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
34,943 found- Lower riskFood
Teasource recalls TeaSource Roasted Chestnut, loose leaf tea. packaged in 16 oz. (454g)Metal/Poly non-resealable bag, and 4 oz., and 2
Teasource recalls loose leaf Roasted Chestnut tea due to undeclared slivered almonds. Consumers should check product packaging for 16oz, 4oz, or 2oz bags sold in the US.
TeasourceJul 27, 2018 - Lower riskFood
Mojave Foods Corp. recalls El Guapo Jamaica Hibiscus Flowers in flexible pouches , 1 oz., 2 oz., 8 oz., 16 oz., and 10 lb. box .
Mojave Foods Corp. recalls El Guapo Jamaica Hibiscus Flowers pouches due to undeclared allergen. Check UPCs and best-by dates for affected products.
Mojave Foods Corp.Jul 27, 2018 - Stop using nowFood
Lipari Foods, Inc. recalls Premo Brand and Fresh Grab turkey and Swiss submarine sandwiches, 4/6 oz, and 18/6 oz.
Lipari Foods recalls specific lots of Premo and Fresh Grab turkey and Swiss submarine sandwiches due to potential Listeria monocytogenes contamination.
Premo / Fresh GrabJul 27, 2018 - Stop using nowFood
Fresh Express Incorpated recalls McDonalds Salad Ingredients, 9.25 lb, Salad Blend Romaine, Carrot & Spinach, Kale, Red Leaf Lettuce
Fresh Express recalls specific lots of McDonald's Salad Ingredients due to a positive test for the Cyclospora organism. Check your product codes and use-thru dates.
Fresh ExpressJul 27, 2018 - UnratedFood
Seroyal International, a division of Atrium Innovations recalls Genestra brand AFA-gen capsule 15 mg Niacin/ capsule 300 mg Blue Green Algae / capsule 2 capsules, twice daily Dietary
Seroyal International recalls Genestra AFA-gen capsules due to microcystins exceeding safety limits. Consumers should check product details and contact for guidance.
Seroyal InternationalJul 27, 2018 - Stop using nowConsumer product
Hirsch Gift Recalls Wireless Charging Pads Due to Burn Hazard
Hirsch Gift recalls CloudCharge Qi Wireless Charging Pads due to burn hazard from overheating. Consumers should stop using and get a free replacement.
Hirsch GiftJul 27, 2018 - Use cautionVehicle
JEEP CHEROKEE (2018) recall — Power Train
Chrysler recalls certain 2018 Jeep Cherokee vehicles due to potential halfshaft bearing cage failure causing loss of drive or unintended movement in Park. Owners must contact Chrysler for free replacement.
ChryslerJul 26, 2018 - Use cautionVehicle
CHRYSLER PACIFICA (2018) recall — Power Train
Chrysler recalls 2018 Pacifica vehicles with potentially unsafe axle shafts that could cause loss of drive or unintended movement in Park, increasing crash risk. Owners must contact Chrysler for free replacement.
ChryslerJul 26, 2018 - Use cautionVehicle
JEEP CHEROKEE (2019) recall — Power Train
Chrysler recalls certain 2019 Jeep Cherokee vehicles due to potential transmission failure causing loss of motion, increasing crash risk. Owners must contact for free transmission replacement.
ChryslerJul 26, 2018 - Lower riskMedical device
Steris Corporation recalls AMSCO V-PRO 1, V-PRO 1 Plus, and V-PRO maX Low Temperature Sterilization Systems The V-PRO 1, V-PRO 1 Plus, and V-PRO
Steris Corporation is a global leader in medical device manufacturing and healthcare solutions. We provide innovative products and services to improve patient care and operational efficiency in healthcare settings.
SterisJul 26, 2018 - Lower riskMedical device
Covidien LLC recalls Li-ion battery packs used in BIS Vista and BIS View Monitoring Systems. Product Number/CFN: 186-0208 UDI-Device
Covidien recalls Li-ion battery packs for BIS Vista and BIS View Monitoring Systems with date code 3114 or older (week 31, 2014) due to revised replacement instructions.
