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 riskMedical device
Fujifilm Medical Systems U.S.A., Inc. recalls Synapse Cardiovascular (Synapse CV). Software Versions: 6.0 to 6.2.1 The Synapse Cardiovascular image is a management
Fujifilm recalls Synapse Cardiovascular software versions 6.0 to 6.2.1 due to potential patient ID reuse during database merges, which could lead to misidentification in medical records.
Fujifilm Medical SystemsApr 30, 2021 - Lower riskMedical device
RanD S.r.l. recalls Hang&Go (kit for hyperthermic perfusion), Reference Code R9900120
RanD recalls Hang&Go kits (Reference Code R9900120) with specific lot numbers due to possible non-sterile products. Affected users should check their lot numbers and contact RanD for guidance.
RanDApr 30, 2021 - Lower riskMedical device
CooperSurgical, Inc. recalls CooperSurgical Wallach Loop Electrode 10mm x 10mm Square P/N: 909131. Disposable Universal Electrodes, LOOP electrodes,
CooperSurgical recalls 10mm x 10mm Square Wallach Loop Electrodes (P/N 909131) that were incorrectly packaged with round electrodes. This packaging error may lead to incorrect use during medical procedures.
CooperSurgicalApr 30, 2021 - Lower riskMedical device
Medline Industries Inc recalls Medline Tissue Recovery Instrument Set, Reorder #DYNJ64347A, packaged 3/case, Sterile, Rx. Convenience kit used to
Medline recalls sterile tissue recovery kits that may not meet minimum sterility requirements for medical use. Affected kits have specific lot numbers and packaging details.
MedlineApr 30, 2021 - Use cautionMedical device
Nico Corp. recalls Myriad-LX Light Source-for delivery of light to the surgical field to enhance visualization of tissue during resection
Nico Corp. recalls Myriad-LX Light Sources with serial numbers 350-00194D to 350-00475D due to potential tissue damage from sleeve occlusion during surgery. Updated instructions prevent light output reduction and sleeve blockage.
Nico Corp.Apr 30, 2021 - Lower riskFood
Indianapolis Fruit Company, Inc. recalls Garden Cut Coleslaw W/ Carrot Organic, 1lb plastic clamshell, UPC 053495081016, 4 1lb retail units per wholesale case.
Indianapolis Fruit Company recalls Garden Cut Coleslaw with carrot organic due to foreign plastic in product. Consumers should check UPC 053495081016 for affected items.
Indianapolis Fruit CompanyApr 30, 2021 - Lower riskFood
Nutralliance Inc recalls Medium Chain Triglyceride (MCT) Powder 50% from Coconut / CocoTrim packaged in 20 kilogram brown bags with plastic
Nutralliance recalls MCT powder 50% from coconut (CocoTrim) due to milk allergen contamination. Affected lots sold in 20kg brown bags. Consumers should check lot numbers and contact for details.
NutrallianceApr 30, 2021 - Lower riskMedical device
Medtronic Perfusion Systems recalls Medtronic HY10L28R3, Custom Pack HY10L28R3 1/4 Pack, Custom Perfusion System, Sterile, Rx.
Medtronic recalls specific lots of Custom Perfusion Systems due to potential insufficient welds that could cause leaks. Affected units have GTIN 00763000156879 and lot number 221679870.
Medtronic Perfusion SystemsApr 29, 2021 - Lower riskMedical device
Covidien, LP recalls Adult-Pediatric Electrostatic Filter HME, Item Code 352/5877Z - Product Usage: indicated for single use on anesthetized
Covidien recalls adult-pediatric electrostatic filter HME (item code 352/5877Z) due to potential deviations in ethylene oxide sterilization processes. This product is used for single-use anesthesia and respiratory care. Affected units have specific lot numbers and were sold with certain GTINs.
CovidienApr 29, 2021 - Stop using nowMedical device
Exact Medical Manufacturing, Inc. recalls Hays Ultrasound kit Item ID: H1000SE
Exact Medical recalls Hays Ultrasound kit H1000SE (lot 2005E090, 2006E495) due to lack of FDA 510(k) clearance for medical use. Consumers should not use this device for body openings.
