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
34,896 found- Use cautionMeat & poultry
Supermercado Selectos, San Sebasti†n, Recalls Raw, Frozen Siluriformes Fish, Meat and Poultry Products Produced Without Benefit of Inspection
USDA recalls frozen Siluriformes fish, beef, pork and poultry from Supermercado Selectos in Puerto Rico that were produced without federal inspection. Consumers are urged not to consume these products and should discard or return them.
Supermercado SelectosJun 7, 2018 - Use cautionVehicle
BMW X4 (2019) recall — Service Brakes, Hydraulic
BMW recalls certain 2019 X4 models due to potential rear brake performance issues. Owners should contact BMW for free brake circuit bleeding.
BMWJun 7, 2018 - Lower riskMedical device
GE Medical Systems, LLC recalls GE Healthcare MRI Systems, Software Version 11.x, sold under the following product names: 1.5T CXK4 LCC MAGNET,1.5T
GE Healthcare recalls MRI systems with software version 11.x due to potential image flips left/right and patient data mismatches after service activities. Affected models include 1.5T and 3.0T systems with specific serial numbers.
GE HealthcareJun 7, 2018 - Lower riskDrug
Mylan Pharmaceuticals Inc. recalls Maxzide-25 (Triamterene and hydrochlorothiazide) tablets, USP, 37.5 mg/ 25 mg, 100-count bottle, Rx only, Mylan
Mylan recalls 100-count Maxzide-25 tablets (37.5mg/25mg) due to slightly elevated drug levels in routine testing. This may cause higher than intended drug effects.
MylanJun 7, 2018 - Use cautionVehicle
VOLKSWAGEN TIGUAN (2018) recall — Air Bags
Volkswagen is recalling 2018 Tiguan vehicles with a passenger air bag that may tear or not deploy correctly in crashes, increasing injury risk. Owners can get free replacement air bags.
VolkswagenJun 6, 2018 - Use cautionVehicle
BMW X3 (2019) recall — Lane Departure
BMW is recalling certain 2018-2019 X3 models with lane keeping assist to prevent crashes if warning system fails to detect hands off wheel. Owners must have steering wheel inspected by dealer.
BMWJun 6, 2018 - Use cautionMedical device
RAYSEARCH LABORATORIES AB recalls RayStation Radiation Therapy Treatment Planning System, Model nos. 2.5, 3.5, 4.0, 4.3, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1,
RaySearch recalls specific versions of RayStation radiation therapy software due to potential incorrect dose calculations in large or off-axis radiation fields, requiring validation with Beam 3D Modeling.
RaySearchJun 6, 2018 - Use cautionMedical device
Tosoh Bioscience Inc recalls G8 Automated HPLC Analyzer: HLC-723G8-ST, 021560; and HLC-723G8-LA, 021674 Product Usage: The Tosoh Automated
Tosoh recalls HLC-723G8-ST and HLC-723G8-LA analyzers with software version 5.23. HbAE can cause invalid diabetes test results if Flag 43 isn't enabled. Users should check software settings to avoid inaccurate readings.
TosohJun 6, 2018 - Use cautionMedical device
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls Single Chamber Temporary External Pacemaker, Model 53401
Medtronic recalls Model 53401 Single Chamber Temporary External Pacemakers with specific serial numbers due to potential power reset causing setting reversion during patient use.
MedtronicJun 6, 2018 - Use cautionMedical device
GE Medical Systems, LLC recalls Discovery MR750w Nuclear Magnetic Resonance Imaging System labeled as the following product name sold under: Product
GE Medical Systems recalls Discovery MR750w MRI systems with a warm bore surface that can cause serious burns if patient touches it without proper padding. Affected models include 3.0T MR750W variants with specific serial numbers. Contact GE for details.
GE Medical SystemsJun 6, 2018 - UnratedDrug
Pharmalucence, Inc. recalls Kit for the Preparation of Technetium Tc99m Medronate, 20mg in 10 mL vial, packaged in a) 5-count box (NDC
Pharmalucence recalls 5-count and 30-count boxes of Technetium Tc99m Medronate kits due to reported sterility breach. This could lead to infections if used improperly.
