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
SUZUKI SX4 (2013) recall — Steering
Suzuki is recalling 2012-2013 SX4 vehicles with a power steering pump that may seize, causing loss of steering assist and increased crash risk. Owners can get a free replacement pump.
SuzukiNov 14, 2018 - Use cautionVehicle
VOLKSWAGEN E-GOLF (2018) recall — Seats
Volkswagen recalls 2018 E-Golf and related vehicles for rear seat frame welding issues that could increase injury risk in crashes. Owners must have seats inspected by dealers for free.
VolkswagenNov 14, 2018 - Stop using nowVehicle
FORD EXPLORER (2018) recall — Fuel System, Gasoline
Ford recalls certain 2018 Explorers due to a fuel leak from the pressure sensor. Dealers will replace the assembly free of charge.
FordNov 14, 2018 - Use cautionVehicle
FORD EXPEDITION (2018) recall — Seats
Ford is recalling 2018 Expedition vehicles with second row center seats that may lack J-channel reinforcement brackets, increasing crash injury risk. Owners should contact Ford for free seat inspections and repairs.
FordNov 14, 2018 - Use cautionVehicle
LINCOLN NAUTILUS (2019) recall — Air Bags
Ford is recalling 2019 Lincoln Nautilus vehicles without Adaptive Front Steering due to potential air bag cover detachment during deployment, which could increase injury risk in crashes. Owners should contact Ford for free replacement of the driver air bag module.
FordNov 14, 2018 - Use cautionVehicle
FORD F-250 SD (2019) recall — Power Train
Ford recalls 2019 F-250 Super Duty vehicles with potential unintended movement causing crash risk. Owners must have transmission inspected and replaced if needed.
FordNov 14, 2018 - Use cautionVehicle
BLUE BIRD ALL AMERICAN (2019) recall — Equipment
Blue Bird recalls 2007-2019 All American ambulances due to stretchers clamps failing under load, risking patient injury. Owners must contact Blue Bird for free clamp replacement.
Blue BirdNov 14, 2018 - Lower riskMedical device
Arrow International Inc recalls Arrow CVC 2 Lumen, Pediatric Two-Lumen Central Venous Cauterization Set with Blue FlexTip Catheter, 4 Fr 2 Lumen 5cm,
Arrow recalls pediatric central venous catheter sets with incorrect priming volume and flow rates. Affected units sold in specific lots; contact Arrow for details.
ArrowNov 14, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Lineum 4.35mm x 28mm Translation Screw, Model No. 14-524728 The Lineum OCT Spine System is intended to provide
Zimmer Biomet recalls Lineum 4.35mm x 28mm Translation Screw (Model 14-524728) due to incorrect 24mm marking on tulip head. This could lead to improper spinal alignment during surgery. Affected patients should contact manufacturer for details.
Zimmer BiometNov 14, 2018 - Use cautionMedical device
In2bones USA, LLC recalls NeoSpan SuperElastic Compression Staple w/Instruments, Size 10x10x10, Part Number T50 SN010
In2bones recalls NeoSpan SuperElastic Compression Staple kits with wrong 3mm drill bit (should be 2mm). Affected lots: 9G88C0. Stop using immediately to avoid injury.
In2bonesNov 14, 2018 - Lower riskMedical device
Diagnostica Stago, Inc. recalls Staclot LA 20 (REF 00594) The Staclot¿ LA and Staclot¿ LA 20 test kits are reagent systems designed for the qualitative
Diagnostica Stago recalls Staclot LA 20 test kits with reported shortened results. Affected lots may cause inaccurate lupus anticoagulant testing.
Diagnostica StagoNov 14, 2018 - Use cautionMedical device
Swissray Medical AG recalls ddRCombi Plus FP, Model Number 8.2000.0070.0 (US Version), 8.2000.0060.0 (Europe Version) The ddRCombi Plus FP is a
Swissray Medical recalls specific X-ray models due to rare risk of arm dropping during patient positioning, potentially causing serious injury. Affected units have serial numbers S403088, S403089, S403165.
Swissray MedicalNov 14, 2018 - Use cautionDrug
Ascend Laboratories LLC recalls Quetiapine Tablets USP 400 mg, 100 tablet bottles, Rx Only, Manufactured by: Alkem Laboratories Ltd., Mumbai - 400 013,
Ascend Laboratories recalls 400mg Quetiapine tablets with metal shard risk. Stop using if you have these specific bottles. Details include NDC 67877-248-01 and lot 7143908.
Ascend LaboratoriesNov 14, 2018 - Stop using nowFood
Harb Dairy, Inc. DBA Green Cedar Dairy recalls Green Cedar Ackawi cheese in small clear plastic shrink wrapped packaging bearing a sell by date of March 26, 2019 or
Green Cedar Dairy recalls Ackawi cheese with March 26, 2019 sell-by date due to Listeria monocytogenes contamination. Consumers should check packaging for the date and refrigerate properly.
Green Cedar DairyNov 14, 2018 - Use cautionVehicle
VOLVO V60 (2018) recall — Electrical System
Volvo is recalling certain 2018 V60 vehicles due to GPS not sending location data to emergency services during crashes. Owners must contact Volvo for free software update.
VolvoNov 13, 2018 - Lower riskMedical device
Stryker Neurovascular recalls Stryker Neurovascular, Merci 9F, 80cm, Balloon Guide Catheter, REF 90077, CE 0459, UPN Product No. 90077, UDI #:
Stryker Neurovascular recalls 9F Balloon Guide Catheters due to labeling error where 8F catheters were packaged with 9F. This affects specific lot numbers sold outside the US. No action needed as the product was not distributed in the US.
