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
Orthofix U.S. LLC recalls Orthofix MINIRAIL, STANDARD LENGTHENER Model/Catalog Number: M101, Unilateral orthopedic/trauma external fixation device
Orthofix recalls MINIRAIL Standard Lengthener Model M101 due to mislabeling risks incorrect use. Check your device's model number against the recall list.
OrthofixJun 10, 2026 - Lower riskDrug
McKesson recalls Gemcitabine Injection, 1 g per 26.3 mL (38 mg/mL), 26.3 mL Single-Dose Vial, For Intravenous Infusion ONLY, Rx only,
McKesson recalls Gemcitabine injection vials stored at room temperature instead of refrigerated. This could affect cancer treatment safety. Check your NDC 0143-9341-01 lot CB0046 for affected units.
McKessonJun 10, 2026 - UnratedDrug
ACCORD BIOPHARMA INC recalls IMULDOSA, (ustekinumab-srlf) Injection, 130 mg/26 mL (5mg/mL), Rx only, Single dose vial, Manufactured by Accord
Accord BioPharma recalls IMULDOSA (ustekinumab-srlf) injections due to potential sterility issues. This medication is prescription-only and may be affected by specific lot numbers. Contact the manufacturer for details.
AccordJun 10, 2026 - Lower riskFood
Wells Enterprises, Inc. recalls Plastic 1-gallon clear pail blue label which reads in part as "BLUE RIBBON CLASSICS FRENCH VANILLA, MFD. BY WELLS
Wells Dairy recalls 1-gallon clear pails labeled 'BLUE RIBBON CLASSICS FRENCH VANILLA' due to elevated coliforms. Consumers should check product codes and contact Wells Dairy for details.
Wells DairyJun 10, 2026 - Stop using nowFood
Fry Pie Factory LLC recalls Pepperoni Rolls, Net Wt. 5 oz (141g), individually packaged in a clear plastic bag, UPC 601959803041
Fry Pie Factory LLC recalls 5 oz Pepperoni Rolls due to undeclared milk allergen and refrigeration issues. Check your UPC and sell-by dates.
Fry Pie FactoryJun 10, 2026 - Lower riskMedical device
Zimmer Surgical Inc recalls Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems Single Hose with CPC Connectors
Zimmer recalls A.T.S 4000 TS Tourniquet Systems Single Hose with CPC Connectors due to potential sterility breach in sealing area, which may cause moderate localized infection if used.
ZimmerJun 9, 2026 - Lower riskMedical device
CMR SURGICAL LIMITED recalls Brand Name: Versius Surgical System US Product Name: Vesius Surgeon Console US Model/Catalog Number: V-SS-1020 Software
CMR SURGICAL LIMITED recalls Vesius Surgeon Console software version 62.1 (model V-SS-1020) due to potential cybersecurity risks from missing Secure Boot. Affected units may need updates to prevent unauthorized access.
CMR SURGICAL LIMITEDJun 9, 2026 - Lower riskFood
GREENWORLD FOOD EXPRESS (USA) LLC recalls Al Yaman Halawa Extra Pistachio 907g (31.994 oz) plastic jars, UPC 5 287000 098083, 12 retail units per case
Greenworld Food Express recalls 12-unit cases of Al Yaman Halawa Extra Pistachio jars (UPC 5 287000 098083) due to possible Salmonella contamination. Consumers should check lot numbers and take action if affected.
Greenworld Food ExpressJun 9, 2026 - Lower riskPet food
Steve’s Real Food – Freeze Dried Chicken Recipe Cat and Dog Food: May contain low levels of thiamine (Vitamin B1)
Go Raw LLC recalls freeze-dried chicken cat and dog food due to potential low thiamine (vitamin B1) levels. Stop feeding affected products and return for refund or replacement.
