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- Lower riskFood
Crown Candy Corporation recalls Old Fashioned Coconut Bon Bons; Net Wt. 6.5 OZ. (184g); Manufactured by Crown Candy Corporation; Confectionery product
Crown Candy Corporation recalls Old Fashioned Coconut Bon Bons due to mislabeled allergens. Products may contain undeclared pecans or coconut. Check UPC 041466031238 and lot numbers for affected items.
Crown Candy CorporationDec 27, 2017 - Lower riskFood
Schmidt Baking Co., Inc. recalls BUTTER MILK ( Under the following Trade Names - SUNBEAM 2PK, SUNBEAM )
Schmidt Baking Co. recalls Butter Milk (SUNBEAM 2PK, SUNBEAM) due to potential foreign material. Consumers should check Julian codes 344 or 345 for affected products.
Schmidt Baking CoDec 27, 2017 - Stop using nowConsumer product
Rocky Mountain Bicycles Recall Mountain Bicycles Due to Crash Hazard
Rocky Mountain recalls 2018 mountain bikes with unsecured brake cable housing that can cause brake failure and crashes. Consumers must stop using immediately and get free repair.
Rocky MountainDec 27, 2017 - Use cautionConsumer product
HealthPostures Recalls IntimateRider Chair and RiderMate Bench Due to Fall Hazard (Recall Alert)
HealthPostures recalls IntimateRider chairs and RiderMate benches due to loose stitching causing fall risks. Consumers must stop using and get free replacement covers.
HealthPosturesDec 27, 2017 - Stop using nowMeat & poultry
Swift Beef Company Recalls Beef Stew Products Due to Possible Foreign Matter Contamination
Swift Beef Co. recalls ~4,702 lbs of HEB beef stew meat due to possible plastic and metal contamination. Check your product details.
JBS USA / HEBDec 26, 2017 - Use cautionVehicle
NEWMAR CANYON STAR (2017) recall — Service Brakes, Hydraulic
Newmar is recalling 2017 Canyon Star vehicles with potential brake fluid leaks causing longer stopping distances. Owners must have HECU valve block ball plugs checked by Ford/Lincoln dealers.
NewmarDec 26, 2017 - Use cautionVehicle
TIFFIN BUS (2018) recall — Equipment
Tiffin recalls certain 2009-2018 bus models with potentially defective fire extinguishers that could fail during a fire, increasing injury risk. Owners must contact Kidde for a free replacement.
TiffinDec 22, 2017 - Use cautionVehicle
KENWORTH T680 (2018) recall — Power Train
PACCAR recalls 2018 Kenworth T680 trucks with faulty transmission control modules that may cause unintended vehicle movement when starting, risking crashes. Owners must update software free of charge.
KenworthDec 22, 2017 - Use cautionMedical device
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls LATARJET EXPERIENCE Sharp Curved Ostetome Product Usage: The Latarjet EXPERIENCE Instability Shoulder Set is intended
DePuy Mitek recalls Latarjet Experience Instability Shoulder Sets due to reports of loosening or unscrewing from the handle. Affected models include 16D01, 16D02, 16K01, 17A01, 17B01, 17B02.
DePuy MitekDec 22, 2017 - Lower riskMedical device
Medtronic Sofamor Danek USA Inc recalls Medtronic ANGLED DRILL, REF 6630902, QTY: 1 EA Rx only
Medtronic recalls a single angled drill (REF 6630902) due to a longer drill tip extension than specified, which may cause improper use. Affected units have UDI 00643169363502 and lot number EM17F015.
Medtr: A short, human brand name for headings (e.g.Dec 22, 2017 - Lower riskMedical device
Roche Diagnostics Corporation recalls Elecsys BRAHMS PCT Immunoassay for the in vitro quantitative determination of PCT (procalcitonin) in human serum and
Roche recalls Elecs: BRAHMS PCT Immunoassay due to decreased patient sample recovery on certain analyzers. This may affect lab results accuracy. Affected units include specific lot numbers.
RocheDec 22, 2017 - Stop using nowMedical device
Arrow International Inc recalls (1) Central Venous Catheterization Kit, Part Number (PN): ASK-04300-PHP; (2) Single-Lumen Central Venous
Arrow recalls specific catheter kits due to potential sterility issues. Affected lots may not be sealed properly, risking infection. Consumers should check lot numbers and contact Arrow for details.
ArrowDec 22, 2017 - Lower riskDrug
Hetero Labs Limited Unit V recalls Famciclovir Tablets, 500 mg, 30-count bottles, Rx Only, Manufactured For: Camber Pharmaceuticals. Inc. Piscataway, NJ
Hetero Labs recalls 500mg Famciclovir tablets due to temperature abuse causing tablets to become wet and disintegrated. Rx-only product manufactured for Camber Pharmaceuticals.
Hetero Labs LimitedDec 22, 2017 - Stop using nowDrug
Hetero Labs, Ltd. - Unit III recalls Simvastatin Tablets, USP, 40 mg, 1000-count bottle, Rx only, Manufactured for: Camber Pharmaceuticals, Inc.,
Hetero Labs recalls Simvastatin Tablets USP 40 mg (1000-count) due to a metallic razor blade found in one bottle. Check your lot number.
Hetero LabsDec 22, 2017 - Lower riskFood
Coconuthead, LLC recalls CO YO Coconut Yogurt Alternative CHOCOLATE, 5.3 oz and 12 oz. plastic container, 6 packages per case. Store between 36
Coconuthead LLC recalls CO YO Chocolate Yogurt Alternative due to container bloating. Consumers should check product labels for 5.3oz and 12oz plastic containers. No remedy specified in official notice.
