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
Terex Utilities recalls Power Over Fiber Base Module
Terex Utilities recalls Power Over Fiber Base Modules with incorrect laser class labeling. Products may not be certified for safety, risking injury from improper laser exposure. Affected units include specific part numbers.
Terex UtilitiesMay 11, 2026 - Use cautionMedical device
Fresenius Medical Care Holdings, Inc. recalls 5008X Blood Tubing Set, 24 units per case. Includes the below model numbers and descriptions. 1. 5008X HD Pre-Flush
Fresenius Medical Care recalls 5008X Blood Tubing Sets with potential online port errors when connecting SafeLine to substitution fluid port. Affected units include specific model numbers and lots manufactured after February 26, 2026.
Fresenius Medical CareMay 11, 2026 - Lower riskMedical device
Zimmer, Inc. recalls Brand Name: Persona Revision Product Name: Persona Revision¿ Trabecular Metal¿ Femoral Distal Augment Model/Catalog
Zimmer recalls Persona Revision Femoral Distal Augment model 42-5572-066-10 due to posterior augment found in distal package. Affected patients should contact Zimmer for details.
ZimmerMay 11, 2026 - Lower riskMedical device
Boston Scientific Corporation recalls Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device
Boston Scientific recalls Intera 3000 Hepatic Artery Infusion Pump AP-0300H due to potential drug leakage from the pump through the catheter. Affected units have specific serial numbers and GTIN.
Boston ScientificMay 11, 2026 - Lower riskMedical device
In2bones USA, LLC recalls NeoSpan¿ SuperElastic Compression Staple w/Instruments Catalog Number and Product Name T50 SN010 NeoSpan¿ SuperElastic
In2bones USA recalls NeoSpan SuperElastic Compression Staples due to missing Magnetic Resonance Conditional symbol on packaging and labels. This could lead to unsafe MRI scans if used without proper labeling.
In2bonesMay 11, 2026 - Lower riskMedical device
Inspire Medical Systems Inc. recalls Brand Name: Inspire Medical Systems, Inc. Product Name: Inspire stimulation Lead Model/Catalog Number: 4063 Product
Inspire Medical Systems recalls Model 4063 stimulation leads with incorrect Use By Dates that may lead to unplanned surgery. Affected units have specific serial numbers and were sold in the US. Contact for remedy details.
Inspire Medical SystemsMay 11, 2026 - Lower riskDrug
Haleon US Holdings LLC recalls Gas-X, Simethicone 125 mg/ ANTIGAS, 120 SoftGels, Distributed by: Haleon, Warren, NJ 07059, UPC: 3 00674 35041 9.
Haleon recalls Gas-X Simethicone 125mg 120-count softgels for incomplete inactive ingredient labeling on carton. Consumers should check product details and contact Haleon for more information.
HaleonMay 11, 2026 - Lower riskFood
HH FRESH TRADING CORP recalls HH Fresh Trading Corp. (branded) ENOKI MUSHROOM; Premium Quality; Net WT/ Poids Net 150g(5.29oz) Distributed by HH
HH Fresh recalls 150g Enoki mushrooms tested positive for Listeria Monocytogenes. Consumers should check UPC 4711498860002 for affected products.
HH FreshMay 11, 2026 - Stop using nowMeat & poultry
FSIS Issues Public Health Alert for Headcheese Deli Meat Products That May Be Contaminated With Listeria
FSIS alerts consumers that Daisy Brand headcheese products with a March 26, 2026 use-by date may be contaminated with Listeria monocytogenes. Consumers are urged not to consume these products and should discard or return them to the place of purchase.
Daisy Brand Meat ProductsMay 9, 2026 - Use cautionVehicle
TESLA MODEL 3 (2019) recall — Exterior Lighting
Tesla is recalling certain 2017-2023 Model 3 vehicles with overly bright low beams that could reduce visibility and increase crash risk. Owners must have headlights replaced free by Tesla.
TeslaMay 8, 2026 - Use cautionMedical device
Instrumentation Laboratory recalls GEM Premier 5000 with IQM2 Model/Catalog Number: 00024019255 and GEM Premier 7000 with iQM3 Model/Catalog Number:
Instrumentation Laboratory recalls GEM Premier 5000 and 7000 blood analyzers with specific bar code reader wands that may assign patient results to the wrong ID. Affected units have model numbers starting with 00024019255 or 00000015279.
Instrumentation LaboratoryMay 8, 2026 - Use cautionMedical device
AMD Medicom Inc. recalls Ritmed Neurological Sponges, Description/REF: 0.5x0.5in, Non-Sterile/55992C; 0.5x1.0in, Non-Sterile/55993C; 0.5x3.0in,
AMD Medicom recalls Ritmed Neurological Sponges (0.5x0.5in to 1.0x3.0in) due to potential endotoxin levels that could cause neurovascular issues during surgery. Affected lots distributed after May 2022.
AMD MedicomMay 8, 2026 - Use cautionMedical device
Think Surgical, Inc. recalls TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia Tracking Array REF 109004 UDI-DI code:
Think Surgical recalls TMINI Femur and Tibia Tracking Arrays with specific UDI-DI codes due to a knob that may loosen, causing potential misalignment during knee replacement surgery. Affected units must be checked for the codes listed.
Think SurgicalMay 8, 2026 - Lower riskMedical device
GE Medical Systems SCS recalls GE Healthcare AW Server 3.2 ext.6.5; Radiological Image Processing System
GE Healthcare recalls AW Server 3.2 ext.6.5 software due to potential patient image mix-ups causing misdiagnosis. Affected users should check product details and contact GE for updates.