Steve's Real FoodJun 8, 2026 - Lower riskMedical device
Hardy Diagnostics recalls HardyDisk AST Cefiderocol 30¿g (FDC30) REF Z9435 HardyDisk AST Cefiderocol 30¿g (FDC30) for in vitro agar diffusion
Hardy Diagnostics recalls HardyDisk AST Cefiderocol 30μg FDC30 (REF Z9435) for false susceptibility results in antibiotic testing, potentially causing ineffective treatment. Affected units may lead to delayed treatment or worsened infections.
Hardy DiagnosticsJun 8, 2026 - Lower riskMedical device
Stryker Corporation recalls STRYKER AHTO TUBE SET PACKAGING, Catalog Number 0250070600
Stryker recalls AHTO Tube Set Packaging (Catalog 0250070600) due to reported leaking from handpieces during use. Affected units include specific batch numbers.
StrykerJun 8, 2026 - UnratedMedical device
Windstone Medical Packaging, Inc. recalls AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) Laminectomy Pack, Pack Number AMS13574A; 2)
Windstone Medical Packaging recalls specific spine surgery kits for potential endotoxin level variations that could affect medical procedures.
Windstone Medical PackagingJun 8, 2026 - Lower riskMedical device
Micro Therapeutics, Inc. recalls Pipeline Flex Embolization Device with Shield Technology, 3.00 mm x 20 mm 027 REF PED2-300-20. Intracranial aneurysm
Micro Therapeutics recalls Pipeline Flex Embolization Devices with incorrect labeling that may cause improper use in intracranial aneurysm treatment.
Micro TherapeuticsJun 8, 2026 - Lower riskMedical device
Medline Industries, LP recalls Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons. KIT
Medline recalls convenience kits containing Bard Silastic Foley catheters (French sizes 16, 18, 20) due to increased surface material that may cause staining and potential harm.
MedlineJun 8, 2026 - Lower riskMedical device
Medline Industries, LP recalls MEDLINE medical procedure convenience kit labeled as: 1) TOTAL KNEE-LF, Medline kit SKU CDSOPT590T; 2) TOTAL KNEE-LF,
Medline recalls specific knee and hip procedure kits due to quality issues with pain management drugs that may not work as intended.
MedlineJun 8, 2026 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls ARTIS icono ceiling. Model Number: 11328100.
Siemens recalls ARTIS icono ceiling monitors (model 11328100) due to screws loosening over time, potentially causing the monitor to fall. Affected units may need repair or replacement.
SiemensJun 8, 2026 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Atellica CH Enzymatic Hemoglobin A1c (A1c_E). Material Number: 11097536.
Siemens recalls Atellica CH Enzymatic Hemoglobin A1c (A1c_E) devices due to potential for false low or high blood sugar results. Affected units may need recalibration or replacement.
Siemens HealthcareJun 8, 2026 - Lower riskMedical device
Klowen Braces recalls KL Owen Custom Orthodontic Solution, model/catalog number CIAS-800033,
Klowen Braces recalls KL Owen Custom Orthodontic Solution model CIAS-800033 due to potential incorrect bracket placement. Affected units include specific lot numbers and UDI/DI codes.
Klowen BracesJun 8, 2026 - Lower riskMedical device
ConvaTec, Inc recalls Aquacel Ag Surgical SP REF: 413556 9cm x 15cm/3.5 in. x 6 in., Sterile R
ConvaTec recalls Aquacel Ag Surgical SP dressings (lot 5G00809) manufactured with incorrect thickness. These dressings may not provide adequate wound coverage. Consumers should contact ConvaTec for details.
ConvaTecJun 8, 2026 - Lower riskDrug
ACCORD HEALTHCARE, INC. recalls Levothyroxine Sodium Tablets, USP, 300 mcg (0.3mg), 90 Tablets bottles, Rx only, Manufactured for: Accord Healthcare,
Accord Healthcare recalls 90-tablet Levothyroxine Sodium 300 mcg bottles due to subpotent drug content. This may not provide proper thyroid hormone levels. Consumers should contact pharmacy for guidance.
