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
34,939 found- Use cautionVehicle
NEWMAR MOUNTAIN AIRE (2018) recall — Equipment
Newmar is recalling 2018 Mountain Aire motorhomes due to risk of slide-out rooms moving unexpectedly when ignition is off and battery disconnect is engaged, potentially causing injury.
NewmarJun 28, 2018 - Use cautionVehicle
CADILLAC CT6 (2018) recall — Seats
General Motors recalls 2016-2018 Cadillac CT6 vehicles with child seat anchorage bars that may have excess adhesive, causing injury risk if child seat doesn't attach properly.
CadillacJun 28, 2018 - Use cautionVehicle
BMW X5 (2018) recall — Suspension
BMW is recalling 2018 X5 models with potentially unsafe lower control arms that could break, increasing crash risk. Owners must have control arms inspected and replaced free by dealers.
BMWJun 28, 2018 - Use cautionMedical device
Datex-Ohmeda, Inc. recalls The Neonatal Flow Sensor Cable used on devices CARESCAPE R860, ENGSTROM CARESTATION, ENGSTROM PRO and contained in
Datex-Ohmeda recalls neonatal flow sensor cables for CARESCAPE R860 and ENGSTROM devices due to missing connector housing exposing wires. Affected units have specific serial numbers and model numbers.
Datex-OhmedaJun 28, 2018 - Use cautionMedical device
Bayer Medical Care, Inc. recalls Overhead Counterpoise Systems (OCS) OCS CONF an accessory device for use with Bayer injector systems as a support for
Bayer Medical Care recalls overhead counterpo: OCS CONF models with potential bolt overtightening that could cause system disengagement and injury. Affected units have specific serial numbers and catalog codes.
Bayer Medical CareJun 28, 2018 - Lower riskMedical device
Envoy Medical Corporation recalls Final Pack, Esteem II, Sound Processor Model 2001, containing 2 Sterile Wipes 002866-001 (which expired in April 2018).
Envoy Medical recalls Esteem II Sound Processors with expired sterile wipes. The wipes expired before their labeled date, posing a risk of infection. Consumers should check product details and contact Envoy for guidance.
Envoy MedicalJun 28, 2018 - Lower riskDrug
LUPIN SOMERSET recalls Nitrofurantoin Oral Suspension USP, 25mg/5mL, 230 mL Bottle, Rx Only, Manufactured by: Novel Laboratories, Inc.
Lupin Somerset recalls 230mL Nitrofurantoin Oral Suspension due to subpotent drug and failed content uniformity. This may not provide effective treatment for urinary tract infections. Consumers should contact the manufacturer for details.
Lupin SomersetJun 28, 2018 - Stop using nowDrug
PFIZER recalls Daptomycin for Injection, 500 mg per vial, packaged as 1 Single-dose vial per carton, Rx only, Hospira, Inc., Lake
Pfizer recalls Daptomycin 500mg injection vials with microbial contamination risks. Affected lots expire through January 2020. Stop using if you have these specific lots.
PfizerJun 28, 2018 - Lower riskFood
Bengard Ranch recalls Fresh Cilantro: Boxed by Sabor Farms, Salinas, CA 60 bunches of cilantro per box
Bengard Ranch recalls 60 bunches of fresh cilantro from Sabor Farms in Salinas, CA due to Salmonella contamination found in FDA samples. Consumers should check lot numbers and use by dates.
Bengard RanchJun 28, 2018 - Lower riskFood
Pinnacle Food Group, Llc recalls Wish Bone House Italian Salad Dressing 15 oz.
Pinnacle Food Group recalls Wish Bone House Italian Salad Dressing 15 oz. due to unlabeled milk and egg ingredients. Consumers should check product labels for the case lot code 4913019S51.
Pinnacle Food GroupJun 28, 2018 - Use cautionVehicle
FOREST RIVER SALEM (2019) recall — Equipment
Forest River is recalling 2016-2019 Salem trailers due to water heater exhaust panel covered by shower faucet when opened, increasing injury risk. Owners can get free replacement shower panel.
Forest RiverJun 27, 2018 - Use cautionMedical device
Ion Beam Applications S.A. recalls Proteus 235, Universal Nozzle with snout 300x400; PBS dedicated nozzle with snout XL Product Usage: Device is designed
Ion Beam Applications recalls Proteus 235 proton therapy devices due to risk of patient or user injury from improper nozzle alignment during treatment. Affected units may cause crushing or mistreatment if apertures aren't correctly positioned.
Ion Beam ApplicationsJun 27, 2018 - Lower riskMedical device
Stryker GmbH recalls Stryker T2 ANKLE ARTHRODESIS NAIL RIGHT 10MMX200MM Item Number: 1819-1020S T2 ANKLE ARTHRODESIS NAIL RIGHT 12MMX200MM
Stryker recalls specific ankle and humeral nail models due to potential sterility compromise from incomplete Tyvek lid seals. Affected items include right 10mm/200mm and 12mm/200mm ankle nails, and certain humeral nails. Contact Stryker for details.
StrykerJun 27, 2018 - Lower riskMedical device
Genicon, Inc. recalls Genicon EZee Single Use Specimen Retrieval Bag - Product Usage: This device is disposable and is packaged and
Genicon recalls disposable specimen retrieval bags that may be used for multiple specimens, risking contamination. Affected units include model 550-000-00:000 with lot I8920 from August 2020.
GeniconJun 27, 2018 - Lower riskMedical device
Elekta Instrument AB recalls Leksell GammaPlan 11.1 Product Usage: Leksell GammaPlan is a computer-based system designed for Leksell Gamma Knife
Elekta recalls Leksell GammaPlan 11.1 software due to systematic margin overestimation in certain treatment areas. Users should contact Elekta for updates.
