan 15, 2018 - Use cautionMedical device
NeuroLogica Corporation recalls Solid state x-ray imager (flat panel/digital imager) Solid state x-ray imager (flat panel/digital imager) Medical
NeuroLogica recalls medical flat panel digital x-ray imagers (model GMR40, serials 00001-00016) due to potential foot injury during backward transport of retrofit equipment.
NeuroLogicaJan 12, 2018 - Lower riskMedical device
Tecan US, Inc. recalls Cortisol Saliva Luminescence Immunoassay The IBL International Cortisol Saliva Luminescence immunoassay is intended for
Tecan recalls Cortisol Saliva Luminescence Immunoassay kits that may produce 1.3-1.8x higher cortisol readings than NIST standard, affecting adrenal disorder diagnosis.
TecanJan 12, 2018 - Use cautionMedical device
Hill-Rom, Inc. recalls Progressa Bed - AC-powered adjustable hospital bed
Hill-Rom recalls AC-powered adjustable hospital beds from June 2017 due to brake system failure risk. Affected models S159AW9192 to S305AW2321 may cause bed movement and patient injury if brakes malfunction.
Hill-RomJan 12, 2018 - Lower riskMedical device
Alcon Research, LTD. recalls Alcon 25+¿ TOT ALPLUS¿ Vitrectomv Pak Includes all necessary items for a core vitrectomy procedure and connects to the
Alcon recalls specific lot (2060953H) of 25+ TOTALPLUS Vitrectomy Paks due to potential inclusion of 23GA ULTRAVIT probe instead of 25GA ULTRAVIT probe.
AlconJan 12, 2018 - Lower riskMedical device
Shimadzu Medical Systems recalls Sonialvision Safire II, Model #: DAR-8000f Product Usage: This angiographic x-ray system device intended to be used for
Shimadzu Medical Systems recalls Sonialvision Safire II angiographic x-ray systems (DAR-8000f) due to potential reset of irradiation time and integral dose readings when using specific pulse rates, with one reported incident.
Shimadzu Medical SystemsJan 12, 2018 - Lower riskMedical device
Beckman Coulter Inc. recalls 1) Cytomics FC 500 With CXP Software BECKMAN COULTER 2) Cytomics FC 500 MPL With MXP Software BECKMAN COULTER flow
Beckman Coulter recalls FC 500 flow cytometers with potential signal loss causing inaccurate patient results. Affected models include CXP and MXP software versions from 2002-2018.
Beckman CoulterJan 12, 2018 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Artis one fluoroscopic x-ray system and patient table Artis one is an angiography system developed for diagnostic
Siemens recalls Artis One fluoroscopy systems with missing or incorrectly installed snap rings that could cause tabletop carriage to slide to floor. Affected units have specific serial numbers.
SiemensJan 12, 2018 - Lower riskMedical device
Cook Inc. recalls MINC Benchtop Incubator (Mini Incubator) catalog (K-MINC-1000) G20079 is a microprocessor controlled, gassed,
Cook Inc. recalls MINC Benchtop Incubators due to potential temperature fluctuations in incubation lids that could affect cell culture results. Affected units may need repair or replacement.
Cook Inc.Jan 12, 2018 - Lower riskMedical device
Medline Industries, Inc. recalls BARD MYPICC Kit, REF CK000095B, 5F French Size, packaged 5 kits/case, Sterile, RX, For use in vascular access
Medline recalls BARD MYPICC Kit (REF CK000095B) due to potential unsterilized cases. This affects vascular access kits sold between 2018-2019. Contact Medline for details.
MedlineJan 12, 2018 - Lower riskMedical device
Howmedica Osteonics Corp. recalls Knee Prosthesis, Sterile, Single-Use devices Product Usage: The knee system devices are intended for use in revision
Howmedica recalls knee prosthesis devices that may contain incorrect implant sizes. This affects revision total knee arthroplasty procedures. Consumers should check product lot codes.
HowmedicaJan 12, 2018 - Use cautionDrug
International Laboratories, Inc. recalls Pravastatin Sodium Tablets, USP, 10 mg, 30-count bottles, packaged in 12 x 30 tablets for individual patient dispensing
International Laboratories recalls Pravastatin Sodium 10mg tablets due to potential foreign 20mg tablets. Check lot 117093A.
International LaboratoriesJan 12, 2018 - Stop using nowDrug
AuroMedics Pharma LLC recalls Levofloxacin in 5% Dextrose Injection, 250 mg/50 mL (5 mg/mL), 50 mL Single-Use flexible container, Rx Only,
AuroMedics Pharma recalls levofloxacin injection with visible mold particles. Stop using if you have this specific product. Contact for details.
AuroMedicsJan 12, 2018 - Lower riskDrug
The Compounding Pharmacy of America recalls HCG 5,000 IU/mL + Methylcobalamin 500 mcg/mL Injection 5 mL, Multi-Dose Vial, Sterile, Rx Only, Compounded by The
The Compounding Pharmacy of America recalls HCG 5,000 IU/mL + Methylcobalamin 500 mcg/mL Injection 5 mL vials due to non-sterility. This poses a risk of infection from improper sterility.
The Compounding Pharmacy of AmericaJan 12, 2018 - Stop using nowFood
Gobugi Holdings Inc recalls Dried Anchovy, size (S), (M), (L), packaged in 1.5 kg. cardboard box without brand name. The cardboard box states
Gobugi Holdings recalls dried anchovies (S, M, L) due to potential Clostridium botulinum contamination. Products sold in 1.5kg cardboard boxes without brand names. Consumers should check UPCs and contact the company for details.
