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
35,025 found- Use cautionMedical device
Philips North America recalls (1) Ingenia Ambition X (Product Number 781356); (2) Ingenia Ambition S (Product Number 781359)
Philips recalls Ingenia Ambition X and S MRI scanners with serial numbers 47000-47200 and 48000-48200 due to risk of uncontrolled shutdown if power fails, potentially causing safety issues.
PhilipsJul 15, 2021 - Lower riskMedical device
Smiths Medical ASD Inc. recalls Pneupac paraPac plus 300 ventilator kit, REF P300NGB
Smiths Medical recalls Pneupac paraPac Plus 300 ventilator kits with duplicate serial numbers. This may cause confusion in identification and potential safety risks.
Smiths MedicalJul 15, 2021 - Lower riskMedical device
Beckman Coulter Inc. recalls Normand Remisol Advance Data Manager, REF: C69412, C69413, C44703, and C57017 is a software device that interfaces
Beckman Coulter recalls Normand Remisol Advance Data Manager software versions 2.0 and 2.1 due to potential for adding extra cells to patient requests, which could cause incorrect lab results. Affected units include specific reference numbers.
Beckman CoulterJul 15, 2021 - Use cautionDrug
API Solutions Inc. recalls Estriol USP41 Micro 25 Grams, Distributed by: A.P.I. Solutions 25309 Friendship Rd Daphne, AL Distributed by: Syntec
API Solutions Inc. recalls Estriol USP41 Micro 25 Grams distributed by Syntec Pharma Corp due to current Good Manufacturing Practice deviations.
API SolutionsJul 15, 2021 - Lower riskFood
Amys Kitchen Inc recalls Amy's Bowls, Tortilla Casserole & Black Beans; Made with organic tomatoes & Black Beans. NET WT 9.5 oz. (269g); gluten
Amy's Kitchen recalls tortilla casserole bowls made with organic tomatoes and black beans due to potential rubber gasket pieces in the product. This recall is for items purchased between April 2023 and the best before date.
Amy's KitchenJul 15, 2021 - Lower riskFood
BLUE ROBINS INC recalls Choujuki White Bread 6 slices: Net Wt. 13.9 oz. (374g) Ingredients: White Flour, Sugar, Margarine, Yeast Extract, Salt,
Blue Robins recalls Choujuki White Bread 6-slice packs due to improper allergen labeling that fails to declare milk as a potential ingredient in margarine.
Blue RobinsJul 15, 2021 - Stop using nowFood
Bright Farms recalls BrightFarms Mighty Romaine; packaged in clear, plastic clamshells; 4oz and 8oz; grown at the company's Rochelle,
Bright Farms recalls Mighty Romaine lettuce with possible Salmonella contamination. Products sold in clear plastic clamshells, 4oz and 8oz, with UPCs 5706200452 and 5706200491. Stop using immediately if you have these items.
Bright FarmsJul 15, 2021 - Stop using nowConsumer product
Real Flame Recalls Arroyo and Hideaway Wood Burning Fire Pits Due to Fire Hazard; Sold Exclusively at Crate and Barrel (Recall Alert)
Real Flame recalls Arroyo and Hideaway wood burning fire pits due to a fire hazard. Stop using them immediately and contact Real Flame for a full refund.
Real FlameJul 15, 2021 - Use cautionMedical device
Ostial Corporation recalls FLASH Ostial System, Dual Balloon Angioplasty Catheter, REF: OAB6014BA
Ostial recalls dual-balloon angioplasty catheters with potential deflation issues causing access site complications. Affected units include REF: OAB6014BA, Lot: 82210399.
OstialJul 14, 2021 - Use cautionMedical device
Smith & Nephew Orthopaedics Ltd. (Aurora) recalls smith&nephew BHR SQUARE HEADED NAIL, REF CATALOG NUMBER 999908. For use during orthopedic surgery.
Smith & Nephew recalls BHR Square-Headed Nails (Catalog 999908) used in orthopedic surgery due to risk of nail head detachment during procedures. Affected items have specific lot codes.
Smith & NephewJul 14, 2021 - Use cautionMedical device
Maquet Medical Systems USA recalls Heater Cooler Unit (HCU 30) The device supplies temperature-controlled water for cardioplegia heat exchangers and for
Maquet recalls HCU 30 Heater Cooler Units due to potential bacterial contamination, including Mycobacteria. Affected units have specific model numbers and serial numbers. Consumers should contact Maquet for details.
Maquet Medical SystemsJul 14, 2021 - Lower riskMedical device
Pentax of America Inc recalls Gastroscope Family # 1-Gastroscopes without a Water Jet Channel Models: EG-2790i, EG-1690K, EG-2490K, EG-2790K,
Pentax recalls certain gastroscopes made between April 2014 and May 2021 that lack a water jet channel, which could lead to improper cleaning and infection risks.
PentaxJul 14, 2021 - UnratedDrug
Qikmoov LLC recalls Vy&Tea (Vietnamese Labeling with a green leaf and a bird underneath) 15/KLT 45.0G (15 tea sachets per box),
FDA recalls Vy&Tea tea sachets (15 per box) due to unapproved sibutramine. Products marketed without FDA approval may pose health risks.
QikmoovJul 14, 2021 - UnratedDrug
Johnson & Johnson Consumer, Inc. recalls Neutrogena Invisible Daily defense body spray sunscreen BROAD SPECTRUM SPF 60+, Avobenzone (3%), Homosalate (10%),
Neutrogena Invisible Daily Defense body spray sunscreen with SPF 60+ is recalled due to cGMP deviations. Affected units may have quality issues affecting safety.
