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
35,006 found- Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls DCA Vantage Handheld Barcode Scanner - Zebra Model - Model # DS4308 - HC0015BZZWW external accessory to DCA Vantage
Siemens Healthcare recalls DCA Vantage handheld barcode scanners with specific model numbers due to potential barcode data errors when configured for Code 39 with check digit.
Siemens HealthcareJun 30, 2020 - Use cautionMedical device
Medline Industries Inc recalls ClearPro Trach T-Piece Closed Suction Catheter, Model DYNCPTP14T, 14 Fr 12.5 IN FOR TRACHEOSTOMY TUBE - Product Usage:
Medline recalls ClearPro Trach T-Piece Closed Suction Catheter Model DYNCPTP14T due to reports of the catheter coming apart during use, which could cause injury. Affected patients should contact Medline for details.
MedlineJun 30, 2020 - Use cautionMedical device
CareFusion 303, Inc. recalls Alaris Pump Module Model 8100
CareFusion recalls Alaris Pump Module Model 8100 with all serial numbers due to broken elements that may cause inaccurate fluid delivery, over or under infusion risks.
CareFusionJun 30, 2020 - Use cautionMedical device
Hill-Rom, Inc. recalls Progressa Bed, Catalog No. P7500 - Product Usage: intended to be used to treat or prevent pulmonary or other
Hill-Rom recalls Progressa Bed model P7500 (serials V133AW9885-V142AW0261) manufactured May 2020 due to potential screw failure causing serious injury during medical use.
Hill-RomJun 30, 2020 - Lower riskMedical device
CareFusion 303, Inc. recalls Alaris Syringe Module Model 8110 - Product Usage: is intended to provide trained healthcare caregivers a way to
CareFusion recalls Alaris Syringe Module Model 8110 for potential dim LED display that could lead to inaccurate infusion monitoring. Affected units have specific serial numbers.
CareFusionJun 30, 2020 - Use cautionMedical device
CareFusion 303, Inc. recalls Alaris System PC Unit Model 8015. modular infusion pump and monitoring system
CareFusion recalls Alaris System PC Unit Model 8015 due to loose screws causing battery power loss and potential interruption of patient therapy. All units with serial numbers are affected.
CareFusionJun 30, 2020 - Use cautionMedical device
CareFusion 303, Inc. recalls Alaris System PC Unit Model 8015, a modular infusion pump and monitoring system
CareFusion recalls Alaris System PC Unit Model 8015 due to cleaning agents potentially damaging connectors, causing infusion interruptions. Affected units require specific cleaning steps to prevent therapy interruptions.
CareFusionJun 30, 2020 - Lower riskMedical device
Baxter Healthcare Corporation recalls Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8)
Baxter recalls SIGMA Spectrum Infusion Pump (Version 8) for updated cleaning instructions to prevent safety issues. No immediate action needed but follow new guidelines.
BaxterJun 30, 2020 - Lower riskMedical device
TELEFLEX MEDICAL INC recalls Pleur-Evac Adult-Ped Wet, LF Eng/Spanish, product code: A-8000I-06 - Product Usage: CHEST DRAINAGE: To evacuate air
Teleflex Medical recalls Pleur-Evac Adult-Ped Wet chest drainage systems due to potential sterile packaging compromise. Affected units have specific lot numbers. Consumers should check their product details.
Teleflex MedicalJun 30, 2020 - UnratedFood
Sundial Herbal Products recalls "SUNDIAL***Traditional Herbal Products***TRADITIONAL ORGANIC HERBS***WHITE JOINTA***1 oz.***USES: NERVES, COLD, ASTHMA,
Sundial Herbal Products recalls traditional organic herbs sold from 2014-2020 due to misbranding and unapproved drug claims. Products labeled for nerve, cold, asthma, and other uses are affected.