Exact MedicalApr 29, 2021 - Lower riskDrug
Lupin Pharmaceuticals Inc. recalls Cefixime for Oral Suspension USP 100 mg/5mL, 50mL HDPE bottles, Rx Only, Manufactured by: Lupin Pharmaceuticals, Inc.
Lupin Pharmaceuticals recalls Cefixime oral suspension 100mg/5mL bottles due to subpotent drug content. This means the medication may not be as effective as labeled. Consumers should contact the manufacturer for details.
Lupin PharmaceuticalsApr 29, 2021 - UnratedDrug
Ascend Laboratories LLC recalls Olmesartan Medoxomil Tablets, USP, 20 mg, Rx Only, 30 Tablets, Manufactured by Alkem Laboratories Ltd, Mumbai, 400 013.
Ascend Laboratories recalls 20 mg Olmesartan Medoxomil tablets (NDC 67877-446-30) manufactured in India with foreign tablet risk. Stop using if you have the product.
Ascend LaboratoriesApr 29, 2021 - Lower riskDrug
Acella Pharmaceuticals, LLC recalls NP Thyroid 120 Thyroid Tablets, USP 2 grain (120 mg), packaged in a) 100-count bottles (NDC 42192-328-01) and b)
Acella Pharmaceuticals recalls NP Thyroid 120 tablets (120 mg) due to subpotent drug content. These tablets may not provide the intended thyroid hormone levels. Affected lots expired by August 2021.
Acella PharmaceuticalsApr 29, 2021 - Lower riskFood
Russ Davis Wholesale Inc recalls Veggie Pizza sold under the following brands: Crazy Fresh, quick & easy, and blank label. Item # 81068, Net Wt. 6.2
Russ Davis Wholesale Inc recalls Veggie Pizza products with undeclared soy lecithin. Check labels for brands Crazy Fresh, quick & easy, or blank label. Item # 81068, 6.2 oz. Keep refrigerated until use by date.
Russ Davis Wholesale IncApr 29, 2021 - Lower riskFood
Pepsico Inc recalls Evolve Vanilla Bean Plant-Based Protein Shake, 11oz "Tetra Pak" carton, sold 4 cartons per retail unit. UPC on retail 4
Pepsico recalls Evolve Vanilla Bean Plant-Based Protein Shakes with undeclared soy. Consumers should check UPC 876063007870 for affected units. No remedy specified in recall notice.
PepsicoApr 29, 2021 - Stop using nowConsumer product

Off-Road Motorcycles Recalled by American Honda Due to Crash and Injury Hazards (Recall Alert)
Honda recalls 2021 CRF450R off-road motorcycles due to potential drive chain breakage causing sudden loss of drive force and crash risks. Affected units have specific VIN ranges and red color.
HondaApr 29, 2021 - Use cautionConsumer product

Modernist Pantry Recalls Sodium Hydroxide Products Due to Failure to Meet Child Resistant Packaging Requirement and Violation of FHSA Labeling (Recall Alert)
Modernist Pantry recalls Kitchen Alchemy Sodium Hydroxide products due to unsafe packaging that could harm children. Products lack child-resistant packaging and required poison labeling, posing burn risks.
Modernist PantryApr 29, 2021 - Use cautionVehicle
HYUNDAI SANTA FE SPORT (2015) recall — Service Brakes, Hydraulic
Hyundai recalls 2015 Santa Fe Sport vehicles with potential engine compartment fire risk due to brake system electrical short. Owners must park away from structures until repair.
HyundaiApr 28, 2021 - Use cautionVehicle
BLUE BIRD ALL AMERICAN (2019) recall — Steering
Blue Bird is recalling certain 2018-2021 All American school buses due to potential loss of power steering causing crash risk. Owners should contact customer service for free replacement of the harness.
Blue BirdApr 28, 2021 - Use cautionVehicle
HYUNDAI ELANTRA (2021) recall — Seats
Hyundai recalls 2021 Elantra vehicles with improperly welded seat backs that could separate in a crash, increasing injury risk. Owners must have seats inspected or replaced free by dealers.
