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 riskMedical device
Dynavox Systems Llc recalls Dynavox T10 Speech Generating Device ( including Batteries)
Dynavox recalls T10 speech devices with batteries that may swell or separate after months of inactivity. Owners should check serial numbers for affected units.
DynavoxDec 14, 2017 - Lower riskMedical device
Kalila Medical recalls Vado Steerable Sheath 8.8F, REF SS8FMU67, packaged in a lidded tray that is within a pouch which is inserted into a
Kalila Medical recalls Vado Steerable Sheath 8.8F (REF SS8FMU67) due to potential torn liner material from manufacturing defects. Affected units were shipped with specific lot numbers and expiration dates.
Kalila MedicalDec 14, 2017 - UnratedDrug
Teva Pharmaceuticals USA recalls Moexipril Hydrochloride and Hydrocholorothiazide Tablets USP, 7.5 mg/12.5 mg, 100-count bottle, Rx only, Distributed
Teva recalls 7.5mg/12.5mg Moexipril-Hydrochlorothiazide tablets due to high impurity levels detected in stability testing. This may pose a risk to patients using prescription medication.
Teva PharmaceuticalsDec 14, 2017 - Lower riskDrug
Boehringer Ingelheim Pharmaceuticals, Inc. recalls SPIRIVA HandiHaler (tiotropium bromide inhalation powder) 18 mcg/capsule (90 capsules (unit dose blisters) per box, Rx
Boehringer Ingelheim recalls SPIRIVA HandiHaler inhalers with failed stability specifications. This may affect safety and effectiveness of the medication.
Boehringer IngelheimDec 14, 2017 - UnratedDrug
SHISEIDO AMERICA INC. recalls Shiseido Future Solution LX Universal Defense SPF 50+ (octinoxate 4.9%, octocrylebe 3.0%, oxybenzone 1.0% and zinc
Shiseido recalls Future Solution LX Universal Defense SPF 50+ due to manufacturing quality deviations. This may affect product safety. Check NDC 58411-256-60 or SKU numbers for affected items.
ShiseidoDec 14, 2017 - Stop using nowFood
American Sugar Refining, Inc. recalls Sugar Syrup / Bulk / Tanker Truck #1 & 2
American Sugar Refining recalls bulk sugar syrup from tanker trucks due to metal contamination. Check lot numbers and distribution states.
American Sugar RefiningDec 14, 2017 - UnratedFood
Nyblad Orchards recalls Golden delicious whole fresh apples, Apple Ridge 5lb, 2-3/4 apples, packaged in red net mesh bags " 3lb, 2-1/2 apples,
Nyblad Orchards is recalling multiple apple varieties sold in various pack sizes due to potential Listeria monocytogenes contamination. Consumers should check product labels for specific lot numbers.
Nyblad OrchardsDec 14, 2017 - Use cautionConsumer product
Todd Snyder Recalls Sweatshirts Due to Violation of Federal Flammability Standards
Todd Snyder recalls men's cotton sweatshirts that fail federal flammability standards, posing burn risks. Consumers must stop using and return for refund plus $50 gift card.
Todd SnyderDec 14, 2017 - Use cautionConsumer product
Pier 1 Imports Recalls Decorative Glass Pumpkins Due to Laceration Hazard
Pier 1 Imports recalls decorative glass pumpkins with wooden stems that can detach, causing the pumpkin to fall and break, posing a laceration hazard. Consumers should stop using and return for refund or credit.
Pier 1 ImportsDec 14, 2017 - Use cautionConsumer product
Hunter Fan Recalls Ceiling Fans Due to Impact Injury Hazard; New Instructions Provided
Hunter recalls Contempo ceiling fans (models 59174, 59176) due to risk of light globe falling and causing impact injuries. Check installation by turning globe clockwise until firm. Contact Hunter or Costco for new instructions.
HunterDec 14, 2017 - Use cautionConsumer product
Crate and Barrel Recalls Benches Due to Fall Hazard (Recall Alert)
Crate and Barrel recalls Dakota wooden benches that can tip over, causing falls. Consumers must stop using and contact for free repair.
Crate and BarrelDec 14, 2017 - Use cautionVehicle
HONDA VT1300CX (2010) recall — Fuel System, Gasoline
Honda is recalling certain 2010 and 2016 VT1300CX Fury motorcycles with potential fuel tank weld defects that could cause leaks and fire if ignited.
HondaDec 13, 2017 - Use cautionVehicle
HYUNDAI SANTA FE SPORT (2018) recall — Air Bags
Hyundai recalls 2018 Santa Fe Sport vehicles with side curtain air bags that may detach during deployment, risking injury in crashes. Owners must have air bags replaced free by February 9, 2018.
HyundaiDec 13, 2017 - Use cautionVehicle
FOREST RIVER BERKSHIRE (2018) recall — Electrical System
Forest River recalls 2016-2018 Berkshire XLT motorhomes with faulty circuit breakers that may cause overheating and fire. Owners must have the circuit breaker replaced free by dealers.
Forest RiverDec 13, 2017 - Lower riskMedical device
Halyard Health, Inc recalls CORTRAK* 2 Nasogastric/Nasointestinal (NG/NI) Feeding Tubes with Electromagnetic Transmitting Stylet and CORFLO*
Halyard Health recalls CORTRAK 2 NG/NI feeding tubes with electromagnetic stylet where the stylet may be visible in the exit port window, which could cause blockage. Affected units have product code 20-9551TRAK2A.
Halyard HealthDec 13, 2017 - Use cautionMedical device
Ii - Vi Incorporated recalls 11-VI Incorporated Laser diode component Non-certified laser diode component used in laser sights for firearms
Ii-Vi Incorporated recalls non-certified laser diode components used in firearm laser sights due to exceeding 5 mW light emission limits. Affected models 25-0655 and 25-0657 sold in the U.S. since 2020.
