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
35,004 found- Lower riskMedical device
Angiodynamics, Inc. recalls AngioDynamics NanoKnife Disposable Single Electrode Probes, Irreversible Electroporation (IRE) Device, 15 cm IRE Single
Angiodynamics recalls 15 cm IRE Single Electrode Probes due to RFID programming issue preventing recognition by the generator. Affected units may not function properly during medical procedures.
AngiodynamicsApr 24, 2020 - Lower riskMedical device
Physio-Control, Inc. recalls Infant Child Starter Kits, Part Number: 3202784-009, containing Infant/Child Reduced Energy Defibrillation Electrodes,
Physio-Control recalls Infant Child Starter Kits (part 3202784-009) with improperly sealed packaging for infant/child defibrillation electrodes, which could lead to contamination. Affected kits were sold from August 2017 to October 2019.
Physio-ControlApr 24, 2020 - Lower riskMedical device
Medtronic Sofamor Danek USA Inc recalls Medtronic Bone Void Filler, Small - Product Usage: is an injectable, moldable and biocompatible calcium phosphate bone
Medtronic recalls small bone void filler that may not set correctly, leading to longer surgery and potential bone healing issues. Affected units have specific product numbers and lot numbers.
MedtronicApr 24, 2020 - Lower riskMedical device
DeRoyal Industries Inc recalls DeRoyal Sterile Custom Kits packaged as a Piggy Back with the BD PosiFlush SF Saline Flush Syringe, labeled as follows:
DeRoyal recalls sterile custom kits with BD PosiFlush syringes due to packaging defects. Affected kits include specific model numbers and lot dates. Consumers should check their kits for the listed serial numbers and contact DeRoyal for details.
DeRoyalApr 24, 2020 - Lower riskMedical device
LivaNova USA Inc. recalls Sterile Disposable Connectors ASY 1/2 CONN W/LL STRLE 24 REF/ GTIN for Insert Label:050608000/ 00803622123382
LivaNova recalls sterile disposable connectors with specific lot numbers due to potential barrier breaches in packaging. Affected units may have compromised sterility during use.
LivaNovaApr 24, 2020 - Lower riskDrug
The Harvard Drug Group recalls Memantine Hydrochloride Extended-Release Capsules, 28 mg, 100 capsules per unit dose cartons, Rx only, Manufactured by:
Harvard Drug Group recalls 28mg Memantine Hydrochloride Extended-Release Capsules due to failed dissolution testing in stability checks. This affects Rx-only products with specific NDC and lot numbers.
The Harvard Drug GroupApr 24, 2020 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Esomeprazole Magnesium Delayed Release Capsules USP, 40 mg*, 1000-count bottles, Rx only, Mfd. By: Dr. Reddy's
Dr. Reddy's recalls 40mg esomeprazole capsules with brown pellets. No immediate risk but discoloration may indicate quality issues.
Dr. Reddy'sApr 24, 2020 - Use cautionVehicle
MCLAREN 720S (2019) recall — Fuel System, Gasoline
McLaren recalls 2016-2020 720S, Senna, GT, and 570GT models due to potential fuel leaks from corroded tanks causing fire risk. Free repairs to fix fuel tank corrosion.
McLarenApr 23, 2020 - Use cautionMedical device
Philips North America, LLC recalls ProxiDiagnost N90, UDI 706100
Philips recalls ProxiDiagnost N90 units with serial numbers starting with SN180000 or 100000. Incorrectly installed thermo switches may cause overheating and smoke if the device fails.
PhilipsApr 23, 2020 - Lower riskMedical device
Olympus Corporation of the Americas recalls OLYMPUS ShockPulse-SE Lithotripsy System, Model SPL-T Transducer
Olympus recalls specific ShockPulse-SE Lithotripsy System transducers with non-conforming materials that could allow water ingress during autoclaving. Affected units include serial numbers and lot numbers listed in the recall notice.
