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- UnratedMedical device
Ion Beam Applications S.A. recalls Proteus 235, graphite block 8
Ion Beam Applications S.A. recalls Proteus 235 graphite block 8 due to incorrect screw hole depth. This may cause malfunction in normal use. No remedy specified.
Ion Beam Applications S.A.Oct 17, 2017 - Lower riskMedical device
Southmedic, Inc. recalls Southmedic Oxygen Masks with EtCO2 sampling line part number OM-2125-8, 25 masks per case. Minimal contact, open oxygen
Southmedic recalls oxygen masks with EtCO2 sampling line (part number OM-2125-8) due to potential loose or missing CO2 diffusers causing non-functioning. Affected units include specific model numbers and lot codes.
SouthmedicOct 17, 2017 - Lower riskMedical device
Siemens Healthcare Diagnostics recalls BC Thrombin Reagent Kit Lot Number 46751; UDI - 008427680131024675120180908 and BC Thrombin Reagent Kit Lot Number
Siemens Healthcare Diagnostics recalls two batches of Thrombin Reagent Kits that may produce unexpectedly long Thrombin Time results, potentially exceeding normal limits. Affected kits have specific lot numbers and were distributed globally.
Siemens HealthcareOct 17, 2017 - Lower riskMedical device
3M Company - Health Care Business recalls 3M Bair Hugger(TM) Normothermia System, Temperature Monitoring System Sensors Model 360 (Part Number 36000)
3M recalls Normothermia System temperature sensors that may show lower than actual patient temperatures. Affected units have specific lot numbers and expiration dates.
3MOct 17, 2017 - Use cautionMedical device
Arrow International Inc recalls Pressure Injectable Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter and Sharps Safety
Arrow recalls pressure injectable multi-lumen catheter kits with possible incorrect springwire guide. Affected kits may have safety risks. Consumers should check product codes and contact Arrow for details.
ArrowOct 17, 2017 - Lower riskDrug
Teva Pharmaceuticals USA recalls Methylphenidate Hydrochloride Tablets USP, 20 mg, 100-count bottles, Rx only, Manufactured by: Watson Laboratories,
Teva Pharmaceuticals USA recalls 20mg methylphenidate tablets due to failed dissolution testing. This may affect medication effectiveness. Contact for return instructions.
Teva PharmaceuticalsOct 17, 2017 - Lower riskFood
Stonyfield Farm recalls Stonyfield ORGANIC O'soy Strawberry on the bottom SOY YOGURT 5.3 Oz (150g), UPC Codes: 0-52159-00603-7. KEEP
Stonyfield Farm recalls organic O'soy strawberry yogurt due to potential undeclared milk. Consumers should stop using and check UPC codes 0-52159-00603-7.
Stonyfield FarmOct 17, 2017 - Lower riskFood
Weis Markets, Inc., Ice Cream Division recalls Weis, Sunbury, PA; BLT Sandwich; 1 CT
Weis Markets recalls BLT sandwiches from Sunbury, PA with undeclared egg in mayonnaise. Consumers should check product details and contact Weis for guidance.
WeisOct 17, 2017 - Stop using nowConsumer product
Target Recalls Leather Pouf Ottoman Due to Suffocation and Choking Hazards
Target recalls leather pouf ottomans with polystyrene beads that can be opened by children, causing suffocation or choking. Consumers should stop using and return for refund.
TargetOct 17, 2017 - Stop using nowConsumer product
Polaris Recalls ACE 325 Recreational Off-Highway Vehicles Due to Fire and Burn Hazards
Polaris recalls 2014-2016 ACE 325 ATVs due to exhaust pipe cracks causing fire and burn hazards. Owners must stop using and contact Polaris for free repairs.
PolarisOct 17, 2017 - Stop using nowConsumer product
Herman Miller Recalls Fiberglass Rocking Chairs Due to Fall Hazard
Herman Miller recalls Eames fiberglass rockers with model numbers starting RFAR due to risk of base separation causing falls. Consumers must stop using and return for full refund.
Herman MillerOct 17, 2017 - Stop using nowConsumer product
Frontier Wood Chippers Recalled by John Deere Due to Injury Hazard
John Deere recalls Frontier wood chippers with model numbers WC1103, WC1105, and WC1205 due to risk of injury from blades breaking and discharging during operation.
John DeereOct 17, 2017 - Use cautionVehicle
MERCEDES-BENZ SPRINTER 2500 (2016) recall — Equipment
Daimler Vans USA recalls 2016 Mercedes-Benz Sprinter 2500 vehicles with incorrect load capacity labels, risking overloading and crashes. Owners must have labels checked and replaced free by dealers.
Mercedes-BenzOct 16, 2017 - Use cautionVehicle
MERCEDES-BENZ METRIS (2017) recall — Suspension
Daimler Vans USA is recalling 2017 Mercedes-Benz Metris vans due to potential front wheel detachment. Owners must have front axle wheel bearings inspected by dealers for free.
Mercedes-BenzOct 16, 2017 - Use cautionVehicle
FORD F-550 SD (2017) recall — Latches/Locks/Linkages
Ford is recalling 2017 F-550 Super Duty trucks with door latches that may open while driving due to bent cables or water damage. Owners should contact Ford for free repairs.
FordOct 16, 2017 - Lower riskMedical device
Keystone Dental Inc recalls STAGE-1¿ RDS COC Abutment Plastic Sleeve, Non-Lock, Multi-Unit; Catalog Number: S2437-01-1K
Keystone Dental recalls non-locking abutment sleeves (catalog S2437-01-1K) due to being shipped as non-locking when they should be locking. This could cause dental lab errors during crown creation.
