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- Lower riskFood
Water Gardens Confections LLC recalls Macey's Kong Popcorn, 24 oz., in plastic zip pouch. UPC: 0-41172-00046-7, Manufactured By: Water Gardens Confections,
Water Gardens Confections LLC recalls Macey's Kong Popcorn 24oz plastic pouches due to small plastic fragments found during packaging. Consumers should check UPC 0-41172-00046-7 for affected items.
Macey's Kong PopcornDec 18, 2020 - Lower riskFood
JR Simplot Company - Headquarters recalls SPUD-QUEEN LATTICE CUT - SKIN ON FROZEN POTATOES, master case SKU 10071179 041290. Distributed by Mid America Potato
JR Simplot recalls SPUD-QUEEN Lattice Cut Skin-On Frozen Potatoes (SKU 10071179) due to undeclared wheat. This foodservice product may contain wheat without labeling, posing a risk for those with wheat allergies.
JR SimplotDec 18, 2020 - Use cautionMeat & poultry
FSIS Issues Public Health Alert for Ready-to-Eat Pork Snack Stick Products Due to Misbranding and an Undeclared Allergen
FSIS public health alert: Country Meats HOT BBQ Flavor Smoked Pork Snack Sticks may contain undeclared milk allergen. Consumers with dairy allergies should not consume these products.
Country MeatsDec 17, 2020 - Use cautionVehicle
FORD E-350 (2021) recall — Engine
Ford recalls 2021 E-350 vehicles with potential engine cover overheating causing burns. Owners must have engine cover inspected for gaps and get free insulation patches.
FordDec 17, 2020 - Use cautionVehicle
JAYCO SENECA (2020) recall — Equipment
Jayco is recalling 2015-2020 Seneca Class C motorhomes due to potential hydraulic pump and reservoir detachment causing leaks and crash risks. Affected owners should contact Jayco for a free bracket fix.
JaycoDec 17, 2020 - Use cautionVehicle
HONDA ACCORD HYBRID (2020) recall — Electrical System
Honda is recalling certain 2020 Accord Hybrids due to potential power loss that could increase crash risk. Owners will receive free software updates to fix the electrical issue.
HondaDec 17, 2020 - Stop using nowVehicle
FORD EXPLORER (2020) recall — Engine
Ford recalls certain 2020-2021 Explorers due to loose motor mount fasteners that may disconnect the axle, causing loss of power and crash risk.
FordDec 17, 2020 - Use cautionVehicle
FORD ECOSPORT (2020) recall — Air Bags
Ford is recalling 2020 EcoSport vehicles with air bags that may not deploy properly in crashes, increasing injury risk. Owners must have air bag modules replaced free by dealers.
FordDec 17, 2020 - Stop using nowVehicle
CHEVROLET SILVERADO 2500 (2020) recall — Seat Belts
GM recalls certain 2020 Chevrolet Silverado 2500 vehicles due to unsecured front-row center seat belt brackets. Check your VIN for details.
ChevroletDec 17, 2020 - Lower riskMedical device
Roche Diagnostics Operations, Inc. recalls A calculator/data processing module for clinical use is an electronic device intended to store, retrieve, and process
Roche recalls Cobas Infinity calculators for clinical use due to a software error that may remove serum indices flags, risking unreliable test results. Affected units include all versions from cobas infinity 3.00.0:00 onwards.
RocheDec 17, 2020 - Lower riskMedical device
Bioventus, LLC recalls EXOGEN Ultrasound Coupling Gel
Bioventus recalls EXOGEN Ultrasound Coupling Gel with potential microbial particulates. Affected units include specific part numbers and lots. Consumers should check their product details and contact Bioventus for guidance.