OlympusApr 23, 2020 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls ARTIS icono systems with Quantification Application SW (QVA/QCA) on a standalone XWP computer, an interventional
Siemens recalls ARTIS icono systems with Quantification Application SW (QVA/QCA) on standalone XWP computers. Using these may cause incorrect vessel detection and diagnosis, leading to inappropriate patient treatment.
SiemensApr 23, 2020 - Lower riskMedical device
Access Scientific LLC recalls BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 5Fr 8cm Max Barrier Kit. REF/UDI / 94116/10859821006237
Access Scientific recalls BD PosiFlush SF Saline Flush Syringe 10mL used in POWERWAND XL kits due to packaging holes compromising sterility. Affected units have REF/UDI 94116/10859821006237. No remedy specified in official notice.
Access ScientificApr 23, 2020 - Use cautionDrug
QuVa Pharma, Inc. recalls R.E.C.K. (Ropivacaine, Epinephrine, Clonidine, Ketorolac) in Sodium Chloride solution 50 mL in 60 mL Syringe,
QuVa Pharma recalls R.E.C.K. (Ropivacaine, Epinephrine, Clonidine, Ketorolac) vials with particulate matter risk. Affected lots and expiration dates listed.
QuVaApr 23, 2020 - Use cautionConsumer product
Naturo Sciences Recalls Eiji Essentials Wintergreen Oil Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
Naturo Sciences recalls Wintergreen Essential Oil due to non-child-resistant packaging, posing poisoning risk if young children swallow. Consumers should store out of reach and contact for refund.
Naturo SciencesApr 23, 2020 - Use cautionConsumer product
Natural Health Partners Recalls Dr. Mercola Wintergreen Essential Oils Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
Natural Health Partners recalls Dr. Mercola Wintergreen Essential Oils due to non-child-resistant packaging, risking poisoning if young children swallow. Consumers should store out of reach and contact for free replacement caps or refunds.
Natural Health PartnersApr 23, 2020 - Stop using nowConsumer product
LUS Recalls Hair Dryers Due to Electrocution or Shock Hazard (Recall Alert)
LUS recalls hair dryers with model HD-LUS01 that can electrocute if submerged in water while plugged in. Consumers should stop using and unplug immediately for refund or $175 credit.
LUSApr 23, 2020 - Stop using nowConsumer product
Leviton Manufacturing Recalls Electrical Connection Devices Due to Shock Hazard
Leviton recalls 50-ampere non-NEMA electrical connectors due to mislabeled terminals causing electrical shock. Consumers must stop using and return for free replacement.
LevitonApr 23, 2020 - Use cautionConsumer product
BioFinest Recalls Wintergreen Essential Oil Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning; Sold Exclusively at Biofinest.com (Recall Alert)
BioFinest recalls wintergreen essential oil due to non-child-resistant packaging, risking poisoning for young children. Affected products sold only at Biofinest.com; consumers should store out of reach and contact for refunds.
BioFinestApr 23, 2020 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls ARTIS Pheno - Interventional Fluoroscopic X-Ray System Model: 10849000 - Product Usage: is a family of dedicated
Siemens recalls specific ARTIS Pheno interventional fluoroscopy systems due to potential C-arm movement failures affecting imaging procedures. Affected units have serial numbers starting with 164011.
SiemensApr 22, 2020 - Lower riskMedical device
LABORIE MEDICAL TECHNOLOGIES, CANADA ULC recalls Pump Tube Set for MMS Libra and Solar Systems - Product Usage: Intended for use during water perfusion urodynamic
Laborie Medical recalls pump tube sets for MMS Libra and Solar systems due to potential packaging seal damage in a specific lot. Affected units may have compromised seals that could lead to improper use during urodynamic procedures.
Laborie MedicalApr 22, 2020 - Use cautionMedical device
BIOSENSE WEBSTER recalls PENTARAY NAV HIGH-DENSITY MAPPING CATHETER ELECTRODE EA 22 Rx only STERILE EO - Product Usage: The Biosense Webster
Biosense Webster recalls PENTARAY NAV High-Density Mapping Catheter electrodes due to risk of entrapment in cardiac valves during electroanatomic mapping procedures. Affected units include specific product codes manufactured from 2016 onward.
