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- Use cautionVehicle
DODGE DURANGO (2014) recall — Service Brakes
Chrysler recalls certain 2011-2014 Dodge Durango vehicles with improperly installed brake booster shields that may reduce braking ability, increasing crash risk. Owners should contact dealers for free inspection.
ChryslerSep 18, 2017 - Use cautionMedical device
MicroPort Orthopedics Inc. recalls MicroPort Orthopedics SCHANZ SCREW SELF DRILL, SIZE 4mm, REF 20070057, STERILE R Product Usage: MPO Total Hip Systems
MicroPort Orthopedics recalls SCHANZ SCREWS with defective sterile pouch seals that could cause infections during hip surgery. Affected units include specific model and lot numbers for total hip replacements.
MicroPort OrthopedicsSep 18, 2017 - Lower riskMedical device
Siemens Medical Solutions USA, Inc. recalls Torque wrench used on the bolts for the Symbia T2 model 10275008, Symbia Intevo Excel model 10764801, Symbia Intevo 16
Siemens recalls torque wrenches for Symbia T2, Intevo, and Evo models due to being out of tolerance during installation. Affected units include specific serial numbers and models. No remedy is stated in the recall notice.
Siemens Medical SolutionsSep 18, 2017 - Lower riskMedical device
Becton Dickinson & Company recalls BD Vacutainer¿ Barricor" Lithium Heparin Plasma Blood Collection Tubes for Invitro Diagnostic Use, Catalog Numbers:
Recalled BD Vacutainer Barricor Lithium Heparin Plasma Blood Collection Tubes (Catalogs 365043-365047) have increased residual blood on stoppers after use, potentially affecting test accuracy. Contact BD for details.
Becton DickinsonSep 18, 2017 - UnratedFood
Cargill Salt recalls Cargill Sea Salt Tablets; Net Wt. 50 lbs. (22.7 kg) cardboard case. 40 grain salt tablets; Ingredients: Salt Cargill
Cargill recalls 50-lb sea salt tablets with metallic fragments. Stop using if you have batch 10215ADBAA or 10915ADBAA. No remedy provided in official notice.
Cargill SaltSep 18, 2017 - Stop using nowFood
Death Wish Coffee Company, LLC recalls Death Wish Nitro Canned Cold Brew Coffee 11 oz UPC: 851552005599
Death Wish Coffee recalls 11oz Nitro Cold Brew Coffee with potential Clostridium Botulinum risk. Consumers should check UPC 851552005599 for affected products.
Death WishSep 18, 2017 - Stop using nowFood
J R Simplot Co Corporate HQ recalls Simplot Traditional Tater Gem. Net Wt. 30 lb. (13.6 kg), foodservice corrugated case, 6/5 lbs. clear poly bags per
J R Simplot Co recalls Traditional Tater Gem due to rigid plastic pieces. Check lot code 420AUG071703 and distribution states.
SimplotSep 18, 2017 - Lower riskFood
Grand Supercenter Inc. recalls HAIOREUM, RICE POP SNACK, KOREAN STYLE SNACK 0.41 LBS (190 G)
Grand Supercenter recalls Haioreum Rice Pop Snack (0.41 lbs) after reports of wheat allergy reactions. Consumers should avoid this product if they have wheat allergies.
Grand SupercenterSep 18, 2017 - Lower riskMeat & poultry
German Sausage Haus, LLC, Recalls Meat Products Due To Possible Processing Deviation and Staphylococcal Enterotoxin Contamination
USDA FSIS recalls 1,252 pounds of German Sausage Haus smoked meats from June to September 2017 due to possible staphylococcal enterotoxin contamination from processing deviations.
German Sausage HausSep 17, 2017 - Use cautionVehicle
MINI CLUBMAN (2018) recall — Trailer Hitches
Curt is recalling 2016-2018 Mini Clubman vehicles with certain trailer hitches that may sag or separate under load, increasing crash risk. Owners should contact Curt for a free replacement.
