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
35,021 found- Lower riskMedical device
CooperVision, Inc. recalls Brand Name: Pearle Vision 1 day Product Name: (somofilcon A) Contact Lens Model/Catalog Number: Pearle Vision 1 day
CooperVision recalls Pearle Vision 1 day contact lenses with incorrect power in some lots. Affected lenses may not provide proper vision correction. Consumers should check carton and blister lot numbers for affected items.
CooperVisionAug 12, 2026 - UnratedMedical device
INTERVASCULAR, SAS recalls Cardioroot Woven Collagen Coated Vascular Graft; Model Numbers: 1. HEWROOT0024, 2. HEWROOT0026, 3. HEWROOT0028, 4.
Intervascular recalls Cardioroot Woven Collagen Coated Vascular Grafts with model numbers HEWROOT0024-0034 due to failure in water permeability testing. Affected products may not meet quality standards.
IntervascularAug 12, 2026 - Lower riskMedical device
Straumann USA LLC recalls GM Helix Implant, REF: 109.984;
Straumann recalls GM Helix Implant REF: 109.984 due to packaging dimensions not matching the actual implant. Affected units may have incorrect size specifications.
StraumannAug 12, 2026 - Lower riskMedical device
Abiomed, Inc. recalls Impella Optical Controller, Automated Impella Controller, Impella Connect Package with the below product descriptions
Abiomed recalls Impella Optical Controller, Automated Impella Controller, and Impella Connect Package units with specific product codes and serial numbers due to potential purge cassette recognition issues from purge flag component failure.
AbiomedAug 12, 2026 - UnratedDrug
B BRAUN MEDICAL INC recalls Lactated Ringer's Injection USP, 1000 mL EXCEL container, Rx only, L7500, B. Braun Medical, Inc., Bethlehem, PA
B. Braun Medical recalls Lactated Ringer's Injection USP 1000mL (L7500) due to particulate matter. Affected units have specific lot numbers and expiration dates. Consumers should contact the manufacturer for details.
B. Braun MedicalAug 12, 2026 - Lower riskFood
Grand Central Bakery - Oregon Inc. dba Grand Central Bakery, Inc. recalls Product is Potato Sourdough Bread and sold under three following names: Potato Market Loaf 20oz. UPC 733163001576,
Grand Central Bakery recalls potato sourdough bread products due to potential metal pieces. Consumers should check labels for specific product names and UPCs to determine if affected.
Grand Central BakeryAug 12, 2026 - Stop using nowVehicle
BMW X3 (2025) recall — Steering
BMW recalls certain 2024-2026 X3 models due to an incorrectly attached steering spindle that may cause loss of control. Check your VIN for details.
BMWAug 12, 2026 - Lower riskMedical device
Shanghai United Imaging Healthcare Co., Ltd. recalls Computed Tomography X-ray System, Model: uCT 530 with software
Shanghai United Imaging Healthcare recalls CT X-ray system uCT 530 with software issue that prevents patient images from being visible on the Patient Administration interface, requiring rescans.
Shanghai United Imaging HealthcareAug 11, 2026 - Use cautionVehicle
THOMAS BUILT BUSES SAF-T-LINER C2 (2025) recall — Fuel System, Diesel
Daimler Trucks North America recalls 2024-2027 Thomas Built Buses Saf-T-Liner C2 transit buses due to potential fuel leaks during crashes that could cause fire. Owners received notification letters in September 2026.
Thomas Built BusesAug 11, 2026 - Use cautionVehicle
THOMAS BUILT BUSES SAF-T-LINER C2 (2025) recall — Fuel System, Diesel
Daimler Trucks North America recalls 2024-2027 Thomas Built Buses Saf-T-Liner C2 school buses due to incompatible fuel tank cage and fuel system that may cause fuel leaks and fire during crashes.