Biosense WebsterApr 22, 2020 - UnratedMedical device
Smith & Nephew, Inc. recalls smith&nephew R3 THREE HOLE HA COATED HEMISPHERICAL STIKTITE COATED SHELL, manufactured in the following sizes: Size
Smith & Nephew recalls R3 acetabular shells with out-of-specification manufacturing due to a production error. Affected sizes and lots listed in the recall notice.
Smith & NephewApr 22, 2020 - Lower riskFood
Royal International Trading Inc. recalls TAINY BOCTOKA DRY FRUITS MIX COMPOT APPLE; Assorted dried fruits; NET WT 17.63 oz (500g) clear plastic package
Royal International Trading recalls dried fruit mix due to undeclared sulfites. Consumers should check for the clear plastic package with container code 4705932006197.
Royal International TradingApr 22, 2020 - Lower riskMedical device
Bio-Rad Laboratories, Inc. recalls BioPlex 2200 Syphilis Total & RPR Linked Immunoabsorption Assay, Treponema pallidum:UDI:03610520653012 - Product Usage:
Bio-Rad recalls BioPlex 2200 Syphilis Total & RPR kit due to potential increased RPR reactivity in specific lots. Affected kits may produce inaccurate results for syphilis testing.
Bio-RadApr 21, 2020 - Lower riskMedical device
Ion Beam Applications S.A. recalls Proteus 235 The Proton Therapy System - Proteus 235 (brand names: Proteus Plus and Proteus ONE) is a medical device
Ion Beam Applications recalls Proteus 235 proton therapy systems where user signatures longer than 10 characters prevent resuming aborted treatments. This medical device affects specific models manufactured between May and November 2019.
Ion Beam ApplicationsApr 21, 2020 - Lower riskMedical device
Philips North America, LLC recalls Philips HeartStart XL Monitor/Defibrillators Model number: M4735A - Product Usage: is for use in the hospital by
Philips recalls 100+ hospital defibrillators (model M4735A) that may not have received required software updates. These devices are for trained medical staff only. Affected units have specific serial numbers listed in the recall.
PhilipsApr 21, 2020 - Lower riskDrug
Sandoz, Inc recalls Infuvite PEDiatric Pharmacy, kit in 1 carton (40 mL fill in a 50 mL) vial 1 and (10 mL) in vial 2, Rx Only, Distributed
Sandoz recalls pediatric Infuvite vitamin kits due to sub-optimal vial crimping. This may cause leaks or contamination. Affected kits have NDC 54643-5647-0, lot JX907, expiring 02/2021.
SandozApr 21, 2020 - Use cautionVehicle
FORD TRANSIT (2020) recall — Seat Belts
Ford Transit 2020 models with Freedman Seating Company seats may not secure occupants properly in crashes. Recall started May 13, 2020. Owners should contact dealers for free retractor replacements.
Ford TransitApr 20, 2020 - UnratedMedical device
ROi CPS LLC recalls Regard. Item number: 830034. GS0348D- CVC Triple Lumen 20CM non Sulfa-Mercy.
ROi CPS recalls Regard CVC Triple Lumen 20CM non Sulfa-Mercy items with lot numbers 68336DRW. These items contain PosiFlush syringes from a previous BD recall. Consumers should check their lot numbers and contact ROi CPS for details.
ROi CPSApr 20, 2020 - Use cautionMedical device
Bovie Medical Corporation recalls Renuvion/ J-Plasma Precise Open Handpiece. Catalog numbers BVX-044-BPS, BVX-044-BPP, BVX-150-BPP, BVX-150-BPS,
Bovie Medical recalls Renuvion handpieces with specific catalog numbers due to potential shaft fractures during surgery. Affected models were sold from June 2016 onward. Contact for return instructions.
Bovie MedicalApr 20, 2020
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