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
35,021 found- Lower riskMedical device
Skytron, Div. The KMW Group, Inc recalls VGDF-SKY (R4-010-06) VGA TO FIBER CONVERTER-Single Format Faceplate, a component of the SkyVision Linx 300 Integration
Skytron recalls VGDF-SKY (R4-010-06) VGA to Fiber Converter for potential video signal failure in SkyVision Linx 300 systems. Affected units may lose video display on secondary screens.
SkytronSep 11, 2020 - Use cautionMedical device
Bien-Air Surgery Sa recalls Bien-Air Surgery REF 1600517-001 SN ******* MULTIFUNCTION PEDAL OSSEODUO - Product Usage: Product Usage: intended to
Recall of Bien-Air Surgery OSSEODUO multifunction pedal models with serial numbers starting 18F0017-19E0069. Magnet may detach and cause unattended motor start without user control.
Bien-Air SurgerySep 11, 2020 - Lower riskDrug
Genesis Partnership Company SA recalls Genesis Hand Sanitizer Gel, Topical Solution, Non Sterile Solution, 1 gallon (3785 mL) bottle, Manufactured by Genesis
Genesis recalls 1-gallon hand sanitizer gel due to manufacturing in a facility with sub-potent ethanol levels, potentially reducing effectiveness.
GenesisSep 11, 2020 - Use cautionConsumer product
Medique Recalls 31 Different Over-the-Counter Drugs Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning; Sold Exclusively on Amazon.com (Recall Alert)
Medique recalls 31 OTC drugs sold on Amazon since June 2018 that lack child-resistant packaging, posing poisoning risk to young children. Consumers should store out of reach and contact for refund.
MediqueSep 11, 2020 - Lower riskMedical device
Blue Ortho recalls Instructions For Use document of the GPS Trackers.
Blue Ortho recalls specific GPS Tracker models (A100003, A100004, A100005, A100006) due to potential language issues in reprocessing instructions. Affected units have listed serial numbers.
Blue OrthoSep 10, 2020 - Use cautionMedical device
Tandem Diabetes Care Inc recalls t:slim X2 Insulin Pump with Dexcom G5 Mobile CGM, and t:slim X2 Insulin Pump with Basal-IQ Technology
Tandem Diabetes Care recalls t:slim X2 insulin pumps with Dexcom G5 or Basal-IQ tech due to potential battery fluctuations causing insulin delivery to stop, risking hyperglycemia.
Tandem Diabetes CareSep 10, 2020 - Stop using nowConsumer product
Residential Elevators Recalls Elevators Due to Impact Hazard (Recall Alert)
Recalled residential elevators (models LLT-952-955, installed 2014-2017) may rise unexpectedly, risking injury. Consumers must stop using and contact for free repair.
Residential ElevatorsSep 10, 2020 - Use cautionConsumer product
Organic Aromas Recalls Wintergreen Essential Oil Due to Failure to Meet Child Resistant Packaging Requirements; Risk of Poisoning (Recall Alert)
Organic Aromas Wintergreen Essential Oil lacks child-resistant packaging, risking poisoning for young children. Consumers should store out of reach and get store credit or replacement.
Organic AromasSep 10, 2020 - Use cautionVehicle
JAYCO GREYHAWK (2019) recall — Equipment
Jayco is recalling 2016-2019 Greyhawk motorhomes due to hydraulic pump and reservoir detachment risk when contacting ground, potentially causing crashes. Owners must have support bracket installed by dealers.
JaycoSep 9, 2020 - Use cautionVehicle
JAYCO EMBARK (2020) recall — Electrical System
Jayco is recalling 2019-2020 Embark motorhomes due to a damaged circuit board that could cause fire. Owners must contact Jayco for free over-current protection installation.
JaycoSep 9, 2020 - UnratedMedical device
W L Gore & Associates, Inc. recalls GORE TAG CONFORMABLE Thoracic Stent Graft with ACTIVE CONTROL System
W L Gore recalls thoracic stent grafts with ACTIVE CONTROL System due to deployment failure risk. Affected models include TGM212110X* through TGMR404020X* with specific catalog numbers.