Keystone DentalOct 16, 2017 - Use cautionMedical device
Stryker Instruments Div. of Stryker Corporation recalls The Stryker Thoracic Pedicle Feeler 6002-350-000 is a smart instrument for remote control of the navigation software
Stryker recalls specific Thoracic Pedicle Feelers (serials 10897-10928) due to potential tip breakage from material degradation. Learn what to do if you own this instrument.
StrykerOct 16, 2017 - Lower riskMedical device
Fukuda Denshi Co., Ltd. recalls Fukuda Denshi patient monitor model DS-8100M and DS-8100N Product Usage: Use of the Fukuda Denshi DynaScope Model
Fukuda Denshi recalls DS-8100M and DS-8100N patient monitors with a rare short-term battery error due to damaged lithium-ion capacitors. Affected units may display error messages and require replacement.
Fukuda DenshiOct 16, 2017 - Lower riskMedical device
Normand Informatique recalls Remisol Advance Software (Driver Architect) Catalog Number B32129 The Remisol Advance Data Manager (Stand alone Data
Normand Informatique recalls Remisol Advance Software versions 1.6-1.9 due to potential wrong results from a software nonconformity in service settings. Affected users should contact for remedy.
Normand InformatiqueOct 16, 2017 - Lower riskMedical device
C.R. Bard, Inc. recalls Medivance ArcticGel Small Pad Kit - a box containing a single foil pouch, which contains a set of four (4) pads. A set
C.R. Bard recalls ArcticGel Small Pad Kit due to hydrogel peeling from pads. This may cause skin irritation or discomfort during use. Affected units include specific product codes and lots.
C.R. BardOct 16, 2017 - Lower riskMedical device
DeRoyal Industries Inc recalls DeRoyal Sterile Custom kits containing Medline Aplicare Povidone Iodine Prep Pads: a) Incision and Drainage Tray, REF
DeRoyal recalls sterile surgical kits containing Medline Aplicare Povidone Iodine Prep Pads with incorrect expiration dates. Affected kits include specific tray and pack models with listed lot numbers. Consumers should check their kit's reference numbers and lot numbers to determine if recalled.
DeRoyalOct 16, 2017 - Stop using nowFood
RELISH FOODS, INC. recalls Newport -Yellowfin Tuna Steaks; (4 oz. and 6 oz.) Frozen, packed in 10 lb. (160 oz.) 4.54 KG cardboard box. Product of
Relish Foods recalls Newport frozen Yellowfin Tuna Steaks due to Salmonella contamination. Check lot numbers GND 0697B, GND 0707C, and GND 0727A.
NewportOct 16, 2017 - UnratedFood
Brenckle Farms recalls Fresh Cilantro BRENCKLE FARMS INC Hartville, Ohio
Brenckle Farms recalls fresh cilantro due to Listeria monocytogenes contamination. Consumers should avoid eating the product to prevent potential illness.
Brenckle FarmsOct 16, 2017 - Lower riskFood
Midway Specialty Vehicles LLC recalls Triple Chocolate Mudslide Cookie, 120 1 oz. cookies, frozen
Aunt Beths Cookies voluntarily recalls Triple Chocolate Mudslide cookies sold between January 2017 and September 2017 due to potential peanut or tree-nut allergens.
Aunt Beths CookiesOct 16, 2017 - Lower riskMedical device
Medtronic Minimally Invasive Therapies Group recalls MAHURKAR"* Elite 12 FR x 16cm Acute Dual Lumen Dialysis Catheter with Curved Extensions, IC Trays. Product Number:
Medtronic recalls one lot of Elite 12 FR x 16cm Acute Dual Lumen Dialysis Catheters with Curved Extensions that were shipped without sterilization. This unsterilized product poses infection risk. Affected units have specific lot numbers and UDI codes.
MedtronicOct 14, 2017 - Lower riskMeat & poultry
Battistoni Italian Specialty Meats, LLC, Recalls Salami and Capocollo Products Due To Possible Foreign Matter Contamination
USDA FSIS recalls Battistoni salami and capocollo products from 2017 with possible aluminum contamination. Consumers should check labels for lot codes and sell-by dates to determine if affected.
BattistoniOct 13, 2017 - Use cautionMeat & poultry
Vermont Livestock Slaughter And Processing LLC, Recalls Ground Beef Due To Possible E. Coli O157:H7 Contamination
Recall of ground beef products from Bread & Butter Farm that may contain E. coli O157:H7. Consumers urged not to consume these products.
Bread & Butter FarmOct 13, 2017 - Use cautionVehicle
ELDORADO MOBILITY AMERIVAN (2015) recall — Fuel System, Gasoline
Eldorado Mobility is recalling 2010-2017 Amerivan vehicles with potential fuel leaks that could cause fire if near ignition sources. Owners must have fuel lines replaced free of charge.
Eldorado MobilityOct 13, 2017 - Lower riskMedical device
Ecolab, Inc. recalls Disposable Light Handle Cover, Item Number B1-715-65. Packaged 1 device inside a peel pouch and sealed. Sealed pouches
Ecolab recalls disposable light handle covers (item B1-715-65) due to potential gaps in sealed pouches that could allow contamination. Affected units include specific lot numbers from 14224 to 17192. Consumers should check their product labels and contact Ecolab for details.
EcolabOct 13, 2017 - Lower riskMedical device
Cook Inc. recalls Coons Interventional Wire Guide
Cook recalls Coons Interventional Wire Guides with heparin coating not labeled. Affected units have specific lot codes. Contact for details.
CookOct 13, 2017
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83,390 recalls tracked · 71,917 explained in plain English · 10,946 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.