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
34,959 found- Lower riskMedical device
Cook Inc. recalls Neff Percutaneous Access Set, Catalog Number NPAS-100-RH-NT
Cook recalls Neff Percutaneous Access Set (NPAS-10:00-RH-NT) due to potential missing bottom seal on packaging, risking unsterile use. Affected units sold with lot 8373482.
CookMay 2, 2019 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls EnCor Breast Biopsy Probes, packaged individually in sterile pouches, 5 pouches/carton, single use, Rx, catalog/REF
Bard recalls EnCor Breast Biopsy Probes with leaks and suction problems. Affected units have specific lot numbers. Stop using if you have these probes.
BardMay 2, 2019 - Lower riskMedical device
SenTec AG recalls SenTec Standard Starter Set with and without Service Gas (2 changers each) - Product Usage: Is indicated for
SenTec recalls standard starter sets for potential low electrolyte during membrane changes. This may affect CO2 and oxygen monitoring in medical devices. Affected lots listed in the recall notice.
SenTecMay 2, 2019 - Lower riskMedical device
Rinovum Women's Health recalls Revive Reusable Bladder Support, Model No. 0025 - Product Usage: The Revive bladder support is intended for temporary
Rinovum recalls Revive Reusable Bladder Support Model 0025 that may split or crack after 31 uses, risking leaks or injury. Owners should check product details and contact for remedy.
Rinov: Women's HealthMay 2, 2019 - Lower riskDrug
Septodont Inc. recalls Articaine DENTAL, Articane hydrochloride 4% and epinephrine 1:100,000, 50 cartridges. 1.7 mL each, Rx only,
Septodont recalls 50-cartridge dental products labeled incorrectly as Articadent Dental, causing confusion with Xylocaine Dental. Mislabeling may lead to incorrect medication use.
SeptodontMay 2, 2019 - Lower riskDrug
Unipharma, Llc. recalls DrKids Children's Pain & Fever Oral Solution Acetaminophen 160 mg/5 mL, 20 Pre-measured Single-Use Vials 0.17 fl. oz.
Unipharma recalls DrKids Children's Pain & Fever Oral Solution due to potential contamination with bacteria B. cepacia. Affected units include 20 vials with NDC 70302-011-20.
UnipharmaMay 2, 2019 - Stop using nowFood
Dole Fresh Vegetables recalls Dole Colourful Coleslaw ( Salade Chou Coloree) - Canada Shredded green and red cabbage and carrots. Net Wt. 3 lbs. 1.36
Dole Fresh Vegetables recalls Dole Colourful Coleslaw due to complaints of soft plastic pieces. Check lot B102011 and use-by date 05-02-19.
DoleMay 2, 2019 - Stop using nowFood
Life Rising Corporation recalls Life Rising Holder-W Holder Warmer capsules, 54 count bottle
Life Rising Corporation recalls 54-count Holder-W Warmer capsules purchased before May 2, 2019 due to high lead levels. Consumers should stop using these products immediately.
Life RisingMay 2, 2019 - Stop using nowConsumer product
Greenfield World Trade Recalls Food Dehydrators Due to Fire Hazard
Greenfield World Trade recalls Excalibur EZ DRY 5-tray food dehydrators with model TTEVM50W or EVM50W due to fire hazard from overheating. Consumers must stop using and get a refund.
Greenfield World TradeMay 2, 2019 - Stop using nowConsumer product
FIRMAN Power Equipment Recalls Portable Generators Due to Fire Hazard; Sold Exclusively at Costco (Recall Alert)
FIRMAN P03615 portable generators sold at Costco have a fire hazard due to carbon canister gas leaks. Return for refund or get free repair at FIRMAN service center.
FIRMANMay 2, 2019 - Stop using nowConsumer product
BRP Recalls Snowmobiles Due to Fuel Leak and Fire Hazard (Recall Alert)
BRP recalls 2017 Ski-Doo MXZ, Summit and Renegade snowmobiles with 850 E-TEC engines due to fuel leaks that could cause fire. Affected vehicles have specific colors and model numbers printed on the side panels.
BRPMay 2, 2019 - Use cautionMedical device
B. Braun Medical, Inc. recalls B.Braun Infusomat Space Volumetric Infusion Pump Administration Set, Catalog Number 363032
B. Braun recalls specific infusion pump sets that may leak or disconnect at the Y-site joint, causing potential injury. Affected units have catalog number 363:032 and lot number 0061641410.
B. BraunMay 1, 2019 - Use cautionMedical device
Abbott Vascular recalls Abbott MitraClip XTR Clip Delivery System, UDI: 08717648226366, Part: CDS0601-XTR, Sterile EO, Rx Only
Abbott recalls MitraClip XTR Clip Delivery System due to risk of clips opening unexpectedly during implantation, potentially requiring additional surgery. Affected units have specific serial numbers.