W L GoreSep 9, 2020 - Use cautionMedical device
W L Gore & Associates, Inc. recalls GORE TAG Conformable Thoracic Stent Graft with ACTIVE CONTROL System
W L Gore recalls conformable thoracic stent grafts with Active Control System due to delivery catheter connection preventing removal. Affected units include specific catalog numbers and all lot numbers. Consumers should contact for details.
W L GoreSep 9, 2020 - Lower riskMedical device
Encore Medical, LP recalls EMPOWR Acetabular System *** EMPOWR Acetabular Cup, Cluster Hole, 54G *** Size 54G 54 mm Dia./Cluster Hole Alpha Code G
Encore Medical recalls EMPOWR Acetabular Cup (Size 54G) due to incomplete machining causing a protruding peg that may lead to improper seating. Affected patients should contact for details.
Encore MedicalSep 9, 2020 - Lower riskMedical device
Ethicon, Inc. recalls VICRYL MONOFILAMENT VIOLET 4IN (10CM) USP 10-0 (M0.2) SINGLE-ARMED CS140-6 - Product Usage: Intended for ophthalmic
Ethicon recalls VICRYL monofilament sutures that may have wrong size (6-0 vs 10-0) for eye surgery. Incorrect sutures could lead to improper wound closure. Affected products sold between 2020-2024.
EthiconSep 9, 2020 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Uroskop Omnia, Model no. 10094910 - Product Usage: a solid state detector fluoroscopic X-ray system, primarily for
Siemens recalls Uroskop Omnia model 10094910 X-ray systems due to risk of support arm dislodging after prolonged intense use. Affected units have specific serial numbers.
SiemensSep 9, 2020 - Use cautionMedical device
Smith & Nephew, Inc. recalls OSTEORAPTOR 2.3 W. UB COBRAID BLUE-Absorbable Suture anchor Product Number: 72201993
Smith & Nephew recalls OSTEORAPTOR 2.3W absorbable suture anchors with batch numbers 2012768-2056307 due to potential pouch seal failure causing sterile contamination during surgery.
Smith & NephewSep 9, 2020 - Lower riskDrug
PAI Holdings, LLC. dba Pharmaceutical Associates Inc recalls Citalopram Oral Solution, USP 20 mg/10 mL, 10 mL unit dose cups, Rx Only, Mfg for: Pharmaceutical Associates, Inc.
Pharmaceutical Associates recalls 20 mg/10 mL citalopram oral solution due to impurities and degradation at 9 months. Affected lots expired by April 2021. Consumers should contact pharmacy for safe alternatives.
Pharmaceutical AssociatesSep 9, 2020 - Stop using nowDrug
MEDEK LLC recalls M Hand Sanitizer Ethyl Alcohol Antiseptic 80%v/v, Topical Solution 128 oz/3,785 mL, Made in Mexico by: Grupo
MEDEK recalls 128 oz hand sanitizer due to methanol contamination and subpotent ethanol. FDA analysis found unsafe levels of methanol and insufficient alcohol content. Consumers should stop using affected products immediately.
MEDEKSep 9, 2020 - Use cautionDrug
P & L Developments, LLC recalls Nicotine Gum, Nicotine Polacrilex Gum USP, 2 mg (nicotine), 110-count pieces per carton, Distributed By: Rite Aid, 30
P & L Developments recalls Nicotine Gum 2 mg distributed by Rite Aid due to incorrect package inserts. Check your lot number and expiration date.
P & L DevelopmentsSep 9, 2020 - Lower riskFood
Lidl US TRADING recalls Lidl Organic Butter Microwave Popcorn, 3 x 3.3oz, 10 boxes per case and 3 popcorn bags per box .
Lidl recalls organic butter microwave popcorn due to foreign material in some batches. Affected items have specific best by/lot codes. Consumers should check their packaging for these codes and contact Lidl for details.
