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
34,956 found- Use cautionVehicle
WINNEBAGO FORZA (2019) recall — Equipment
Winnebago recalls 2018-2019 Forza motorhomes with potential fuel leaks near ignition sources that could cause fire. Owners must have edge protection installed by dealers by January 18, 2019.
WinnebagoNov 30, 2018 - Use cautionVehicle
KEYSTONE MONTANA (2019) recall — Suspension
Keystone is recalling 2019 Montana trailers with potentially defective axle welds that could cause spindle and wheel detachment, increasing crash risk. Owners must have axle inspected by dealers.
KeystoneNov 30, 2018 - Use cautionVehicle
HEARTLAND SUNDANCE (2019) recall — Visibility
Heartland is recalling 2019 Sundance trailers with missing reflectors that could reduce visibility to other drivers, increasing crash risk. Owners must contact Heartland by Dec 26, 2018 for free reflector installation.
HeartlandNov 30, 2018 - Use cautionMedical device
Beaver Visitec recalls BVI Visitec Soft Tip Cannula, 0.8MM .50 x 33mm (25G x 1.3 in). The BVI Soft Tip Cannula is intended to irrigate and/or
Beaver Visitec recalls specific lots of Soft Tip Cannula for potential eye injury if the silicone tip breaks off during use. Affected lots include 60047S4, 60060S9, and 600623S.
Beaver VisitecNov 30, 2018 - UnratedMedical device
Siemens Medical Solutions USA, Inc. recalls Siemens Biograph Horizon PET/CT System, Product Usage: The Siemens Biograph systems are combined X-Ray Computed
Siemens recalls specific models of Biograph Horizon PET/CT scanners due to improper design specifications. Affected units have serial numbers listed in the recall notice. Consumers should contact Siemens for details.
SiemensNov 30, 2018 - Use cautionMedical device
GE Healthcare, LLC recalls System, Tomography Computed Emmission
GE Healthcare recalls specific nuclear medicine systems with outdated software that caused a patient finger injury during the Unload process. Affected models include ASM001605, H3000YT, H3000YW, H3000YY, H3000ZW. Update software to prevent injury.
GE HealthcareNov 30, 2018 - Lower riskMedical device
Philips Medical Systems Nederlands recalls Azurion lnterventional Fluoroscopic X-ray System, with software version 1.2
Philips recalls Azurion interventional fluoroscopy systems with software version 1.2 due to potential radiation emissions too low for diagnostic images. Affected units may need software update.
Philips Medical SystemsNov 30, 2018 - UnratedMedical device
Tosoh Bioscience Inc recalls ST AIA-PACK ACTH (ACTH: Adrenocorticotropic Hormone) is designed for IN VITRO DIAGNOSTIC USE ONLY for the quantitative
Tosoh Bioscience recalls ST AIA-PACK ACTH diagnostic kits for accurate ACTH measurement. This in vitro diagnostic product is used for adrenal gland disorders. All lots are affected.
Tosoh BioscienceNov 30, 2018 - UnratedDrug
VistaPharm, Inc. recalls NYSTATIN Oral Suspension, USP 500,000 Units/5mL, unit dose 5ml cups, packaged in a) 50 unit dose cups (10x5ml unit dose
VistaPharm recalls NYSTATIN Oral Suspension due to impurities failing quality specifications. This medication is for prescription use only and may pose health risks if consumed.
VistaPharmNov 30, 2018 - UnratedDrug
Aurobindo Pharma USA Inc. recalls Amlodipine and Olmesartan Medoxomil Tablets, 5 mg/40 mg, Rx only, 30-count bottle, Distributed by: Aurobindo Pharma
Aurobindo Pharma recalls 5mg/40mg Amlodipine and Olmesartan Medoxomil tablets that were pink instead of cream. This is a pharmacist-reported discoloration issue for prescription use.
Aurobindo PharmaNov 30, 2018 - Stop using nowFood
K & T Oriental Imports Inc. recalls Salmon fillets packaged inside Styrofoam boxes fully surrounded and covered in ice, which were stored inside a
K & T Oriental Imports recalls salmon fillets in Styrofoam boxes with ice that may be contaminated with Listeria monocytogenes. Products from lot 7227-7228, produced 11/8/2018, should be discarded.
K & T Oriental ImportsNov 30, 2018 - Use cautionVehicle
MERCEDES-BENZ METRIS (2017) recall — Fuel System, Gasoline
Daimler Vans USA recalls 2016-2017 Mercedes-Benz Metris vehicles with a potential fuel leak that could cause fire if an ignition source is present. Owners must have the affected hose replaced free of charge by dealers starting January 25, 2019.
Mercedes-BenzNov 29, 2018 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Sensis Vibe System, Model Number 11007642, with software version VD10B.
Siemens recalls Sensis Vibe System model 11007642 with software VD10B due to potential system crashes during ablation procedures. Affected units must restart before continuing clinical work or use alternative systems.
SiemensNov 29, 2018 - Lower riskMedical device
Ortho Clinical Diagnostics Inc recalls Vitros Myoglobin Calibrators, Product Code 6801043 For use in the calibration of the VITROS ECi/ECiQ Immunodiagnostic
Ortho Clinical Diagnostics recalls Vitros Myoglobin Calibrators (Product Code 6801043) due to potential calibration failures or atypical quality control results after successful calibration. Affected lots 1271-1310 (expired) and 1315+ (in-date) for VITROS ECi/ECiQ, 3600, and 5600 systems.