BioventusDec 17, 2020 - Lower riskMedical device
Fresenius Medical Care Holdings, Inc. recalls Fresenius Medical Care NaturaLyte Liquid Acid concentrate-Liquid Acid Concentrate for Bicarbonate Hemodialyis Part
Fresenius Medical Care recalls NaturaLyte Liquid Acid concentrate for bicarbonate hemodialysis due to missing product labels. Affected units have part number 08-3251-9 and lot code 20NTAC040.
Fresenius Medical CareDec 17, 2020 - Use cautionMedical device
GE Healthcare, LLC recalls System, X-Ray, Tomography, Computed: Revolution CT, Revolution CT ES.
GE Healthcare recalls Revolution CT, Revolution CT ES and related systems due to potential missing/damaged table pinch protectors that could cause lacerations from exposed table screws.
GE HealthcareDec 17, 2020 - Stop using nowDrug
NDAL Mfg Inc. recalls ManukaGuard Medical Grade Manuka Honey Allercleanse Nasal Spray, 1.3 FL OZ (40mL) bottle, 270 measured sprays,
NDAL Mfg Inc. recalls ManukaGuard Medical Grade Manuka Honey Allercleanse Nasal Spray due to yeast contamination. Check your lot number and expiration date.
ManukaGuardDec 17, 2020 - UnratedDrug
Ascend Laboratories LLC recalls Ascend Laboratories, llc Cephalexin for Oral Suspension, USP 250 mg per 5 mL 200 ml (when mixed) Rx Only Manufactured
Ascend Laboratories recalls 250mg/5mL cephalexin oral suspension (NDC 67877-545-68) due to failed impurity specifications. Rx-only product manufactured in India, distributed in US. No remedy stated in official notice.
Ascend LaboratoriesDec 17, 2020 - Use cautionDrug
Fresenius Kabi USA, LLC recalls Ketorolac Tromethamine Injection, USP, 60 mg per 2 mL (30 mg per mL), packaged in 2 mL Single Dose Vial, Rx only,
Fresenius Kabi recalls Ketorol: 60mg/2mL injection vials due to particulate matter found in reserve samples. This may cause serious injury if injected.
Fresen: KabiDec 17, 2020 - Use cautionDrug
CIPLA recalls Esomeprazole Magnesium for Delayed-Release Oral Suspension 40mg, packaged in unit dose packets, Rx only, Manufactured
Cipla recalls unit dose packets of Esomeprazole Magnesium 40mg due to cross-contamination with theophylline. Check your lot numbers and expiration date.
CiplaDec 17, 2020 - Lower riskDrug
Imprimis NJOF, LLC recalls Dexamethasone - Moxifloxacin PF Injection (1/5) mg/mL, Imprimis Rx Volume: 1mL/vial, Imprimis NJOF, LLC. 1705 Route 46
Imprimis recalls 13 vials of Dexamethasone-Moxifloxacin injection due to faulty crimps causing potential contamination. Affected lots: 20JUN010 (expiring 5/12/21).
ImprimisDec 17, 2020 - Lower riskDrug
SCA Pharmaceuticals recalls HYDROmorphone HCl 10mg/50mL in 0.9% Sodium Chloride Injection, CII, Rx Only, 50 mL Single Dose Syringe, SCA
SCA Pharmaceuticals recalls 50mL hydro morphine syringes due to potential sterility issues. Affected lots have specific barcodes and expiration dates. Consumers should contact the company for details.
SCA PharmaceuticalsDec 17, 2020 - Lower riskFood
O & H DANISH BAKERY recalls O H Danish Bakery Almond Danish Kringle, UPC 67209-00006. Net Weight: 24 oz. (1 lb. 8 oz) 680.3 grams
O & H Danish Bakery recalls Almond Danish Kringle due to possible undeclared pecans. Check UPC 67209-00006 for affected products.
O & H Danish BakeryDec 17, 2020 - Stop using nowConsumer product
Otis Elevator Company Recalls to Inspect Private Residence Elevators Due to Entrapment Hazard; Risk of Serious Injury or Death to Young Children
Otis and CemcoLift private residence elevators made before 2012 may trap young children, causing serious injury or death. Consumers must disable child access and schedule free inspections.