PharmalucenceJun 6, 2018 - Use cautionFood
Tilgner's Alaskan Salmon recalls Canoodles (ACN) coarse ground cold smoked dehydrated shelf stable sockeye salmon pieces
Tilgner's Alaskan Salmon recalls coarse ground cold smoked dehydrated sockeye salmon pieces due to potential Listeria monocytogenes contamination. Consumers should check product codes and contact the company for details.
Tilgner's Alaskan SalmonJun 6, 2018 - Lower riskFood
House Of Spices Orlando recalls LAXMI Corn Flour Fine Net Wt./Poids Net. 2LB (907g) Distributed by: House of Spices (India) Inc.
House Of Spices recalls LAXMI Corn Flour (2lb) due to high aflatoxin levels. This mold contaminant can cause serious health issues if consumed. Consumers should check product lot numbers and contact the company for details.
House Of SpicesJun 6, 2018 - Stop using nowConsumer product
Vernier Software & Technology Recalls Circuit Boards Due to Burn Hazard (Recall Alert)
Vernier is recalling Circuit Board 2 units due to a burn hazard. Stop using the board and return it for a free repair if you have one.
VernierJun 6, 2018 - Use cautionConsumer product
GE Lighting Recalls LED Tube Lamps Due to Shock and Electrocution Hazards; Sold Exclusively at Lowe's Stores
GE Lighting recalls 31243 LED13T8U840 LED tube lamps sold at Lowe's due to shock and electrocution hazards during installation. Consumers should stop using and contact GE for refund.
GE LightingJun 6, 2018 - UnratedMedical device
Stryker Neurovascular recalls Wingspan Stent System, Rx Only, Sterile EO, Catalog #: M003WE0250090, M003WE0300090, M003WE0350090, M003WE0400090,
Stryker is recalling Wingspan Stent System (Rx Only, Sterile EO) due to reported use-related coating damage on delivery catheter shafts. Affected units have specific catalog numbers. No remedy is stated in the recall notice.
Stryker NeurovascularJun 5, 2018 - Lower riskMedical device
Tosoh Bioscience Inc recalls Tosoh Bioscience AIA Analyte Application Manual (AAM) CD Part Number: 997027 CD contains analyte application manuals
Tosoh Bioscience recalls AIA Analyte Application Manual CD (part 997027) due to unapproved labeling. This CD contains manuals for 47 analyte reagent packs used with their AIA analyzers. Consumers should check if they own this CD and contact Tosoh for details.
Tosoh Biosc: AIA Analyte Application ManualJun 5, 2018 - UnratedDrug
PharMEDium Services, LLC recalls HYDROmorphone HCl 0.5 mg per mL in 0.9% Sodium Chloride, 1 mL Total Volume in 3 mL syringe, Rx, PharMEDium Services,
PharMEDium Services recalls specific hydro morphine syringes due to potential superpotent and subpotent risks. Affected lots expire by June 2018. Consumers should check lot numbers.
PharMEDiumJun 5, 2018 - Use cautionConsumer product
Keyera Energy Recalls to Inspect Propane Gas Due to Fire and Explosion Hazards
Keyera Energy recalls under-odorized propane gas that may not alert users to leaks, risking fire, explosion, or burns. Consumers should contact Keyera for free inspection and odorization if needed.
Keyera EnergyJun 5, 2018 - Use cautionMeat & poultry
Goodman Food Products Recalls Fully Cooked Ground Beef Products Due to Possible Foreign Matter Contamination
Goodman Food Products recalls 34,400 pounds of fully cooked ground beef products that may contain hard white plastic. Consumers should throw away or return these products to the place of purchase.
Goodman Food ProductsJun 4, 2018 - Use cautionVehicle
FOREST RIVER SURVEYOR (2018) recall — Tires
Forest River recalls 2018 Surveyor trailers with incorrect tire placards that could cause premature tire wear and crash risk. Owners must check placard details and contact customer service for a corrected version.