Stryker NeurovascularNov 13, 2018 - Lower riskMedical device
RVO 2.0, INC recalls Raindrop Near Vision Inlay, REF: RD1-1, Sterile, Rx Only, Manufacturer ReVision Optics, Inc.
ReVision Optics recalls Raindrop Near Vision Inlays (RD1-1) due to increased corneal haze risk after implantation. All unused products are affected. Contact for remedy details.
ReVision OpticsNov 13, 2018 - Use cautionMedical device
Stryker Communications recalls EDS Light Suspension, Central Axis, a component of the Stryker Visum LED Surgical Lighting System, with the following
Stryker recalls EDS Light Suspension components for potential insufficient joint assembly, risking surgical lighting system failure during procedures. Affected units include specific catalog numbers and serial ranges.
StrykerNov 13, 2018 - Lower riskMedical device
bioMerieux, Inc. recalls VITEK¿ 2 Systems Software Version 9.01 Update Kit.
bioMerieux recalls VITEK 2 Systems Software Version 9.01 Update Kit due to potential incorrect organism identification and antimicrobial susceptibility testing results when using the FLEXPREP feature.
bioMerieuxNov 13, 2018 - Lower riskFood
Thatchers Gourmet Specialties Inc. recalls Gingerbread Popcorn. 8 ounce (227 grams) flexible plastic bag. Brand name of Disney Theme Park Merchandise or Disney
Thatchers Gourmet recalls gingerbread popcorn for not listing wheat in ingredients. This affects Disney Theme Park merchandise sold at Disney Parks. Consumers should check UPC codes and lot numbers for affected items.
ThatchersNov 13, 2018 - Lower riskFood
Nor Cal Food Solutions LLC recalls Purveyors Kitchen Pumpkin Pesto Tapenade; NET WT 7.75 oz. (220G) UPC: 0 37677 01624 9 Ingredients: Water, Pumpkin,
Purveyors Kitchen recalls pumpkin pesto tapenade due to missing walnut allergen declaration. Check UPC 037677016249 for affected products. No remedy provided in recall notice.
Purveyors KitchenNov 13, 2018 - Lower riskFood
Smartypants Vitamins recalls Smartypants Kids Complete, Non GMO Multi and omega 3's vitamin D3 for bones, vitamin B12 for Energy: 90 gummies. UPC 8
Smartypants recalls 90-count gummy vitamins due to foreign objects found in bottles. Consumers should check UPC 85136004255 for affected products.
SmartypantsNov 13, 2018 - Lower riskFood
Tom Sturgis Pretzels, Inc. recalls Little Ones Pretzels¿ 4.5lb, 1 polyethylene bag per corrugated container .
Tom Sturgis Pretzels recalls Little Ones Pretzels (4.5lb bags) due to mislabeling that may contain milk allergen in products labeled as milk-free. Consumers should check for the UPC 70104 30055.
Tom Sturgis PretzelsNov 13, 2018 - Stop using nowFood
Quaker Manufacturing, LLC recalls Cap'n Crunch's Peanut Butter Crunch Cereal packaged in 17.1 ounce and 16.5 ounce cardboard boxes. Distributed by The
Quaker recalls Peanut Butter Crunch Cereal with Salmonella contamination. Stop using if you have 17.1oz or 16.5oz cardboard boxes from lots 110218L or 110318L.
QuakerNov 13, 2018 - Stop using nowConsumer product
YTL International Recalls Log Splitters Due to Injury Hazard (Recall Alert)
YTL International recalls 2018 County Line 40-ton hydraulic log splitters with specific serial numbers due to risk of tank disconnect causing injury. Affected units have black/grey color and Country Line printed on cylinder. Contact YTL for free replacement tongue box.
County LineNov 13, 2018 - Use cautionVehicle
PRIME TIME TRACER (2019) recall — Power Train
Forest River recalls 2019 Primetime Tracer trailers with potentially overheating hub bearings that could cause handling issues and crashes. Owners must have hubs inspected and repaired free by dealers.
Forest RiverNov 12, 2018 - Use cautionVehicle
BLUE BIRD ALL AMERICAN (2019) recall — Parking Brake
Blue Bird is recalling 2019 All American transit buses due to parking brake cable disengagement that could cause unintended bus movement. Owners must contact Blue Bird for free repair to comply with safety standards.
Blue BirdNov 12, 2018 - Use cautionVehicle
BLUE BIRD ALL AMERICAN (2019) recall — Parking Brake
Blue Bird is recalling certain 2019 All American school buses due to parking brake cable disengagement risk. Owners must contact Blue Bird customer service for free repair to prevent unintended bus movement.
Blue BirdNov 12, 2018 - Lower riskMedical device
Bracco Injeneering S.A. recalls Empower FastLoad CT Syringe Pack -sterile disposable syringe kit for use with the EmpowerCT¿, EmpowerCTA¿ and
Bracco recalls Empower FastLoad CT Syringe Packs due to insufficient sterile barrier seals, risking contamination. Affected units sold with EmpowerCT, EmpowerCTA, and EmpowerCTA+ systems. Contact for remedy.
BraccoNov 12, 2018 - Lower riskMedical device
RAYSEARCH LABORATORIES AB recalls RayStation 3.5, RayStation 4.0, RayStation 4.5, RayStation 4.7, RayStation 5, RayStation 6, RayStation 7 and RayStation
RaySearch Laboratories recalls specific RayStation software versions due to incorrect isocenter shifts in dose tracking calculations, which could affect radiation therapy accuracy.
RaySearch LaboratoriesNov 12, 2018
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