OtisDec 17, 2020 - Stop using nowVehicle
VOLKSWAGEN BEETLE (2014) recall — Air Bags
Volkswagen recalls certain 2012-2014 Beetle vehicles due to air bag inflators that may explode, causing serious injury or death. Free replacement available.
VolkswagenDec 16, 2020 - Use cautionVehicle
AUDI Q3 (2020) recall — Service Brakes, Hydraulic
Volkswagen recalls 2020 Audi Q3 vehicles with a brake pedal plate that can bend or detach during sudden stops, increasing crash risk. Owners must have brake pedal inspected and repaired free by dealers.
AudiDec 16, 2020 - Lower riskMedical device
Microbiologics Inc recalls KWIK-STIK 2 Pack, Catalog #0894P; KWIK-STIK 6 Pack, Catalog #0894K; and LYFO DISK, Catalog #0894L; Microsporum canis
Microbiologics recalls KWIK-STIK 2-Packs, 6-Packs, and LYFO DISK due to contamination with S. epidermidis. Affected items have specific catalog numbers and expiration dates.
MicrobiologicsDec 16, 2020 - Use cautionMedical device
Cook Medical Llc recalls Disposable Humidification Flask, Reference Part Number K-MINC-CTS-S, Order Number G32707
Cook Medical recalls Disposable Humidification Flasks (Reference Part Number K-MINC-CTS-S) due to a manufacturing defect that may cause silicone stoppers to dislodge or gas leaks, impairing incubator function.
Cook MedicalDec 16, 2020 - Lower riskMedical device
Microbiologics Inc recalls KWIK-STI(TM), GBS QC Set (Live Culture), REF 0243U. Specifically affected component: KWIK-STIK(TM), Lactobacillus
Microbiologics recalls KWIK-STI GBS QC Set (Live Culture) with incorrect expiration date label on negative control component. Affected units have expiration date labeled as 7/31/2020 instead of 7/31/2022. No action required per recall details.
MicrobiologicsDec 16, 2020 - Use cautionMedical device
Medtronic Neurosurgery recalls REF 27219-2 X1, Medtronic, Delta Valve, Neonatal, Performance Level 2.0, CE 0344, Sterile EO - Product Usage: Neonatal
Medtronic recalls neonatal Delta Valve shunt components due to potential shunt malfunction from improper valve connection. Affected units have a shorter ventricular catheter connection site than designed.
MedtronicDec 16, 2020 - Lower riskMedical device
Philips Ultrasound Inc recalls Philips EPIQ Diagnostic Ultrasound System; Model Numbers: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 7G, EPIQ 7C, EPIQ CVx &
Philips recalls EPIQ Elite, 5G, 5C, 7G, 7C, CVx & CVxi ultrasound systems due to Image Boost feature causing inaccurate blood flow visualization in certain transducers.
PhilipsDec 16, 2020 - Lower riskDrug
US Compounding Inc recalls Succinylcholine Chloride PF Inj. 200 mg/10 mL, 10 mL single use syringes, Rx only, US Compounding, 1270 Don's Lane,
US Compounding Inc recalls 200 mg/10 mL single-use syringes due to illegible lot and expiration dates on labels. This could lead to medication errors if the correct date is not verified.
US Compounding IncDec 16, 2020 - Lower riskFood
Bonduelle Canada Inc. recalls HRV Carrot.Cubes 1/20LB/HRV DCD Cartos 1/20LB - bag in box product in a corrugated case; IQF Cartotte Cubes 3/8"
Bonduelle Canada recalls carrot cubes products that may contain metal fragments. Consumers should check UPCs and lots for affected items. No remedy specified in recall notice.
Bondu: CanadaDec 16, 2020
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83,613 recalls tracked · 72,041 explained in plain English · 10,977 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.