Ortho Clinical DiagnosticsNov 29, 2018 - Use cautionMedical device
OMNIlife science Inc. recalls OMNI K1 Broach Handle, Product Code HS-10054
OMNIlife recalls OMNI K1 Broach Handle (Product Code HS-10054) due to potential inner pin loosening and falling out. Affected units sold with Lot Number MM0118.
OMNIlifeNov 29, 2018 - Lower riskDrug
Advanced Pharma Inc. recalls Phenylephrine HCl, 1 mg in Sterile Water for Injection, QS 10mL Injectable Solution, 1 mg/10 mL incorrectly labeled as
Advanced Pharma recalls Phenylephrine HCl 1mg in Sterile Water for Injection, 10mL solution due to incorrect labeling of concentration. This error could lead to improper dosing if used without proper understanding.
Advanced PharmaNov 29, 2018 - Use cautionVehicle
PORSCHE PANAMERA (2018) recall — Service Brakes, Hydraulic
Porsche recalls 2018 Panamera models with corroded brake lines that could reduce braking ability and increase crash risk. Owners must have brake lines replaced free by dealers.
PorscheNov 28, 2018 - Use cautionVehicle
PORSCHE CAYENNE (2018) recall — Equipment
Porsche recalls 2018 Cayenne models with optional ski bags due to potential strap failure in crashes. Owners must return ski bags for free replacement to prevent injury risk.
PorscheNov 28, 2018 - Use cautionVehicle
FORD FOCUS (2018) recall — Power Train
Ford recalls 2016-2018 Focus vehicles with 1.0L Fox GTDI engine and 6-speed manual transmission due to potential transmission fluid leak causing fire if near ignition sources.
FordNov 28, 2018 - Use cautionVehicle
KEYSTONE OUTBACK (2019) recall — Power Train
Keystone is recalling 2019 Outback trailers with potentially overheating hub bearings that could cause handling issues and crash risk. Owners must contact customer service for free repairs.
KeystoneNov 28, 2018 - Use cautionVehicle
HONDA RIDGELINE (2019) recall — Structure
Honda recalls 2019 Ridgeline vehicles with potential curtain air bag deployment issues during crashes. The recall addresses a risk of injury from improper center pillar trim panel alignment.
HondaNov 28, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Maximum Variable Pitch Compression Screw Caddy, Reference Number 231201003 Product Usage: Intended to carry implants
Zimmer Biomet recalls specific caddy models for potential silicone shedding during cleaning and sterilization. Affected units include lot numbers 453392 to 512868. Consumers should contact the company for details.
Zimmer BiometNov 28, 2018 - Use cautionMedical device
Howmedica Osteonics Corp. recalls Tritanium Posterior Lumbar (PL) cage intervertebral body fusion implant. Intended for an open, less invasive, and
Howmedica recalls Tritanium Posterior Lumbar cage implants due to reports of fractures during and after surgery. Affected models include specific lot numbers and model numbers listed in the recall notice.
HowmedicaNov 28, 2018 - UnratedMedical device
Implant Direct Sybron Manufacturing, LLC recalls ImplantDirect InterActive Precision IO Scan Adapter, Part #6530-09PT, Platform: 3.0mm, Non-Sterile, Rx. The firm name
Implant Direct recalls a specific precision IO scan adapter (part #6530-09PT) due to a loose component that could fall into a patient's mouth during procedures, causing aspiration or ingestion.
Implant DirectNov 28, 2018 - Lower riskMedical device
Boston Scientific Corporation recalls IntellaNav MiFi Open-Irrigated Ablation Catheter Product Usage: Open Irrigated ablation catheters, when used with a
Boston Scientific recalls IntellaNav MiFi Open-Irrigated Ablation Catheters due to unapproved resin material changes that may not be reflected in product documentation. Affected units include specific batch numbers with expiration dates.
Boston ScientificNov 28, 2018 - Lower riskFood
Frutarom USA Inc. recalls Sebastiano's Naturally Flavored Gourmet Syrups Hazelnut 25.4 fl oz (750 ml)
Sebastiano's Naturally Flavored Gourmet Syrups Hazelnut 25.4 fl oz (750 ml) recalled due to hazelnuts not being declared in ingredient statements. Consumers should check product codes listed.
Sebastiano'sNov 28, 2018 - Use cautionVehicle
TOYOTA HIGHLANDER (2018) recall — Electrical System
Wanda recalls aftermarket windshields for 2014-2018 Toyota Highlanders. Water leaks into wire harness may damage engine control module, causing engine stalling and crash risk. Free inspection and replacement.
WandaNov 27, 2018 - Use cautionVehicle
DUCATI PANIGALE V4 (2018) recall — Engine And Engine Cooling
Ducati is recalling 2018-2019 Panigale V4 motorcycles due to potential oil cooler cracks causing leaks that may increase crash risk. Owners should contact customer service for free replacement.
DucatiNov 27, 2018 - Use cautionVehicle
AUDI A5 (2018) recall — Air Bags
Volkswagen recalls 2018 Audi A5 Sportbacks with potentially faulty air bag mounting screws that could cause injury if air bags don't deploy correctly during crashes.
AudiNov 27, 2018 - Use cautionVehicle
MERCEDES-BENZ GLC350E (2019) recall — Air Bags
Mercedes-Benz recalls 2019 GLC350E vehicles with audio head units that may incorrectly show passenger air bags as 'ON' when they are not, increasing crash injury risk. Owners must contact MBUSA for free software update.
Mercedes-BenzNov 27, 2018
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