Accord HealthcareJun 8, 2026 - Lower riskDrug
Asclemed USA Inc. recalls Accucaine, Kit contains: Lidocaine HCl Injection USP, 1% (10 mg/mL), 5 mL single dose ampule, Rx Only, Distributed by
Asclemed recalls Accucaine 1% Lidocaine injection due to lack of sterility assurance. This may cause infections if used improperly. Contact the manufacturer for details.
AsclemedJun 8, 2026 - Use cautionDrug
ONESOURCE SPECIALTY PHARMA LIMITED recalls Methohexital Sodium for Injection, USP 500 mg Multiple Dose Vial, Rx Only, Manufactured by: OneSource Specialty, Pharma
OneSource Specialty Pharma recalls Methohexital Sodium 500mg vials due to impurities that could cause serious injury during medical use. Affected vials have specific lot numbers and expiration dates.
OneSource Specialty PharmaJun 7, 2026 - Stop using nowVehicle
YAMAHA XTZ690 (2025) recall — Exterior Lighting
Yamaha recalls 2025 XTZ690 motorcycles with turn signals that may fail to operate, increasing crash risk. Owners must stop riding until fixed; free replacement of meter assembly available.
YamahaJun 6, 2026 - UnratedFood
Wild Coast Brew LLC recalls The Lover Loose-Leaf Tea - Tart Chocolaty Tisane, net wt. 1.5oz (42 g). Product is packaged in cellophane bag within
Wild Coast Brew recalls 1.5oz Tart Chocolaty Tisane due to unsafe Ashw: risk of harm from consuming Ashwagandha root in tea blends.
Wild Coast BrewJun 5, 2026 - Stop using nowFood
Nelson & Isa Lacteos LLC recalls Requeson (soft ricotta) 1 lb. packed into a clear clamshell package with no labeling information. "Requeson" is
Nelson & Isa Lacteos recalls 1 lb. soft ricotta (Requeson) sold in unlabeled clamshell packages due to potential Listeria monocytogenes contamination. Consumers should avoid consumption.
Nelson & Isa LacteosJun 5, 2026 - UnratedMedical device
Medline Industries, LP recalls MEDLINE convenience kits labeled as: 1) TOTAL JOINT KIT, Medline Kit SKU DYKS1574A; 2) TOTAL KNEE BASIC, Medline Kit
Medline recalls specific convenience kits containing Bupivacaine Hydrochloride in Dextrose Injection due to quality issues from Huons Co, Ltd. Affected kits have unique SKUs and lot numbers listed in the recall notice.
MedlineJun 5, 2026 - Use cautionVehicle
HONDA CR-V HYBRID (2025) recall — Tires
Honda is recalling certain 2023-2026 CR-V Hybrid vehicles due to a tire repair kit cap that may detach, becoming a projectile. Owners should contact Honda for free replacement of the repair kit nozzle or sealant bottle.
HondaJun 5, 2026 - Lower riskMedical device
Philips North America Llc recalls Philips Telemetry Monitor 5500 1.4 GHz. Model Number: 867232. Includes the following system descriptions: TELE Monitor
Philips recalls Telemetry Monitor 5500 1.4 GHz (model 867232) due to potential reset to default state causing loss of configuration and failure to reconnect to central monitoring system.
PhilipsJun 5, 2026 - Lower riskMedical device
Integra LifeSciences Corp. (NeuroSciences) recalls OmniTract Surgical Retractor System, which includes 633 of the firm s product codes.
Integra LifeSciences recalls 633 OmniTract Surgical Retractor System models due to dry time not being extended to 90-120 minutes as required for sterilization cycles.
Integra LifeSciencesJun 5, 2026 - Lower riskMedical device
Medela Inc recalls Brand Name: Medela Product Name: ENFit ExSet Strl 60 2.0ml PV 1ct EN Model/Catalog Number: ENF060182LD / 101033086
Medela recalls ENFit ExSet Strl 60 2.0ml PV 1ct EN due to incompatible connectors that may cause delays in feeding or medication delivery. Affected units have model ENF060182LD or 101033086.
MedelaJun 5, 2026
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