Thomas Built BusesAug 11, 2026 - Lower riskMedical device
Becton, Dickinson and Company recalls ForeSight Elite Tissue Oximetry Cable REF HEMFSM10 UDI-DI code: 00690103210927 The non-invasive ForeSight oximeter
Becton, Dickinson and Company - 10034992013, 10034992017, 10034992018, 10034992019
Becton, Dickinson and CompanyAug 11, 2026 - Use cautionMedical device
CooperSurgical, Inc. recalls INCA (Infant Nasal Cannulae Assy) Neonatal Nasal CPAP, Replacement Set. Stay-Flex tubing component. 5 units per box.
CooperSurgical recalls 4 model neonatal CPAP replacement sets with Stay-Flex tubing that may become loose, reducing CPAP pressure and oxygenation. Affected units have specific model numbers and lot codes.
CooperSurgicalAug 11, 2026 - Stop using nowMedical device
Medline Industries, LP recalls Medline Convenience Kits: 1) KIT ANESTHESIA L&D A- LINE SET, Catalog Number: DYKMBNDL199A
Medline recalls specific anesthesia L&D kits due to potential fungal contamination from Aspergillus penicillioides, which can cause serious infections or death. Affected kits have catalog numbers DYKMBNDL199A and specific lot numbers.
MedlineAug 11, 2026 - Stop using nowDrug
American Regent, Inc. recalls Epinephrine Injection, USP, 30 mg/30 mL (1mg/mL), 30 mL-Multiple-Dose Vial, Rx Only, For Intravenous Infusion,
American Regent recalls epinephrine injections with particulate matter and lack of sterility. Affected lots expire August 2026 through July 2027. Stop using immediately if you have these vials.
American RegentAug 11, 2026 - Lower riskMedical device
Baxter Healthcare Corporation recalls Baxter Novum IQ Syringe Pump, Loaner, Model Number 40800BAXUSL
Baxter recalls Novum IQ Syringe Pump model 40800BAXUSL due to software issue that may cause infusion errors when syringes are replaced during multi-syringe infusions. Affected units have specific serial numbers.
BaxterAug 11, 2026 - Stop using nowFood
CUISINE, KETTLE recalls Marketside Tomato Bisque Soup Kit, Tomato Bisque with Cheese Croutons & White Cheddar Cheese, Ready to Heat, Net Wt. 14
Marketside Tomato Bisque Soup Kit recalled due to presumptive positive Listeria monocytogenes test. Keep refrigerated until use by 8/22/2026.
CUISINE, KETTLEAug 11, 2026 - Lower riskFood
Byron White Formulas, Inc. recalls Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White
Byron White Formulas A-FNG Herbal Supplements (1.0 fl. oz.) may contain nuts but label does not declare walnuts in English. Consumers should check lot codes for affected products.
Byron WhiteAug 11, 2026 - UnratedMedical device
AVID Medical, Inc. recalls ROBOTIC PROSTATECTOMY PACK; Model/Item Number (Kit): NAMC423-11;
AVID Medical recalls 6 units of Robotic Prostatectomy Pack (Model NAMC423-11) due to potential lubricant contamination during manufacturing. Affected units were distributed nationwide in AZ, CA, FL, MD, NE, TX.
AVID MedicalAug 10, 2026 - Use cautionMedical device
American Contract Systems Inc recalls Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary Catheter Trays ABDOMINAL
American Contract Systems recalls 1,804 medical convenience kits containing BD CliniClean Pericare Wipes that may be contaminated with manufacturing lubricant, increasing risk of skin irritation or infection.
American Contract SystemsAug 10, 2026 - Use cautionMedical device
Merit Medical Systems, Inc. recalls Embosphere 500-700 micrometer 2 mL Syringe Sterile Steam, REF: S420GH/EUA, S620GH/EUA; Embosphere 700-900 micrometer 2
Merit Medical Systems recalls 104 units of Embosphere 500-700 micrometer syringes with packaging holes that could lead to infection if used. Stop using immediately.
Merit Medical SystemsAug 10, 2026 - Use cautionVehicle
BLUE BIRD VISION TRANSIT BUS (2025) recall — Electrical System
Blue Bird is recalling certain 2023-2027 Vision Transit Buses due to a damaged 12V power wire that may short circuit, increasing crash risk.