GE Medical SystemsMay 8, 2026 - Lower riskMedical device
Datex-Ohmeda Inc recalls Giraffe Stand-alone Infant Resuscitation System; Powered emergency ventilator (resuscitator) Product identifiers:
Datex-Ohmeda Inc is a leading medical device manufacturer specializing in critical care monitoring systems, patient monitoring equipment, and advanced medical technology solutions.
Datex-OhmedaMay 8, 2026 - Lower riskMedical device
Merit Medical Systems, Inc. recalls Splashwire Hydrophilic Guide Wire: REF: MSWSTDA35150 UDI-DI codes: 00884450529645 00884450529669 00884450529690 REF:
Merit Medical recalls Splashwire Hydrophilic Guide Wire with unsealed pouches that may cause contamination during medical procedures. Affected units have specific UDI-DI codes and lot numbers. Consumers should contact Merit for details.
Merit MedicalMay 8, 2026 - Use cautionMedical device
Ventec Life Systems, Inc. recalls VOCSN+Pro package, REF: PRT-00853-000; VOCSN+Pro unit, REF: PRT-00490-001
Ventec Life Systems recalls VOCSN+Pro ventilators with potential backup alarm failure during power loss. Affected units may not alert caregivers if primary power fails, risking delayed response to hazardous conditions.
Ventec Life SystemsMay 8, 2026 - UnratedDrug
UCB Biosciences Inc. recalls cimzia (certolizumab pegol), 2x200mg/mL PREFILLED SYRINGES (2 single-dose), Rx ONLY, Manufactured by: UCB Inc., Smyrna,
UCB Biosciences recalls cimzia prefilled syringes due to lack of sterility assurance. These injectable medications may cause infections if used.
UCB BiosciencesMay 8, 2026 - Lower riskFood
Fly By Jing Inc. recalls Fly By Jing (branded) Creamy Sesame Noodles; 3.8 oz packets. Sold in single and 4 packs. Single UPC: 8-50052-23988-6 4
Fly By Jing recalls Creamy Sesame Noodles packets due to possible peanut cross-contamination. Consumers should check UPCs and lot codes for affected items.
Fly By JingMay 8, 2026 - Lower riskFood
J and J Bunting, Inc recalls Lunds & Byerly's Curry Powder Sweet
Lunds & Byerly's Curry Powder Sweet (Lot 0082026U00232) was mislabeled as sesame seeds white. Consumers should check labels for correct product name.
J and J BuntingMay 8, 2026 - Use cautionVehicle
RAM 2500 (2025) recall — Power Train
Chrysler recalls certain 2023-2026 RAM 2500 trucks due to a powertrain software error that may cause loss of vehicle control. Owners will receive free software updates from dealers.
ChryslerMay 7, 2026 - Lower riskMedical device
PIE Medical Imaging B.V. recalls 3mensio Workstation (Vascular Fenestrated) software
PIE Medical Imaging recalls specific versions of 3mensio Workstation software for vascular imaging due to potential overestimation of cardiovascular measurements by up to 34.4% in certain use cases.
PIE Medical ImagingMay 7, 2026 - Lower riskMedical device
AVID Medical, Inc. recalls Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.
AVID Medical recalls Halyard EYE PACK convenience kits with model LVEY27 due to incorrect Betadine solution concentration. Affected units have specific lot numbers and expiration dates.
AVID MedicalMay 7, 2026 - Use cautionVehicle
CADILLAC ESCALADE (2026) recall — Power Train
General Motors recalls 2026 Cadillac Escalade vehicles with potential front or rear wheel lockup during driving, increasing crash risk. Owners must stop driving until transfer case is replaced by dealers.
CadillacMay 7, 2026 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Siemens Dimension Tacrolimus Flex Reagent Cartridge (TAC), REF DF207, SMN 10700795; enzyme immunoassay
Siemens recalls Dimension Tacrolimus Flex reagent cartridges (lots FA6254, FA6260, FA6286) due to possible positive bias in quality control and patient test results. Affected units may show inaccurate results.
Siemens HealthcareMay 7, 2026 - Use cautionMedical device
Draeger, Inc. recalls Atlan A350XL. Model Number: 8621600. anesthesia workstation
Draeger recalls Atlan A350XL anesthesia workstations with model 8621600 due to potential piston ventilator failure before use or mechanical ventilation failure during use. Affected units have specific serial numbers listed in the recall notice.
DraegerMay 7, 2026 - UnratedMedical device
TELEFLEX LLC recalls Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb Neurosponge Strips
Recall of 1,481,700 US units of Pilling Wecksorb Neurosponges (cotton) due to potential endotoxin levels. Affected models include 200100-200131 with specific UDI codes and batch numbers. No remedy stated in official notice.
Pilling WecksorbMay 7, 2026 - Lower riskMedical device
Fresenius Medical Care Holdings, Inc. recalls Bicarby Dialysate; Model number: RFP-400-G;
Fresenius Medical Care recalls Bicarby Dialysate model RFP-400-G due to incorrect GTIN labeling that may lead to wrong potassium solution use. Affected units have specific lot codes.
Fresenius Medical CareMay 7, 2026 - Use cautionFood
Llorens Pharmaceuticals International Division, Inc. recalls Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement, Net Wt. 8 FL Oz (237mL) Amber PET modern round 24-400
Llorens Pharmaceuticals recalls vitamin supplements with black particles that could cause harm. Stop using affected bottles before expiration.
Llorens PharmaceuticalsMay 7, 2026 - Stop using nowConsumer product
ZMC Group Recalls Multiple Light Up Toys Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys
ZMC Group recalls multiple battery-operated light up toys because button cell batteries can cause serious injury or death if swallowed by children. Consumers must stop using, remove batteries, and submit proof of destruction for a refund.
ZMC GroupMay 7, 2026
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