NeutrogenaJul 14, 2021 - Stop using nowConsumer product
Walgreens Recalls Disney Baby Winnie the Pooh Rattle Sets Due to Choking Hazard
Walgreens recalls Disney Baby Winnie the Pooh Rattle Sets due to feet detaching and posing a choking hazard for children under 3. Consumers should stop using and get a refund.
Disney BabyJul 14, 2021 - Stop using nowConsumer product
Academy Sports + Outdoors Recalls Ozone 500 Girls' and Boys' Elevate 24-Inch Bicycles Due to Fall and Injury Hazards
Academy Sports + Outdoors recalls Ozone 500 girls' and boys' 24-inch bicycles due to rear shock springs that can get stuck, causing pinches or sudden stops that lead to falls.
Academy Sports + OutdoorsJul 14, 2021 - Use cautionVehicle
FREIGHTLINER M2 (2017) recall — Exterior Lighting
Summit Bodyworks recalls one 2017 Freightliner M2-106 vehicle with overly bright rear LED lights that may cause vision issues for other drivers, violating FMVSS 108. Owners must contact customer service for a free filter kit.
Summit BodyworksJul 13, 2021 - Use cautionVehicle
ENTEGRA ANTHEM (2020) recall — Structure
Jayco recalls 2019-2021 Anthem RVs with Hehr 6400 windows for possible vent detachment during crashes or injuries. Free window inspections and repairs available.
JaycoJul 13, 2021 - Lower riskMedical device
Micro Therapeutics Inc, recalls EV3 Pipeline Flex Embolization Device with Flex Shield Technology
Micro Therapeutics recalls EV3 Pipeline Flex Embolization Device with Flex Shield Technology (PED2-250-10 to PED2-500-35) with specific lot numbers due to potential push wire fractures in the delivery system during use.
Micro TherapeuticsJul 13, 2021 - Use cautionVehicle
HYUNDAI IONIQ ELECTRIC (2019) recall — Electrical System
Hyundai is recalling 2017-2019 Ioniq electric vehicles due to potential unintended acceleration after gas pedal release, which could increase crash risk. Owners must contact Hyundai for free software update and wiring repair.
HyundaiJul 12, 2021 - Lower riskMedical device
Siemens Medical Solutions USA, Inc. recalls ACUSON Juniper Diagnostic Ultrasound System
Siemens recalls ACUSON Juniper ultrasound systems with intermittent power supply failures that cause inoperability. Affected units have specific serial numbers and firmware versions.
SiemensJul 12, 2021 - Use cautionMedical device
W. L. Gore & Associates Inc. recalls Gore Molding & Occlusion Balloon Catheter, REF Catalogue Number MOB37, SN XXXXXXXX, 10 mm - 37 m 10 Fr, Guidewire
W. L. Gore recalls specific balloon catheters for potential leakage during use, which could cause insufficient inflation or inability to inflate. Affected units have serial numbers between 22982051 and 23516741.
W. L. GoreJul 12, 2021 - Lower riskMedical device
Stanbio Laboratory, LP recalls Beta-Hydroxybutyrate Reagent A - Enzyme (unlabeled). in vitro diagnostic reagent.
Stanbio recalls unlabeled Beta-Hydroxybutyrate Reagent A enzyme for unstable quality control values. This in vitro diagnostic reagent may produce inaccurate test results if used improperly.
StanbioJul 12, 2021 - Use cautionMedical device
Abbott Laboratories, Inc recalls Alinity s System REF 06P16-01. An automated immunoassay analyzer for In Vitro diagnostic use in blood donor screening,
Abbott recalls Alinity s System REF 06P16-01 due to liquid waste pressure buildup that may spray users. Affected units have serial numbers AS1001 to AS1330.
AbbottJul 12, 2021 - Lower riskDrug
NATIVE PROMOTIONS, INC recalls QiYu Hand Sanitizer (ethyl alcohol 75% (v/v)), 16.9 FL OZ (500 ML) bottles, Manufactured by: Guangzhou Minghui
Native Promotions recalls QiYu hand sanitizer bottles with 75% alcohol that may not be strong enough for effective hand cleaning. Consumers should check product details and contact the company for guidance.
Native PromotionsJul 12, 2021 - Lower riskFood
NOW Health Group Inc. recalls Now Real Food Organic Steel Cut Oats, 2 lb bag, code 6295, UPC 733739062956, packed 8 bags per case; case packaging is
Now Real Food recalls 2lb organic steel cut oats with code 6295 due to potential organic beet sugar contamination. Consumers should check product codes and contact the company for details.
Now Real FoodJul 12, 2021 - Use cautionVehicle
BUICK ENCLAVE (2017) recall — Air Bags
General Motors recalls 2017 Buick Enclaves with driver air bag inflator explosion risk causing serious injury or death. Owners must have air bag module replaced free by dealer.
BuickJul 10, 2021 - Use cautionVehicle
TIFFIN PHAETON (2021) recall — Electrical System
Tiffin is recalling 2021 Phaeton RVs with an open electrical wire that could cause fire. Dealers will fix the issue free of charge.
TiffinJul 10, 2021 - Use cautionMedical device
PROCEPT BIOROBOTICS CORPORATION recalls AQUABEAM Handpiece, REF: HP2000, a sterile single-use component of the AQUABEAM Robotic System.
Procept recalls AQUABEAM HP2000 handpieces due to risk of tip detachment causing procedural delays. Affected units have specific lot numbers. Contact for replacement.
Procept BiometricsJul 9, 2021 - Lower riskMedical device
Copan Italia recalls COPAN FLOQSwabs, STERILE.EO, for drawing clinical samples. CE0123, for the following reference numbers REF:501CS01,
Copan recalls FLOQSwabs and STERILE.EO swabs due to sterility assurance failures from a contract sterilizer. These swabs may not be sterile, risking infections during clinical sampling.
CopanJul 9, 2021
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