Forest RiverJun 4, 2018 - Use cautionMedical device
Leica Microsystems, Inc. recalls Leica Microsystems products labeled as the following: Leica M320 Microscope Systems with Article Numbers 10448419,
Leica Microsystems recalls M320 Microscope Systems with specific article numbers due to risk of screw failure that may cause optics carrier to drop. Affected units include specific serial numbers and article numbers listed in the notice.
LeicaJun 4, 2018 - Lower riskMedical device
B. Braun Medical, Inc. recalls 26-Lead Transfer Set for use with APEX¿ Compounding System, Product Catalog Number 2112550
B. Braun recalls 26-Lead Transfer Sets for APEX Compounding System with potential for incorrect valve orientation causing unintended drug mixtures. Check product catalog numbers listed.
B. BraunJun 4, 2018 - Stop using nowMedical device
Intuitive Surgical, Inc. recalls EndoWrist Suction Irrigator, Single Use Instrument. Part Number: 480299-04. An accessory to the EndoWrist Surgical
Intuitive Surgical recalls EndoWrist Suction Irrigator (Part 480299-04) due to potential silicone particle generation during surgery, which could enter patients. Affected units include specific lots and part numbers.
Intuitive SurgicalJun 4, 2018 - UnratedMedical device
Fx Solutions recalls Fx SOLUTIONS CENTERED HEAD CoCr 50x19, REF 106-5019 Product Usage: Device is designed to produce and deliver proton
Fx Solutions recalls Centered Head CoCr 50x19 models with blister breaches that could affect radiation treatment safety. Affected units include specific lot numbers sold only in the U.S. and Canada.
Fx SolutionsJun 4, 2018 - Lower riskMedical device
Richard-Allan Scientific Company recalls EZ Single Cytofunnel Brown, A78710004 Product Usage: The EZ Single Cytofunnel with Brown filter papter are intended for
Richard-Allan Scientific recalls EZ Single Cytofunnel Brown (A78710004) due to mislabeling. This affects lab equipment used with Thermo Scientific Cytospin. No action needed as it's a labeling issue, not a safety hazard.
Richard-Allan ScientificJun 4, 2018 - Lower riskMedical device
CryoLife, Inc. recalls BioGlue Spreader Tip, 12mm, Sterile, RX Only. Product Usage: BioGlue is indicated for use as an adjunct to standard
CryoLife recalls BioGlue Spreader Tips due to missing Syringe Spreader Tip pouches in packaging. Affected units have model BG3510-5-J and lot 18MJX002. Consumers should check packaging for indicator label.
CryoLifeJun 4, 2018 - Use cautionMedical device
Neomed Inc recalls NeoMed Enteral Feeding Tubes with Enteral Only Connectors, French sizes 4.0Fr, 5.0Fr, 6.5Fr, 8.0Fr, and lengths 40cm,
Neomed recalls enteral feeding tubes with enteral only connectors (French sizes 4.0Fr-8.0Fr) due to potential for tethered plug to open after closure. Affected units include specific model numbers and production dates.
NeomedJun 4, 2018 - Use cautionDrug
HOSPIRA INC, LAKE FOREST recalls Naloxone Hydrochloride Injection, USP, 0.4 mg/mL, 1 mL in 2.5 mL Carpuject Single-use cartridge syringe, Single unit
Hospira recalls specific naloxone injection products due to potential particulate matter on syringes, which could cause serious injury if injected. Affected products include 1 mL cartridges and 10-count boxes with certain NDC numbers.
HospiraJun 4, 2018 - Use cautionFood
Four Link Nutriworld recalls BLUEBERRY PRETZEL, NET WEIGHT : 4OZ (113g) ,USE BY DATE : 12/1/2018
Four Link Nutriworld recalls Blueberry Pretzel (4oz, use by 12/1/2018) due to missing milk allergen label. This poses a risk for milk-allergic individuals.
Four Link NutriworldJun 4, 2018
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