CurtSep 17, 2017 - Use cautionMeat & poultry
America New York RI Wang Food Group Recalls Sausage Products Due To Misbranding and an Undeclared Allergen
USDA recalls 53,973 pounds of pork sausages from 2016-2017 due to milk allergen not declared on labels. Consumers urged not to consume.
China BrandSep 15, 2017 - Use cautionVehicle
INFINITI Q50 (2017) recall — Air Bags
Nissan is recalling 2017 Infiniti Q50 vehicles with driver air bag inflator that may crack during crash, increasing injury risk. Owners must have inflator replaced free by dealers.
InfinitiSep 15, 2017 - Use cautionVehicle
FOREST RIVER VIBE (2018) recall — Equipment
Forest River recalls 2018 Vibe trailers with potential LP line damage causing propane leaks and fire risk. Owners must get free LP line replacement by dealers.
Forest RiverSep 15, 2017 - Lower riskMedical device
Cepheid recalls Xpert EV Assay, Catalog GXEV-100N-10. The Cepheid Xpert EV assay is a reverse transcription polymerase chain reaction
Cepheid recalls Xpert EV Assay (GXEV-100N-10) due to higher than expected invalid test results in CSF samples for meningitis diagnosis.
CepheidSep 15, 2017 - Use cautionMedical device
Covidien LLC recalls Endo GIA" Radial Reload with Tri-Staple" Technology The Endo GIA radial reloads with Tri-Staple Technology have
Covidien recalls Endo GIA Radial Reload with Tri-Stap: Cartridge disengagement due to manufacturing error. Affected units have product number EGIARADXT and lot code N6L0351X.
CovidienSep 15, 2017 - Lower riskMedical device
Hologic, Inc recalls Panther(R) System, Catalog Number 902615, For Use with Hologic Assays, For In Vitro Diagnostic Use
Hologic recalls Panther System (Catalog 902615) for potential incorrect test results due to an incorrect incubator installation. Affected units have serial number 20900001124.
HologicSep 15, 2017 - Lower riskMedical device
Zimmer Biomet, Inc. recalls 36MM COCR MODULAR HD -6MM
Zimmer Biomet recalls 36MM COCR MODULAR HD -6MM implants with incorrect etching that affects function. Affected units have lot number 236840. Stop using if you own this model.
Zimmer BiometSep 15, 2017 - Use cautionMedical device
HILL-ROM MANUFACTURING, INC. recalls Monarch Airway Clearance System, Model 1000, Product Numbers: PMACS1NA (has blue tooth capability only) and PMACS1WI
Hill-Rom recalls Monarch Airway Clearance System Model 1000 with specific serial numbers due to electromagnetic interference risk for pacemakers and defibrillators.
Hill-RomSep 15, 2017 - Lower riskMedical device
Encore Medical, Lp recalls EMPOWR PS KNEE(TM) e+, REF 343-19-707, SIZE 7, 19mm, QTY 01, GREY, STERILE Product Usage The EMPOWR PS Inserts are
Encore Medical recalls EMPOWR PS Knee e+ inserts (REF 343-19-707) due to incorrect packaging with a different implant model. Affected units may have safety risks from mismatched components.
Encore MedicalSep 15, 2017 - Lower riskDrug
Baxter Healthcare Corporation recalls Intralipid 20%, A 20% I.V. Fat Emulsion, 100 ml bag, Rx only, Manufactured by Fresenius Kabi, Uppsala, Sweden for
Baxter Healthcare recalls Intralipid 20% IV fat emulsion (100ml) due to potential exposure to subfreezing temperatures during transit, which may affect product safety.
Baxter HealthcareSep 15, 2017 - Lower riskDrug
Becton Dickinson & Company recalls ChloraPrep OneStep (Clear) (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA)), 3 mL applicator,
Becton Dickinson recalls ChloraPrep OneStep Clear solution due to incorrect labeling. The product is labeled as 'Chloroprep Onestep (Clear)' but should be 'Chloroprep with Tint (Hi Lite Orange)'. This labeling error may cause confusion with a different product.