CovidienJul 26, 2018 - Lower riskMedical device
Stryker GmbH recalls Hoffmann LRF Hexapod Software Catalog #: 983031 Software Version #: HLRF 1.0-2/002, HLRF 1.1-2/002
Stryker recalls specific Hexapod software versions due to potential erroneous axial correction plans when creating correction plans with certain settings. Affected users should contact Stryker for details.
StrykerJul 26, 2018 - Lower riskMedical device
Cambridge Sensors Limited recalls Microdot Xtra blood glucose test strips
Cambridge Sensors recalls specific Microdot Xtra blood glucose test strips due to improper fit causing delayed test results. Affected lots listed in the notice.
Cambridge SensorsJul 26, 2018 - UnratedDrug
H J Harkins Company Inc dba Pharma Pac recalls Valsartan tablets 160 mg, 90-count bottle, Rx Only, Repackaged by H.J. Harkins Co, Inc. Grover Beach, CA 93433, NDC
Pharma Pac recalls 160mg Valsartan tablets due to detected carcinogen impurity in manufacturing. Affected products have specific labeling and lot numbers. Consumers should contact the company for details.
Pharma PacJul 26, 2018 - Lower riskDrug
Lupin Pharmaceuticals Inc. recalls Moxifloxacin Ophthalmic Solution USP, 0.5%, 5 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals Inc.
Lupin Pharmaceuticals recalls 0.5% moxifloxacin eye drops due to impurities detected in stability testing. Affected lots may cause eye injury if used. Contact for return instructions.
Lupin PharmaceuticalsJul 26, 2018 - Lower riskDrug
Right Value Drug Stores, Inc. recalls Testosterone 200 mg Pellet, Rx only, Carie Boyd's Prescription Shop 122 Grapevine Hwy., Hurst, TX 76054, 800-930-4361
Right Value Drug Stores recalls testosterone pellets with incorrect expiration dates on labels. Consumers should check labels for lot #061918@08 and expiration 11/28/2019.
Right Value Drug StoresJul 26, 2018 - Lower riskFood
Confidence Inc./Confidence U.S.A. Inc. recalls FP0392, Confidence, Glucosamine Plus, with White Willow Bark & Boswella, 90 Extended Release Tablets, UPC# 8 10891
Confidence recalls Glucosamine Plus tablets with undeclared ingredients like HPMC, Titanium Dioxide, and PEG. Consumers should check product details to determine if affected.
ConfidenceJul 26, 2018 - Use cautionFood
KRAFT HEINZ FOODS COMPANY recalls Food Network Kitchen Inspirations Asian Style Sesame Ginger Dressing. 12 oz glass bottle, 6 bottles per case Shelf
Kraft Heinz recalls Food Network Kitchen Inspirations Asian Style Sesame Ginger Dressing due to premature spoilage from bacteria. Check your bottle dates.
Food Network Kitchen InspirationsJul 26, 2018 - Use cautionConsumer product
Trek Recalls Bontrager Line Pro Bicycle Pedals Due to Fall Hazard
Trek recalls Bontrager Line Pro flat bicycle pedals due to spindle breakage causing fall hazards. Consumers should stop using and get free repairs from Trek retailers.
TrekJul 26, 2018 - Stop using nowConsumer product
Jimmy Hack Golf Recalls Golf Swing Trainers Due to Injury Hazard
Jimmy Hack Golf recalls Orange Whip swing trainers (models OWT/OWM) with batch numbers 772-792 due to orange ball detaching during use, posing injury risk to users and bystanders.
Jimmy Hack GolfJul 26, 2018 - Lower riskMedical device
The Binding Site Group, Ltd. recalls Binding Site Human IgM Kit (for SPAPLUS), REF: NK012.S The device consists of reaction buffer, sheep anti-IgM
Binding Site recalls Human IgM Kit (SPAPLUS) REF NK012.S due to reduced accuracy after calibration. Affected lots 407483-1 and 407483-2 may produce inaccurate results.
