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
34,960 found- Lower riskFood
Schrock's Sugar 'N Spice LLC recalls Maple Iced Cinnamon Rolls, Net Wt. 1.33 lbs., Walnuts on top in see-through clamshells with clear plastic lids. 8 rolls
Schrock's Sugar 'N Spice recalls 8-roll cinnamon rolls with undeclared walnuts. Consumers should check for see-through clamshells with clear plastic lids sold between July 2019 and August 2019.
Schrock's Sugar 'N SpiceAug 20, 2019 - Lower riskFood
Confectionery Arts International, LLC recalls All colors and sizes of Confectionery Arts International, LLC brand Jewel Dust, a pearlescent pigment, manufactured and
Recall of Jewel Dust pigment manufactured before April 25, 2019 due to borosilicate glass found in FDA samples. Consumers should check product codes and contact manufacturer for details.
Confectionery Arts InternationalAug 20, 2019 - Stop using nowFood
Whole Foods Market recalls Decorated Red Apple Cookies sold in display case in retail stores
Whole Foods Market recalls 4,880 decorated red apple cookies due to undeclared egg. Sold through Aug 20, 2019. Check your display case.
Whole Foods MarketAug 20, 2019 - Stop using nowConsumer product
Southwire Recalls Electrical Outlet Boxes Due to Fire Hazard
Garvin Pop-Up Floor Box Kits with stainless steel or brushed brass finishes may overheat and cause fire. Consumers must unplug devices, stop using, and get a refund from Southwire.
GarvinAug 20, 2019 - Use cautionConsumer product
SAMpark Recalls Children's Pajamas Due to Violation of Federal Flammability Standard
SAMpark recalls children's pajamas that fail federal flammability standards, risking burn injuries. Consumers must stop using and get a refund.
SAMparkAug 20, 2019 - Stop using nowConsumer product
Crate and Barrel Recalls Push Walkers Due to Choking and Laceration Hazards
Crate and Barrel recalls Activity Push Walkers with choking and laceration hazards due to exposed sharp parts. Consumers should stop using and get a refund.
Crate and BarrelAug 20, 2019 - Use cautionVehicle
HORTON TYPE I (2020) recall — Air Bags
Halcore is recalling 2018-2020 Horton Type I emergency vehicles due to air bags that may not inflate properly in crashes, increasing injury risk. Owners must contact Halcore for free replacement.
HalcoreAug 19, 2019 - Lower riskMedical device
OrthoPediatrics Corp recalls OrthoPediatrics Adolescent attachment bolt used with the Pediatric Nailing Platform (PNP) targeting arm- intended as an
OrthoPediatrics recalls adolescent attachment bolts used with Pediatric Nailing Platform for potential delay in surgical procedures. Learn about affected models and what to do.
OrthoPediatricsAug 19, 2019 - Lower riskMedical device
CooperSurgical, Inc. recalls LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.
CooperSurgical recalls LEEP Return Patient Pads with reversed expiration dates on outer boxes. This could lead to expired pads being used in procedures. Affected lots: 201809125 and 2: 201809135.
CooperSurgicalAug 19, 2019 - Lower riskMedical device
Intuitive Surgical, Inc. recalls da Vinci SP Camera; PN 430060-33; Model Number: 430060-33. For endoscopic surgery.
Intuitive Surgical recalls da Vinci SP Camera model 430060-33 due to residual soil on camera tips that could cause image issues or sensitization risks during surgery.
Intuitive SurgicalAug 19, 2019 - Lower riskMedical device
OrthoPediatrics Corp recalls Model No. 01-1503-0032 (Adolescent Nail Attachment Bolt). Component of the Pediatric Nailing Platform. Product Usage:
OrthoPediatrics recalls Adolescent Nail Attachment Bolt Model 01-1503-0032 due to potential binding with intramedullary nails, which may delay surgical procedures. Affected units include specific model numbers listed in the recall.
OrthoPediatricsAug 19, 2019 - Lower riskMedical device
Howmedica Osteonics Corp. recalls TRIATHLON FEMORAL DISTAL AUGMENT 15MM - SIZE 2 RIGHT Catalog # 5542-A-202 - Product Usage: Triathlon Femoral Distal
Howmedica recalls Triathlon Femoral Distal Augments with overhang issue that may protrude beyond mating component. Affected units include specific catalog numbers and lots. Contact for remedy.
HowmedicaAug 19, 2019 - Lower riskMedical device
Becton, Dickinson and Company, BD Biosciences recalls BD FACSLyric Flow Cytometer, 3-Laser 12 Color Instrument, REF: 663029, when using BD Trucount Tubes
BD Biosciences recalls BD FACSLyric Flow Cytometers (serial numbers listed) when used with BD Trucount Tubes due to potential false high cell counts affecting patient care decisions.
BD BiosciencesAug 19, 2019 - Use cautionMedical device
RESPIRATORY THERAPEUTICS GROUP LLC recalls RespVent Closed Suction System T-Piece Tracheostomy Adult, Diameter: 4.6mm (14F), Length: 30.5cm (12in.), MDI Adapter,
RespVent recalls adult tracheostomy suction systems with potential catheter disconnection risk. Affected units may cause suction failure or difficulty removing catheter from patient airway.
RespVentAug 19, 2019 - Use cautionFood
Bubbies Homemade Ice Cream and Desserts, Inc. recalls Bubbies Mochi Ice Cream -Chocolate Coconut Item Code CS812067, UPC Code 20203-5, UPC GTIN 10787325202032. Product is
Bubbies recalls chocolate coconut mochi ice cream due to potential plastic pieces. Consumers should check item codes and UPCs for affected products.