Becton DickinsonSep 15, 2017 - Stop using nowDrug
Gadget Island, Inc recalls grande X 5800 capsule, (Maca Root 120 mg, Horny Goat Weed 120 mg, Guarana Seed 80 mg, Ginko Leaf 60 mg, Saw Palmetto
Gadget Island recalls grande X 5800 capsules containing undeclared drugs. These supplements may contain sildenafil, desmethyl carbodenafil, and tadalafil without approval.
Gadget IslandSep 15, 2017 - Lower riskFood
Dr. Pepper Snapple Group Inc recalls Diet Rite, Pure Zero Cola, 0 calories, 0 caffeine, 0 sodium, Bottled under the authority of Dr. Pepper/Seven up Inc.
Dr. Pepper Snapple Group recalls Diet Rite and Pure Zero Cola products labeled as caffeine-free but containing caffeine. Consumers should check bottle codes for affected items.
Dr. Pepper Snapple GroupSep 15, 2017 - Lower riskFood
KIND LLC recalls KIND Dark Chocolate Nuts and Sea Salt Bar-containing 12 /1.4 oz (40 g) bars Box :16.08 oz (480 g) per pack. Box UPC:
KIND LLC recalls 12-pack of Dark Chocolate Nuts and Sea Salt bars due to missing walnut allergen label on outer box. This poses a risk for people with walnut allergies. No action needed as the bars themselves are labeled.
KINDSep 15, 2017 - Lower riskFood
Pro Bioteks Laboratories recalls Bio35, Vitamin-Mineral Omega Oils Trace Minerals Dietary Supplement, 100 Softgel Capsules. UPC 0-26341-12900-2
Pro Bioteks recalls Bio35 dietary supplement due to undeclared soy lecithin. Consumers should check product details and contact the company for guidance.
Pro BioteksSep 15, 2017 - Use cautionVehicle
PIERCE ARROW XT (2016) recall — Steering
Pierce is recalling 2016 Arrow XT vehicles with potentially loose steering tie rods that could cause loss of steering and crash risk. Affected owners should contact Pierce for free inspection or replacement.
PierceSep 14, 2017 - Stop using nowVehicle
CHEVROLET SILVERADO 3500 (2018) recall — Seat Belts
GM recalls certain 2017-2018 Chevrolet Silverado 2500/3500 trucks due to incorrect torsion bars in front seat belt retractors. Free dealer repair available.
ChevroletSep 14, 2017 - Use cautionMedical device
Smith & Nephew, Inc. recalls smith&nephew LEGION L-WEDGE, 10 MM DIS X 5 MM POS, SIZE 4, SCREW-ON FEMORAL WEDGE, REF 71421733, STERILE R Product The
Smith & Nephew recalls Legion L-Wedge Size 4 knee implants with 5mm screws instead of required 10mm screws. This mismatch risks improper joint fixation during surgery.
Smith & NephewSep 14, 2017 - UnratedMedical device
C.R. Bard, Inc. recalls HydroSil Gripper Intermittent Catheters- 10" lengths - 30 catheters per box, each catheter is packaged in an individual
C.R. Bard recalls 10" HydroSil Gripper intermittent catheters (30 per box) due to potential catheter cutting during use. Affected lots include JUBT0404, JUBP0700, JUBR2498, JUBS1289. No remedy specified in recall notice.
C.R. BardSep 14, 2017 - Lower riskMedical device
Cardiovascular Systems Inc recalls Peripheral Diamondback 1.50 Solid OAD, a percutaneous orbital atherectomy system indicated for use as therapy in
Cardiovascular Systems recalls Diamondback 1.5:0 Solid OAD devices due to potential labeling mix-up in two production lots. Affected units may have incorrect labeling, but no safety hazard is reported.
Cardiovascular SystemsSep 14, 2017
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