The Binding SiteJul 25, 2018 - Use cautionMedical device
Hycor Biomedical LLC recalls HYTEC Stop Solution (Allergy), 300ml bottle containing 1N sodium hydroxide solution, Part # 308051, sold separately or
Hycor Biomedical recalls 300ml HYTEC Stop Solution bottles with 1N sodium hydroxide that have leaked. These caustic solutions can cause skin burns. Affected units include specific lot numbers and kits.
Hycor BiomedicalJul 25, 2018 - Use cautionMedical device
Med-Mizer, Inc. recalls PR1000 Pivot Rehab Bed AC powered adjustable bed.
Med-Mizer recalls AC-powered PR1000 Pivot Rehab Beds (2010-2014) due to wire pinching when pivoting left, requiring bed transfer until fixed.
Med-MizerJul 25, 2018 - Lower riskMedical device
Alcon Research LLC recalls Alcon Constellation Vision System 20 GA TOTALPLUS Combined Procedure Pak, Product #8065751079, Sterile. The firm name
Alcon recalls 20 GA Totalplus Procedure Pak (Product #8065751079) due to possible inclusion of 25-gauge cannula instead of 20-gauge, which could cause incorrect surgical procedures.
AlconJul 25, 2018 - Use cautionDrug
The Hain Celestial Group, Inc. - Worldwide HQ recalls alba BOTANICA Sensitive Sheer Shield Sunscreen Fragrance Free spf 50+ , 85 g 3 oz tube. Manufactured by: The Haine
The Hain Celestial Group recalls specific lots of alba BOTANICA sunscreen due to microbial contamination. Check your tube's lot code and UPC.
alba BOTANICAJul 25, 2018 - Use cautionDrug
Mylan Pharmaceuticals Inc. recalls Dymista (azelastine hydrochloride and fluticasone propionate) Nasal Spray, 137 mcg / 50 mcg per spray, packaged in a 23
Mylan recalls Dymista nasal spray due to potential glass fragments in bottles. This could cause injury if the glass breaks during use. Affected units were manufactured in India with specific lot numbers and expiration dates.
MylanJul 25, 2018 - UnratedDrug
Ranier's Compounding Laboratory recalls Triple P (Prostaglandin/Papaverine/Phentolamine) Injection, 0.008/22.5/0.83 mg/mL, packaged in a) 5 mL and b) 10 mL
Ranier's Compounding Laboratory recalls Triple P (Prostaglandin/Papaverine/Phentolamine) injections due to potential lack of sterility. This affects specific vial sizes and lot numbers. Consumers should contact the lab for details.
Ranier'sJul 25, 2018 - Lower riskFood
Bantam Bagels recalls BANTAM BAGELS The Classic Mini Stuffed Bagels PLAIN BAGEL STUFFED WITH PLAIN WHIPPED CREAM CHEESE with large white
Bantam Bagels recalls Classic Mini Stuffed Bagels with undeclared egg. Consumers should check packaging for EGG TEST 5/04/2018 or 5/4/2018 dates.
Bantam BagelsJul 25, 2018 - Lower riskFood
Severino Pasta Manufacturing, Inc. recalls Severino Home Made, Artisanal Small Batch Pasta, Raviolini Cheese, 9 units x 9 oz per case. Expiration March 2019.
Severino recalls pasta products with incorrect egg labeling. Consumers may be confused about ingredient presence due to mismatched labels on the same product.
SeverinoJul 25, 2018 - Lower riskMedical device
Mako Surgical Corporation recalls Stryker Mako Vizadisc Knee Procedure Tracking Kit
Stryker Mako recalls specific lots of Vizadisc Knee Procedure Tracking Kit due to reflective material damage causing camera detection issues. Affected units include catalog numbers 107120 with listed lot numbers.
Stryker MakoJul 24, 2018
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