LidlSep 9, 2020 - Lower riskFood
Shatto Milk Co recalls Shatto Milk Company, Brownie, Chocolate Brownie and Vanilla Ice Cream Sammich, Net Wt. 5 oz, Shatto Milk Company,
Shatto Milk Co recalls 5oz ice cream sandwiches due to undeclared soy lecithin in the cookie portion, posing a risk for soy-allergic individuals.
Shatto Milk CoSep 9, 2020 - Use cautionFood
Gilster-Mary Lee Corp. recalls Microwave popcorn packaged in the following ways: 1) Full Circle Organic Microwave Popcorn Salted, 3-2.9 oz (82 g)
Full Circle Organic Microwave Popcorn Salted bags (3-2.9 oz) recalled due to small glass particles that could cause injury. Consumers should check UPCs and stop using affected products.
Full CircleSep 9, 2020 - Stop using nowConsumer product
WHILL Recalls WHILL Personal Electric Vehicles Due to Crash and Injury Hazards
WHILL recalls Model Ci personal electric vehicles due to control pad malfunction causing crashes and injuries. Affected units have serial numbers from C_17111: C_1909011_US. Consumers should stop using and get a free replacement pad.
WHILLSep 9, 2020 - Stop using nowConsumer product
Royal Gourmet Recalls Deluxe Gas Grills Due to Fire Hazard; Sold Exclusively at Wayfair.com
Royal Gourmet recalls 2-burner propane gas grills (models GG2004-2006) sold online due to fire risk from melting plastic regulator hose. Consumers must stop using and contact for free repair kit.
Royal GourmetSep 9, 2020 - Use cautionConsumer product
Cycling Sports Group Recalls Front Racks for Cannondale Treadwell Bicycles Due to Fall Hazard
Cycling Sports Group recalls front racks with bamboo trays for Cannond: Treadwell bicycles due to risk of sudden detachment causing falls. Consumers must stop using until repaired.
Cycling Sports GroupSep 9, 2020 - UnratedMedical device
CooperSurgical, Inc. recalls MediCult Vitrification Cooling Media, Model Number 12284001F
CooperSurgical recalls MediCult Vitrification Cooling Media Model 12284001F due to label printing error showing wrong product type. Affected units sold in 2023 with specific lot number.
CooperSurgicalSep 8, 2020 - UnratedMedical device
GE Healthcare, LLC recalls System, Nuclear Magnetic Resonance Imaging - Product Usage: is a whole body magnetic resonance scanner designed to
GE Healthcare recalls specific MRI scanners due to potential electrical arc flash in the PGR cabinet. Affected models include 5148810-3, 5741000-100, 5741000-26, and 5741000-27. No remedy details provided in recall notice.
GE HealthcareSep 8, 2020 - Use cautionMedical device
ESAOTE S.P.A recalls AC/DC POWER SUPPLY for 7400, Part Number 151004301, XP Power Model Number AHM180PS19-XE1057, AC/DC Adapter associated
ESAOTE recalls AC/DC power supplies for specific ultrasound systems due to connector heating, smoke, and melting risks. Affected models include MyLabAlpha, MyLabGamma, and others with serial numbers below K17350001.
ESAOTESep 8, 2020 - Use cautionMedical device
Aesculap Implant Systems LLC recalls AESCULAP S4 Cervical Cross Connector L24mm, S4C CROSS CONNECTOR FIXED 24MM, product code SWT113T. Used in spinal fusion
Aesculap recalls S4 Cervical Cross Connectors (SWT113T) used in spinal fusion due to potential movement or microparticle abrasion. Affected patients should contact manufacturer for details.
Aescul: Aesculap Implant Systems LLCSep 8, 2020 - Lower riskFood
Ponder Foods recalls Pretty Thai brand Sweet Chili Sauce Net Wt 11.2 oz (317g) UPC 860043001224 packaged in a clear PET plastic bottle with
Ponder Foods recalls Pretty Thai brand Sweet Chili Sauce (11.2 oz) due to potential undeclared peanuts. Consumers should check UPC 860043001224 and lot number 0772000123 for affected items.
Ponder FoodsSep 8, 2020
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