ElektaJun 27, 2018 - Lower riskMedical device
bioMerieux, Inc. recalls BACT/ALERT VIRTUO system, B Unit, with Version R2.0 Firmware Product Usage: The BacT/ALERT VIRTU Microbial Detection
Biomerieux recalls BACT/ALERT VIRTUO system B Units with R2.0 firmware due to potential calibration issues. Affected units may show anomalies if calibration standards aren't properly repositioned during service. Contact for remedy details.
BiomerieuxJun 27, 2018 - Stop using nowMedical device
Philips Medical Systems Gmbh, DMC recalls BuckyDiagnost Ceiling System (Stitching Patient Support) 704031
Philips recalls BuckyDiagnost Ceiling System (Stitching Patient Support) 704031 due to footplate falling risk. Affected units have serial numbers starting with 477195/SN110: stop using immediately.
Philips Medical SystemsJun 27, 2018 - UnratedDrug
Aidarex Pharmaceuticals LLC recalls Enalapril Maleate, USP 5MG, 30-count bottle, RX only. Packaged By: Aidarex Pharmaceuticals. Mfg: Wockhardt Ltd. India.
Aidarex Pharmaceuticals recalls 5mg enalapril maleate bottles due to potential degradation products affecting safety. This recall applies to specific lot numbers and expiration dates.
Aidarex PharmaceuticalsJun 27, 2018 - Use cautionMeat & poultry
Aunt Kitty's Foods Inc. Recalls Canned Chicken Products Due to Possible Processing Deviation
USDA FSIS recalls 10,805 pounds of canned chicken gravy products from Aunt Kitty's Foods Inc. due to possible underprocessing. Consumers are urged not to consume these products.
Aunt Kitty's FoodsJun 26, 2018 - Lower riskMedical device
Encore Medical, Lp recalls Instrument trays used to store AltiVate Small Shell Trials (FA S ALTIVATE RSP HUM TRLS SM). Metal container with lid
Encore Medical recalls instrument trays used in orthopedic surgery due to potential non-biocompatible black coating after cleaning. Affected units may pose health risks if used improperly.
Encore MedicalJun 26, 2018 - Lower riskMedical device
Terumo Cardiovascular Systems Corporation recalls CDI Blood parameter monitoring system 500 H/SAT, Part No. 145883 Product Usage: The CDI System 500 provides continuous,
Terumo recalls CDI Blood parameter monitoring system 500 H/SAT with Part No. 145883 due to Color Chip Test failures that disable the H/Sat module. No device inaccuracy occurs.
TerumoJun 26, 2018 - UnratedDrug
World Organix, LLC recalls Blissful Remedies Red Maeng Da, 100% Mitragyna Speciosa capsule, 50-count packaged White Foil Pouche, Dist. by World
World Organix recalls some Blissful Remedies Red Maeng Da capsules due to potential microbial contamination. Products with UPC#7 22589 32355 3 and Lot Code 102710 may be unsafe.
World OrganixJun 26, 2018 - Use cautionDrug
MAJOR PHARMACEUTICALS recalls Enalapril Maleate Tablets, USP, 5 mg, 100 Tablets (10 x 10) Unit Dose per carton, Rx only, Manufactured by: Wockhardt
Major Pharmaceuticals recalls Enalapril Maleate 5mg tablets due to failed impurity specifications. Check your lot numbers and expiration dates for affected units.
Major PharmaceuticalsJun 26, 2018 - Stop using nowConsumer product
Huish Outdoors Recalls Scuba Diving Regulators Due to Drowning Hazard
Huish Outdoors recalls scuba regulators with part numbers listed that can restrict airflow at low tank pressure (below 500 psi), risking drowning. Consumers should stop using and get free repairs.
Huish OutdoorsJun 26, 2018 - Stop using nowConsumer product
Baccus Recalls Stanley Workbench LED Light and Power Stations Due to Shock and Electrocution Hazards (Recall Alert)
Baccus recalls Stanley workbench LED lights with model WLB40PS due to wiring errors causing shock and electrocution. Stop using immediately and contact for free replacement or refund.
BaccusJun 26, 2018 - Lower riskMeat & poultry
Recall Notification Report 054-2018 (Ham Products)
USDA recalls 4,944 pounds of Land O'Frost ham products due to misbranding: front labels say Black Forest Ham but back labels incorrectly list Honey Smoked Turkey Breast.
Land O'FrostJun 25, 2018 - Lower riskMeat & poultry
People's Sausage Co. Recalls Jerky and Meat Stick Products Produced without an Approved Voluntary Grant of Inspection
USDA recalls 13,554 pounds of jerky and meat sticks produced without approved inspection. Consumers urged not to eat these products, which should be thrown away or returned.
People's Sausage Co.Jun 25, 2018 - Use cautionVehicle
AUDI A8 (2015) recall — Fuel System, Gasoline
Volkswagen is recalling 2015 Audi A8 vehicles with a fuel leak risk that could cause fire if an ignition source is present. Owners must have the fuel line replaced free of charge by dealers.
AudiJun 25, 2018 - Use cautionVehicle
SPARTAN METROSTAR (2017) recall — Electrical System
Spartan is recalling 2017 MetroStar emergency vehicles with a faulty water pump solenoid that can cause loss of water pressure during fires, increasing injury risk. Owners must have solenoids replaced free by August 7, 2018.
SpartanJun 25, 2018 - Use cautionVehicle
MAZDA CX-5 (2018) recall — Air Bags
Mazda is recalling 2018 CX-5 vehicles with side curtain air bags that may not deploy properly in side impacts or rollovers, increasing injury risk. Owners should contact Mazda for free replacement.
MazdaJun 25, 2018
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