SundialJun 30, 2020 - Lower riskMedical device
Smith & Nephew, Inc. recalls PERI-LOC TARGETER 4.5MM DISTAL FEMUR, HANDLE, LEFT, NON-STERILE - Product Usage: used for adult and pediatric patients,
Smith & Nephew recalls PeriLoc Targeter 4.5mm Distal Femur handles marked as left but intended for right hand use. This could lead to incorrect surgical application. Affected units have specific product numbers and lot numbers.
Smith & NephewJun 29, 2020 - Lower riskDrug
RemedyRepack Inc. recalls Carbamazepine 200 mg Tablets, 100-unit dose tablets per box, Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA
RemedyRePack recalls 200mg Carbamazepine tablets with failed dissolution testing. This may affect medication effectiveness. Contact for return instructions.
RemedyRePackJun 29, 2020 - Lower riskDrug
EMD Serono, Inc. recalls Cetrotide (cetrorelix acetate for Injection) 0.25 mg, Sterile - for subcutaneous use only, Rx Only, Manufactured for:
EMD Serono recalls Cetrotide 0.25mg injections due to missing rubber stoppers that could compromise sterility. Affected lots from 2020 with specific NDC and expiration dates.
EMD SeronoJun 29, 2020 - Stop using nowDrug
Transliquid Technologies, LLC recalls Mystic Shield PROTECTION, ALCOHOL ANTISEPTIC 70%, Topical Solution, Antiseptic Hand Rub, Non-sterile Solution, Extra
Transliquid recalls Mystic Shield 70% alcohol antiseptic hand rub due to undeclared methanol contamination. Affected products have green or blue labels and were sold with UPC 787790339526. Consumers should stop using immediately.
TransliquidJun 29, 2020 - Stop using nowFood
Garland Ventures, LTD DBA Bally Plus recalls Freshness Guaranteed Five Cheese Stuffed Shells Traditional Italian Ricotta Filled Shells with Marinara Sauce 10.76
Bally Plus recalls 10.76oz Five Cheese Stuffed Shells with Listeria monocytogenes potential contamination. Affected lots F080SS and F090SS. Consumers should check UPC and discard if recalled.
Bally PlusJun 29, 2020 - Lower riskFood
Vitamin Shoppe recalls The Vitamin Shoppe Calcium Citrate Plus Magnesium & Vitamin D. 100 count (VS-1086; UPC:6653601086), 300 count (VS-1087;
Vitamin Shoppe recalls calcium citrate plus magnesium and vitamin d supplements due to sub-potent vitamin d levels. Affected products include 100-count (VS-1086) and 300-count (VS-1087) bottles.
Vitamin ShoppeJun 29, 2020 - Use cautionMeat & poultry
Pilgrim's Pride Corporation Recalls Chicken Breast Nugget Products due to Possible Foreign Matter Contamination
Pilgrim's Pride recalls 59,800 lbs of chicken breast nuggets from May 2020 due to possible rubber contamination. Consumers urged not to eat and dispose of products.
Pilgrim's PrideJun 28, 2020 - Use cautionVehicle
FOREST RIVER CHEROKEE WOLF PACK (2021) recall — Equipment
Forest River recalls 2021 Cherokee Wolf Pack toyhaulers with propane line near sharp edges that could leak, risking fire. Owners must have propane line rerouted or replaced free by July 17, 2020.
Forest RiverJun 26, 2020 - Use cautionVehicle
FOREST RIVER ROCKWOOD (2020) recall — Equipment
Forest River is recalling 2020-2021 Rockwood RLT2205S-W trailers due to an incorrect Federal Placard that could lead to overloading and loss of control. Owners should contact customer service for free replacement placards.
Forest RiverJun 26, 2020 - Lower riskMedical device
Steris Corporation recalls InnoWave Sonic Irrigator, There are currently six models (PCF, Pro, Ultra, Ultra+, Unity, and ECO) - Product Usage:
Steris recalls six models of InnoWave Sonic Irrigators due to unclear FDA test acceptance criteria during installation. Affected units have specific serial numbers. Consumers should check their serial numbers and contact Steris for details.