Blue BirdAug 10, 2026 - Lower riskMedical device
Cardinal Health 200, LLC recalls Presource Convenience Kits: 1) KIT, PRE OP , Catalog Number: AMN548616A; 2) KIT, NICU ADMIT NEW HAN , Catalog Number:
Cardinal Health recalls 14 types of Presource Convenience Kits due to potential open seals on applicators that could lead to skin infections or systemic infections if used improperly.
Cardinal HealthAug 10, 2026 - Lower riskMedical device
Medline Industries, LP recalls Medline Convenience Kits: 1) ANTERIOR SPINE PACK, Catalog Number: DYNJT10197; 2) CRANIOTOMY #IMF 56646-LF, Catalog
Medline recalls 109 convenience kits for potential elevated endotoxin levels in neurological sponges, which could cause medical issues like fever, inflammation, or low blood pressure. Affected kits have specific catalog numbers and lot numbers.
MedlineAug 10, 2026 - Lower riskMedical device
Medline Industries, LP recalls Medline convenience kits containing Healthmark Instrument Channel Brushes. SINUS PACK DYNJ48258D and Sinus Pack
Medline recalls specific sinus packs containing Healthmark Instrument Channel Brushes with potential sharp edges that could cause cuts or infection. Affected units include SINUS PACK DYNJ48258D and DYNJ48258F models.
MedlineAug 10, 2026 - UnratedMedical device
Bard Access Systems, Inc. recalls DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625150; DuoGlide Short-Term Straight Dialysis Catheter, REF:
Bard Access Systems recalls specific DuoGlide short-term dialysis catheters due to a downstream class I recall. Affected models include straight and curved extensions with reference numbers 5625150-5626240. This recall addresses safety concerns from a prior class I recall.
BardAug 10, 2026 - Lower riskMedical device
AVID Medical, Inc. recalls Haylard BASIC BIOPSY TRAY; Model/Item Number (Kit): PM415;
AVID Medical recalls Haylard Basic Biopsy Trays with model PM415 due to potential sterility issues with sodium chloride ampules. Affected kits may not be safe for medical use.
AVID MedicalAug 10, 2026 - Use cautionFood
Africando Foods LLC recalls Clear glass bottle with black screw lid with multi label which reads in part as "***AFRICANDO FOODS, LLC ALFREDO HOT
Africando Foods LLC is recalling Alfredo Hot Sauce because wheat and soybean oil are not listed on the label. Check your bottle for allergen info.
Africando FoodsAug 10, 2026 - Use cautionMedical device
Fresenius Medical Care Renal Therapies Group, LLC recalls 5008X Standard HD Pre-Flush Standard Blood Tubing Set Part Number 03-5110-6
Fresenius Medical Care recalls 5008X Standard HD Pre-Flush Standard Blood Tubing Set (Part 03-5110-6) due to heightened risk of blood leaks during dialysis treatment, potentially causing blood loss and hypovolemia.
Fresenius Medical CareAug 10, 2026 - Stop using nowVehicle
BLUE BIRD VISION SCHOOL BUS (2026) recall — Electrical System
Blue Bird recalls Vision School Buses due to a damaged 12V power wire that can short circuit, potentially causing loss of rear lighting or warning lights.
Blue BirdAug 10, 2026 - Stop using nowDrug
Fresenius Kabi USA, LLC recalls Tyenne (tocilizumab-aazg) Injection, 400 mg/20 mL (20 mg/mL), 20 mL vial, Rx Only, Manufactured by Fresenius Kabi USA,
Fresenius Kabi recalls Tyenne (tocilizumab-aazg) injection due to glass particles found in some batches. This may cause serious injury if injected. Affected units have specific lot numbers and expiration dates.
Fresenius KabiAug 10, 2026
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83,609 recalls tracked · 72,041 explained in plain English · 10,977 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.