Ii-Vi IncorporatedDec 13, 2017 - Lower riskMedical device
Smith & Nephew, Inc. recalls Smith & Nephew Taylor Spatial Frame Website software, Catalog Number 71070401. A web-based and mobile application
Smith & Nephew recalls software version 5.2.5/5.2.6 for rare inverted frame previews during surgical planning, potentially causing misalignment in bone fixation procedures.
Smith & NephewDec 13, 2017 - Lower riskMedical device
C.R. Bard, Inc. recalls Bardex Lubricath 3-Way 75cc Continuous Irrigation Foley Catheter (Creevy), 22Fr. Rx (01267522)
C.R. Bard recalls specific models of Foley catheters due to incorrect retainer cap printing, which may lead to improper use. Affected units include model 01267522 with lot numbers NGBR0383 and NGB:2129.
C.R. BardDec 13, 2017 - Lower riskMedical device
Covidien LLC recalls Signia" Power Handle (SIGPHANDLE, SIGNVAL1 and SIGVAL20 - Kits) The Signia" Power Handle, when used with Endo GIA"
C17AAG
C17AAGDec 13, 2017 - Lower riskDrug
ALLERGAN recalls INFeD (Iron Dextran Injection USP) 100 mg elemental iron/2 ml (50 mg/mL), Rx Only, packaged in a) single dose vials,
Allergan recalls INFeD (Iron Dextran Injection USP) 100 mg elemental iron/2 ml vials due to failed stability testing for iron content. This affects certain lots manufactured by Patheon Italia S.p.A. in Italy.
AllerganDec 13, 2017 - Lower riskFood
Harrisburg Dairies, Inc recalls 365 brand Egg Nog, Grade A; 1 qt. and 1/2 GAL; and Harrisburg Dairies brand Egg Nog, Grade A; 1/2 GAL, 1 Quart, 16 FL.
Harrisburg Dairies recalls 365 and Harrisburg brand Egg Nog products due to dried egg yolks not being listed in ingredient statements. Consumers should check product dates and contact the company for details.
Harrisburg DairiesDec 13, 2017 - Use cautionMeat & poultry
Santa Fe Importers, Inc. Recalls Ready-To-Eat Pork Products due to Possible Extraneous Material Contamination
USDA FSIS recalls 143 pounds of pork salami products from Santa Fe Importers, Inc. that may contain metal shavings. Consumers are urged not to consume these products and should discard or return them.
Santa Fe ImportersDec 12, 2017 - Use cautionVehicle
NEWMAR BAY STAR (2018) recall — Exterior Lighting
Newmar is recalling 2018 Bay Star motorhomes with front side marker lights not connected to wiring harness, causing low beams to fail when high beams are activated. This reduces visibility and increases crash risk. Owners should contact Newmar for free repairs.
NewmarDec 12, 2017 - Lower riskMedical device
Zimmer Biomet, Inc. recalls PERSONA¿ THE PERSONALIZED KNEE SYSTEM "PSN TIB STM 5 DEG SZ D R" indicated for patients with severe knee pain and
Zimmer Biomet recalls a specific lot of PERSONA knee implants due to missing set screw and taper plug in the packaging. This could affect proper installation and safety for patients with severe knee pain.
Zimmer BiometDec 12, 2017 - Lower riskMedical device
Encore Medical, Lp recalls EMPOWR Porous Knee System TIBIAL PUNCH, SMALL, REF 801-05-202, NON STERILE, Qty 1 For use in orthopedic surgery.
Encore Medical recalls EMPOWR Porous Knee System TIBIAL PUNCH, SMALL model for potential implant placement error during orthopedic surgery. Affected units may cause improper positioning of knee implants.
Encore MedicalDec 12, 2017 - Use cautionMedical device
Boston Scientific Corporation recalls Percutaneous Access Set, Product Number: M0064201150, GTIN: 08714729009757 The Malecot Nephrostomy Catheter Set is
Boston Scientific recalls Malecot Nephrostomy Catheters that may break at mid-shaft during use. Affected units have specific product numbers and batch dates. Stop using if you own these catheters.
Boston ScientificDec 12, 2017 - Lower riskDrug
Woodfield Pharmaceutical, LLC recalls Codeine-Guaifenesin Oral Solution 10-100 mg/5 mL Antitussive Expectorant ,16 fl. oz. , Manufactured For: Method
Woodfield Pharmaceutical recalls 16 fl oz codeine-guaifenesin oral solution due to potential Burkholderia cepacia contamination. Consumers should check product details and contact the company for guidance.
Woodfield PharmaceuticalDec 12, 2017 - Lower riskDrug
Keryx Biopharmaceuticals, Inc. recalls Auryxia (ferric citrate) tablets, 210 mg , 200-count bottles, RX ONLY, Manufactured for and distributed by: Keryx
Keryx recalls 210mg Auryxia tablets (200-count) due to silica gel desiccant potentially contacting tablets. RX-only medication for iron deficiency.
KeryxDec 12, 2017 - Stop using nowFood
Spice Chain Corporation recalls Paprika PAPA 12/5oz, International Bazaar
Spice Chain recalls Paprika PAPA 12/5oz due to beetle contamination. Check your lot numbers and see what to do if you have this product.
Spice Chain CorporationDec 12, 2017 - Stop using nowFood
Rachael's Food Corporation recalls Rachael's SPRINGFIELD SMOKED FISH LOX CREAM CHEESE SPREAD, 8 oz. and 5 lb. UPC: 045049117760
Rachael's Food Corp recalls Springfield Smoked Fish Lox Cream Cheese Spread due to possible Listeria monocytogenes contamination.
Rachael'sDec 12, 2017
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