CoconutheadDec 22, 2017 - Lower riskFood
Harris Teeter Distribution Ctr recalls Harris Teeter's HT Traders Mama Biscotti Mini Biscotti, Triple Chocolate, UPC: 7203670827.
Harris Teeter recalls Mama Biscotti Mini Biscotti, Triple Chocolate with undeclared almonds. Consumers should check UPC 7203670827 and lot 17338 for affected items.
Harris TeeterDec 22, 2017 - Lower riskFood
Bellisio Foods Inc recalls Michelina's Fettuccine Alfredo NET WT. 8.5 oz package Frozen CONTAINS MILK, WHEAT BELLISIO FOODS, INC., DULUTH, MN
Bellisio Foods recalls Michelina's Fettuccine Alfredo frozen packages due to undeclared soy from chicken contamination. Consumers should check product codes and contact Bellisio Foods for details.
Bellisio FoodsDec 22, 2017 - Use cautionFood
Nodine's Smokehouse Inc. recalls Smoked salmon in 1.5 oz. and 8 oz. packages
Nodine's Smokehouse recalls smoked salmon packages (1.5 oz and 8 oz) due to potential Listeria monocytogenes contamination. Consumers should check product codes 40173 and 33173 for affected items.
Nodine's SmokehouseDec 22, 2017 - Lower riskFood
Daisy's Bakery Inc. recalls Daisy s Bakery Inc., Gourmet Concha, 4 oz. / 1 per package, Plastic Bag, 12 units per case
Daisy's Bakery is recalling Gourmet Concha 4oz packages due to undeclared milk allergen. Consumers should check product codes 441-471 for affected items.
Daisy's BakeryDec 22, 2017 - Lower riskFood
AJC International, Inc. recalls Early Dawn; Whole Tilapia IQF, Gutted & Scaled, Farm Raised, 40 lbs.; Size 550-750g OR 750g+, Lot No.: 1985507;
AJC International recalls Early Dawn Whole Tilapia IQF, Gutted & Scaled, Farm Raised, 40 lbs. (Size 550-750g or 750g+) due to sulfadiazine antibiotic contamination. Consumers should check lot numbers and contact the company for details.
AJC InternationalDec 22, 2017 - Stop using nowConsumer product
Vilo Home Recalls Marseille Dining Benches Due to Fall Hazard
Vilo Home recalls Marseille dining benches with a risk of collapse due to foam cushion cracking, causing falls. Consumers must stop using and get a refund.
Vilo HomeDec 22, 2017 - Stop using nowConsumer product
ACE Work Boots Recalled by Shoes for Crews Due to Injury Hazard (Recall Alert)
Shoes for Crews recalls ACE work boots (styles #76054 and #77667) due to missing puncture-resistant plate, risking injuries. Consumers should stop using and get refunds.
Shoes for CrewsDec 22, 2017 - Use cautionMeat & poultry
PFP Enterprises LLC Recalls Ground Beef Products Due to Misbranding and an Undeclared Allergen
USDA recalls 7,570 lbs of ground beef products from PFP Enterprises due to soy allergen not declared on labels. Consumers and institutions urged to stop using these products.
PFP EnterprisesDec 21, 2017 - Use cautionVehicle
MASERATI GHIBLI (2018) recall — Fuel System, Gasoline
Maserati is recalling 2018 Ghibli models with a potential fuel leak in the engine that could cause fire. Owners must contact dealers for free repair by February 9, 2018.
MaseratiDec 21, 2017 - Use cautionVehicle
FOREST RIVER CHEROKEE (2018) recall — Electrical System
Forest River recalls 2015-2018 Cherokee trailers due to wiring that may pinch, causing short circuits and fire risk. Owners should contact customer service for free wire rerouting.
Forest RiverDec 21, 2017 - Use cautionVehicle
CHRYSLER PACIFICA (2018) recall — Equipment
Chrysler is recalling 2018 Pacifica vehicles with certain Kidde fire extinguishers that may become clogged or detach, increasing fire injury risk. Owners must contact Chrysler or Kidde for a free replacement.
ChryslerDec 21, 2017 - Lower riskMedical device
Arrow International Inc recalls ARROWg+ard Blue PLUS catheter, Catalog Number: ASK-45854-NG Product Usage: The ARROWg+ard Blue PLUS¿ catheter permits
Arrow recalls ARROWg+ard Blue PLUS catheters with missing lot numbers and expiration dates. These catheters may not be safe for use due to incomplete labeling.
ArrowDec 21, 2017 - Lower riskMedical device
Howmedica Osteonics Corp. recalls Custom Made Implant System with Minimum Invasive Grower (MIG) component
Howmedica recalls custom implant systems made between March 2007 and October 2014 due to outdated instructions that don't clarify locking mechanism function and warnings for the locking screw. Affected users should contact the company for details.
HowmedicaDec 21, 2017 - Lower riskMedical device
Quantimetrix Corporation recalls Dropper Plus Point-of-Care Urinalysis Dipstick Control kit The Quantimetrix Dropper Plus Point-of-Care Urinalysis
Quantimetrix recalls Dropper Plus Point-of-Care Urinalysis Dipstick Control kits with incorrect lot numbers. Affected kits contain faulty vials that may not work properly for urinalysis tests.
QuantimetrixDec 21, 2017 - Lower riskMedical device
Stryker Corporation recalls 3910-090-800 ASSY, PKG, 8.0MM X 90MM DRI-LOK THREADED CANNULA, 5 units per box. The Disposable Cannula device is
Stryker recalls 5-unit boxes of disposable cannulas with expired expiration dates (August 2018 marked but should be 2016). Affected units may pose safety risks if used after expiration.
StrykerDec 21, 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.