BubbiesAug 19, 2019 - Stop using nowConsumer product
Club Car Recalls Gas Utility and Transport Vehicles Due to Risk of Fuel Leak and Fire Hazard (Recall Alert)
Club Car recalls 2019 utility and transport vehicles with fuel leak risk causing fire. Owners must stop using and contact Club Car for free repair.
Club CarAug 19, 2019 - Stop using nowConsumer product
Club Car Recalls Gas Golf and Transport Vehicles Due to Fire and Burn Hazards (Recall Alert)
Club Car recalls 2019 gas-powered golf and transport vehicles with model numbers BX, BY, BQ, BS, BW, BJ, DF, DJ, AY, AW due to fuel leaks causing fire and burn risks. Owners must stop using and contact Club Car for free repairs.
Club CarAug 19, 2019 - Use cautionPet food
Chef Toby – Pig ears: Potential to be contaminated with Salmonella
Dog Goods is recalling Chef Toby Pig Ears treats due to possible Salmonella contamination. Consumers are urged to return products for a full refund.
Dog GoodsAug 16, 2019 - Use cautionVehicle
FOREST RIVER ROCKPORT (2019) recall — Equipment
Forest River recalls 2019 Rockport box vans with Uline Bulk Storage racks due to improper welding that may cause beams to fail when loaded, risking injury. Owners will receive free beam replacements.
Forest RiverAug 16, 2019 - Use cautionMedical device
Enztec Limited recalls REF 800-05-035, ENZTEC FEMORAL IMPACTOR - DJO, (01) 09421028110624 (10) 999999, To be used only with DJO EMPOWR 3D KNEE
Enztec recalls femoral impactors used with DJO EMPOWR 3D Knee due to higher risk of arm fracture during surgery, potentially causing delays or revision surgery.
EnztecAug 16, 2019 - Lower riskMedical device
IrriMAX Corporation recalls Irrisept Wound Debridement and Cleansing System. 12 units per case.
IrriMAX recalls 12 units per case of Irrisept Wound Debridement System due to potential sterile pouch seal defect risking lack of sterility. Affected units have specific catalog and lot numbers.
IrriMAXAug 16, 2019 - Lower riskDrug
SCA Pharmaceuticals, LLC recalls Ketamine 50 mg/5 mL in 0.9% Sodium Chloride Injection for IV or IM Use (concentration = 10 mg/mL), 6 mL Syringe, Rx
SCA Pharmaceuticals recalls Ketamine 50 mg/5 mL injection (NDC 70004-0430-09) due to lack of sterility assurance. This may cause infections if used improperly.
SCA PharmaceuticalsAug 16, 2019 - Lower riskFood
Abbott Nutrition, Division of Abbott Laboratories recalls Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 per carton.
Abbott Nutrition recalls Similac Pro-Sensitive 2 fl oz plastic bottles packed 12 per carton from a specific batch due to packaging mix-up with Pro-Advance bottles.
Abbott NutritionAug 16, 2019 - Lower riskFood
Kashat Wholesale, Inc. recalls Ground Cinnamon 4oz plastic container 24 containers per wholesale case
Kashat Wholesale recalls 4oz plastic cinnamon containers with lead detected in bulk cinnamon. Consumers should avoid using products with lot M-60445.
KashatAug 16, 2019 - Lower riskFood
Pepsico Inc recalls Diet Mountain Dew (Dewnited Michigan) 20 oz. plastic bottle Promotional give away as individual units
Pepsi recalls Diet Mountain Dew promotional bottles that actually contain full calories. Consumers should check labels for 'Dewnited Michigan' and use by date.
PepsiAug 16, 2019 - Stop using nowMeat & poultry
Tyson Foods, Inc. Recalls Weaver Brand Ready-To-Eat Chicken Patty Products due to Possible Foreign Matter Contamination
Tyson Foods recalls ~39,078 lbs of Weaver brand frozen chicken patties due to possible contamination with extraneous materials. Do not consume.
WeaverAug 15, 2019 - Stop using nowMedical device
Bioseal Corporation recalls Bioseal Trachea Extender 1/pl 50pk/Cs, REF TRAX01/50, LOT XXXX, STERILE EO, Single Use Only, Date of Manufacture XXXX,
Bioseal recalls trachea extenders with potential stress cracks causing breathing system leaks. Patients may not receive proper ventilation. Stop using immediately if you have the recalled model.
BiosealAug 15, 2019 - Lower riskMedical device
Western / Scott Fetzer Company recalls Grab n Go Opti series VIPR system Model # PRX-9646 - Product Usage: The Grab n Go Opti system is an integrated delivery
Western/Scott Fetzer recalls Grab n Go Opti VIPR system Model PRX-9646 due to limited access to flow settings from control knob rotation. This device is for emergency oxygen use only.
Western/Scott FetzerAug 15, 2019 - Lower riskMedical device
Musculoskeletal Transplant Foundation, Inc. recalls QuickGraft¿ Model # 430PST
Musculoskeletal Transplant Foundation recalls QuickGraft Model 430PST due to label measurements not accounting for tension, potentially increasing surgical time. Affected units have specific serial numbers listed.
Musculoskeletal Transplant FoundationAug 15, 2019 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Atellica IM 1300 Analyzer, (SW) version V1.19.0 and V1.19.2 Siemens Material Number (SMN): 11066001
Siemens Healthcare recalls Atellica IM 1300 analyzers with specific software versions due to scanning errors with new reagent lots. Affected units have Siemens Material Number 11066001 or UDI 00630414007960.
Siemens HealthcareAug 15, 2019
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