HyundaiApr 28, 2021 - Use cautionVehicle
BMW 330E (2021) recall — Seat Belts
BMW is recalling 2021 330e vehicles with improperly installed seat belt assemblies that may not restrain occupants, increasing injury risk. Owners will receive free repairs by dealers.
BMWApr 28, 2021 - Use cautionVehicle
HYUNDAI KONA (2020) recall — Engine
Hyundai is recalling certain 2020 Kona vehicles with a damaged engine that may stall or cause fire due to oil leaks. Owners must have their engine inspected by a dealer.
HyundaiApr 28, 2021 - Lower riskMedical device
Medtronic Vascular, Inc. recalls Endurant II/IIs Stent Graft System: STENT GRAFT ETBF3216C145E ENDUR II BIF. For treatment of vascular aneurysms.
Medtronic recalls Endurant II stent grafts with incorrect stentstop assembly (18fr) that could cause device malfunction during vascular aneurysm treatment.
MedtronicApr 28, 2021 - Lower riskMedical device
Randox Laboratories Ltd. recalls Randox RX Imola Analyser with ISE, Catalog Numbers RX4900, RX4900R
Randox recalls RX Imola Analyser with ISE models RX4900/RX4900R due to software freezing during command processing, resulting in no test results. Affected units have specific serial numbers and catalog codes.
RandoxApr 28, 2021 - Lower riskMedical device
Fresenius Medical Care Holdings, Inc. recalls Citrasate Liquid Acid Concentrate and NaturaLyte Liquid Acid Concentrate are each intended to be used as one component
Fresenius Medical Care recalls Citrasate and NaturaLyte Liquid Acid Concentrates due to potential freezing from refrigerated truck malfunctions. These products are used in hemodialysis. Affected lots have specific UDI numbers.
Fresenius Medical CareApr 28, 2021 - Lower riskDrug
Preferred Pharmaceuticals, Inc. recalls Preferred Pharmaceuticals Inc., Metformin HCl, Extended Release Tab. USP 500 mg, Generic for Glucophage XR, Rx Only,
Preferred Pharmaceuticals recalls Metformin XR tablets due to NDMA impurity exceeding safe limits. This may pose health risks with long-term use. Affected lots include C2520W through G2720A.
Preferred PharmaceuticalsApr 28, 2021 - Lower riskDrug
Fresenius Medical Care Holdings, Inc. recalls Sodium Chloride 0.9%, USP, 1000 mL, Mfg by: Fresenius Medical Care North America, Waltham, MA 02451, NDC 46163-0300-10
Fresenius Medical Care recalls 1000mL Sodium Chloride 0.9% due to temperature abuse risk. Product may be exposed to unsafe temperatures, causing potential issues. Check NDC 46163-0300-10 and lot numbers for affected units.
Fresenius Medical CareApr 28, 2021 - Use cautionFood
Croissant Etc Corp recalls 6" Round Croissant Crust 100 Count Bulk, frozen, Net Weight: 6.25 lbs. Croissant Etc. Corp., Greendale, WI 53129
Croissant Etc Corp recalls frozen 6-inch round croissant crusts because they contain undeclared soy lecithin, posing a risk to those with soy allergies.
Croissant EtcApr 28, 2021 - Lower riskFood
NOW Health Group Inc. recalls NOW 4x6 Acidophilus, 60 capsules per retail bottle. Item number 2920. UPC 7 33739 02920 1
NOW Health recalls 60-capsule Acidophilus bottles with foreign capsules and undeclared ingredients. Consumers should check product details and contact NOW for guidance.
NOW HealthApr 28, 2021 - Use cautionConsumer product

UST Recalls Bottles of LifeSeasons Blood Nourish-R Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning
LifeSeasons recalls Blood Nourish-R iron supplements due to non-child-resistant packaging. Risk of poisoning if young children access contents. Consumers should store out of reach and return for refund.
LifeSeasonsApr 28, 2021
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