SterisJun 26, 2020 - Lower riskMedical device
Smiths Medical ASD Inc. recalls Medfusion Syringe Pump Model 4000; Software Versions V1.5.0, V1.5.1, V1.6.0, and V1.6.1
Smiths Medical recalls Medfusion Syringe Pump Model 4000 with specific software versions (V1.5.0-V1.6.1) due to potential inaccurate delivery of medication after interrupted bolus or loading doses. Affected units may require software update or replacement.
Smiths MedicalJun 26, 2020 - Lower riskMedical device
RANDOX LABORATORIES, LTD. recalls Randox Lipase Assay: Lipase Colorimetric R2 Substrate - Product Usage: A Lipase test system is a device intended for
Randox recalls specific Lipase Colorimetric R2 Substrate batches due to imprecision in patient sample testing. Affected units may yield inaccurate lipase test results.
RandoxJun 26, 2020 - Use cautionMedical device
Covidien Llc recalls Beacon EUS Access System Preloaded Access 135degree Needle sterile, single-use, endoscopic ultrasound device consisting
Covidien recalls Beacon EUS Access System Preloaded Access 135-degree needle for potential cannula detachment during procedures, risking delayed treatment, biliary leaks, or retained fragments.
CovidienJun 26, 2020 - Use cautionMedical device
Precision Valve & Automation,Inc recalls PVA, PREVENT is an FDA-authorized emergency ventilator designed to treat patients suffering from COVID-19 respiratory
FDA-authorized emergency ventilator for COVID-19 patients recalled due to rare false alarms and incomplete breathing cycles during operation. Affected units have specific serial numbers.
Precision Valve & AutomationJun 26, 2020 - Use cautionMedical device
Boss Instruments, Ltd. recalls BOSS DeBakey "Gator-Grip" Needle Holder 2 mm tip, 9", Part Numbers 50-2503 and 51-2503 - Product Usage: Endoscopic
Boss Instruments recalls specific endoscopic needle holders due to tungsten carbide plate breaking under pressure, potentially causing needle slippage during procedures.
Boss InstrumentsJun 26, 2020 - Use cautionVehicle
RAM PROMASTER (2020) recall — Air Bags
Chrysler recalls 2020 RAM Promaster vans and pickups with potentially detachable side curtain airbags that may not inflate properly in crashes, increasing injury risk. Owners must contact FCA US for free replacement.
ChryslerJun 25, 2020 - Lower riskMedical device
Philips North America, LLC recalls IntelliVue G7m Anesthesia Gas Module, Model no. 866173, Firmware Version 04.12.00, System Codes 453564477391,
Philips recalls IntelliVue G7m Anesthesia Gas Module with specific firmware version (04.12.00) due to potential gas measurement interruptions and alarms. Affected units have serial numbers listed in the recall notice.
PhilipsJun 25, 2020 - Lower riskDrug
POLARIZED LLC recalls Saniderm ADVANCED HAND SANITIZER, 70% Alcohol Content, 1 Liter bottles, Distributed by Polarized, LLC, Produced by
Polarized LLC recalls Sanider: 70% alcohol hand sanitizer bottles due to low ethanol content and undeclared methanol. Consumers should check lot numbers and contact for details.
POLARIZED LLCJun 25, 2020 - UnratedFood
HKH JVC LLC. recalls Garlic Shrimp Poke weighed and packed in plastic containers in the deli section per customer request. Cooked Shrimp is
HKH JVC LLC recalls Garlic Shrimp Poke sold in deli sections with potential Listeria monocytogenes contamination. Consumers should check best before dates and avoid consumption.
HKH JVCJun 25, 2020 - Lower riskFood
Chuckanut Bay Foods LLC recalls Red Velvet Layered Cheesecake is one whole cake (9" round cake) that has been pre-sliced into 14 slices and packaged in
Chuckanut Bay Foods recalls Red Velvet Layered Cheesecake due to undeclared walnut in the product. The mislabeled cake contains walnut pieces that could cause allergic reactions in sensitive individuals.
Chuckanut Bay FoodsJun 25, 2020
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