Gobugi HoldingsJan 12, 2018 - Stop using nowFood
Whole Food Market recalls Cheesecake Bars, PLU number 240801, 2 oz. UPC: 0240801001992
Whole Food Market recalls specific batches of 2 oz. Cheesecake Bars due to undeclared almond flour, posing an allergy risk in CT, MA, and RI.
Whole Food MarketJan 12, 2018 - Use cautionFood
Manicaretti Inc recalls IASA COLATURA DI ALICI DI CETARA ANCHOVY EXTRACT; 100 ml and 250 ml sizes; UPC 100 ml - 7 93232 54200 3; UPC 250 ml - 7
Manicaretti Inc recalls IASA Colatura di Alici anchovy extract (100ml/250ml) due to high histamine levels. Check your UPC and expiration date.
ManicarettiJan 12, 2018 - Stop using nowFood
Brolite Products Inc recalls BROLITE PRODUCT #6109 BREAD FLAVOR R, Net Wt. 50 Lbs
Brolite Products Inc is recalling Bread Flavor R yeast due to potential metal fragment contamination. Check lot codes and manufacturing dates for affected batches.
Brolite ProductsJan 12, 2018 - Stop using nowConsumer product
Coldwater Creek Recalls Snow Globes Due to Fire Hazard (Recall Alert)
Coldwater Creek recalls two snow globe styles due to fire risk from light refraction. Stop using and return for refund.
Coldwater CreekJan 12, 2018 - Use cautionVehicle
LINCOLN MKZ (2012) recall — Air Bags
Ford is recalling 2012 Lincoln MKZ vehicles with defective passenger air bags that may not inflate properly during crashes, increasing injury risk. Owners must contact Ford for free replacement.
FordJan 11, 2018 - Use cautionVehicle
SUBARU IMPREZA (2014) recall — Engine And Engine Cooling
Subaru recalls 2014 Impreza models with potential engine stall causing crash risk. Owners must contact Subaru for free valve spring replacement.
SubaruJan 11, 2018 - Use cautionVehicle
SUBARU LEGACY (2018) recall — Electrical System
Subaru is recalling 2018 Legacy vehicles with inaccurate fuel displays that may cause unexpected stalling and crashes. Owners will receive free software updates to fix the issue.
SubaruJan 11, 2018 - Use cautionVehicle
MACK ANTHEM (AN) (2019) recall — Steering
Mack is recalling 2019 Anthem vehicles due to potential steering shaft separation causing loss of steering. Owners should contact Mack for free inspection and correction.
MackJan 11, 2018 - Use cautionVehicle
BUICK ENCORE (2019) recall — Air Bags
General Motors recalls 2019 Buick Encore vehicles with air bags that may not deploy in crashes. Owners must contact GM for free reprogramming of the SDM module.
BuickJan 11, 2018 - Use cautionVehicle
ACURA MDX (2019) recall — Service Brakes, Hydraulic
Honda recalls 2017-2019 Acura MDX models with potential brake performance issues. The recall addresses reduced braking due to gas pockets in brake calipers, requiring free brake bleeding at dealerships.
HondaJan 11, 2018 - Lower riskMedical device
GE Medical Systems Information Technologies, Inc. recalls GE HEALTHCARE CARESCAPE Central Station (CSCS) software version 2.0.2 The CARESCAPE Central Station is intended to
GE Healthcare recalls CARESCAPE Central Station software version 2.0.2 units that may experience unexpected NO COMM (No Communication) and network communication issues after boot-up or system restart. Affected units have specific model numbers and serial numbers listed in the recall.
GE HealthcareJan 11, 2018 - Lower riskMedical device
TriMed Inc. recalls Hex Driver Part Number HXDRIVER-2.0 AO; Hex Driver Part Number HXDRIVR-2.5 AO; Hex Driver Part Number HXDRIVR-2.5CL AO;
TriMed recalls specific Hex Driver models due to epoxy band migration after sterilization cycles, potentially contaminating trays. Affected units include HXDRIVER-2.0 AO, HXDRIVR-2.5 AO, and others with listed lot numbers.
TriMedJan 11, 2018 - Lower riskMedical device
Ellex iScience, Inc. recalls ellex I.Science iTRACK 250A, Canaloplasty Microcatheter Kit, for single use, REF iT-250A, Rx. The firm name on the
Ellex iScience recalls iTRACK 250A Canaloplasty Microcatheter Kits (REF iT-250A) due to sterility failure in one unit. Affected kits were sold with lot number 1711-08, expiring 11/1/2019. Contact for return instructions.
Ellex iScienceJan 11, 2018 - Lower riskMedical device
Clinical Diagnostic Systems recalls VITROS Immunodiagnostic Products TSH Reagent Pack
Clinical Diagnostic Systems recalls VITROS TSH reagent packs with specific lots due to higher than expected calibrator signals causing calibration issues. Affected lots expired by May 2018.
Clinical Diagnostic SystemsJan 11, 2018 - Lower riskMedical device
Philips Medical Systems (Cleveland) Inc recalls IQon Spectral CT with 4.7.2 software version.- Model 728332, a Philips Computed Tomography X-Ray System
Philips recalls IQon Spectral CT scanners with 4.7.2 software version due to potential misrepresentation of CT images or inability to generate images. Affected units have specific serial numbers.
PhilipsJan 11, 2018
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