Abbott VascularMay 1, 2019 - Lower riskMedical device
Medtronic Navigation, Inc.-Littleton recalls Medtronic 0-arm TM 1000 Imaging Systems: Bl-700-00027-XXX and B1-700-00028-XXX (where XXX indicates the system
Medtronic recalls 0-arm TM 1000 Imaging Systems with serial numbers Bl-700-00027-XXX and B1-700-00028-XXX where XXX indicates system voltage. If the charger board is faulty, the system may not take X-rays or move properly, affecting surgery.
MedtronicMay 1, 2019 - Lower riskMedical device
Abbott Laboratories, Inc recalls ARCHITECT C System Mixer - Product Usage: The ARCHITECT Clinical Chemistry System is designed to perform automated
Abbott recalls ARCHITECT C System Mixer models LN 09D59-01, 02, 03 due to risk of mixer blade detaching, which can cause inadequate sample mixing in clinical chemistry tests.
AbbottMay 1, 2019 - UnratedDrug
Golden State Medical Supply Inc. recalls Losartan Potassium Tablets USP 25 mg 30 count bottle NDC 60429-316-30 Rx only GSMS Incorporated
FDA-confirmed impurity in Golden State Medical Supply's Losartan Potassium Tablets may exceed safe levels. Recalled due to CGMP deviations. Check NDC 60429-316-30 for affected products.
Golden State Medical SupplyMay 1, 2019 - Lower riskFood
U.S. Tov, Inc. recalls Dragonfly Dehydrate Guava Ing: Guava, Sugar, Salt Net Wt: 5.25 ozs 150g Distributed by: U.S. Trading Company Product of
U.S. Tov recalls Dragonfly Dehydrate Guava (5.25 oz) due to undeclared sulfites. Consumers should check lot numbers and contact the company for details.
U.S. TovMay 1, 2019 - UnratedFood
Maine Wild Blueberry Company recalls 30 Lbs IQF Wild Blueberries, Keep Frozen -10*C
Maine Wild Blueberry Company recalls 30 lbs IQF frozen blueberries from January 2019 after internal testing found Listeria Monocytogenes. Product was never distributed to consumers.
Maine Wild Blueberry CompanyMay 1, 2019 - Lower riskFood
Heritage Candy Company recalls First Street Dark Chocolate Nonpareils; 12 oz. stand up re-sealable plastic bags. Ingredients: Sweet Chocolate (sugar,
Heritage Candy Company recalls 12 oz. dark chocolate nonpareils bags due to potential almond contamination. Consumers should check for bags with dark chocolate almonds and contact the company for details.
Heritage Candy CompanyMay 1, 2019 - Use cautionConsumer product
Starbucks Recalls Bodum Recycled Coffee Presses Due to Laceration Hazard
Starbucks recalls Bodum + Starbucks recycled coffee presses due to laceration risk from broken plunger knobs. Consumers must stop using and return for store credit refund.
StarbucksMay 1, 2019 - Stop using nowConsumer product
DAVIDsTEA Recalls Valentine’s Day Stackable Mugs Due to Fire Hazard
DAVIDsTEA recalls Valentine's Day stackable mugs that are mislabeled as microwave safe, posing a fire hazard if microwaved due to metallic print. Consumers should stop using and return for refund.
DAVIDsTEAMay 1, 2019 - Stop using nowVehicle
SPARTAN GLADIATOR (2014) recall — Equipment
Spartan recalls 2004-2016 Gladiator vehicles due to tiller frame cracks that may cause the aerial device to fall. Free inspection and reinforcement available.
SpartanApr 30, 2019 - Use cautionVehicle
COACHMEN BEYOND (2020) recall — Equipment
Forest River is recalling 2019-2020 Coachmen Beyond motorhomes with ProAir AC systems due to undersized wiring that could overheat and cause fire. Owners must have wiring replaced free by dealers.
Forest RiverApr 30, 2019 - Lower riskMedical device
Stryker GmbH recalls Endotrac EPF/EGR Hook/Triangle Blade Kit, Catalogue Number 3056-1
Stryker recalls Endotrac EPF/EGR Hook/Triangle Blade Kit (Catalogue 3056-1) due to potential compromised sterile bag seals. Affected units include specific lot numbers. Consumers should contact Stryker for details.
StrykerApr 30, 2019 - Lower riskMedical device
Cardinal Health 200, LLC recalls Monoject Standard Hypodermic Needle, 20 G x 1-1/2" bulk Item code: 8881200664
Cardinal Health recalls 20G x 1.5" Monoject needles due to potential sterility compromise from manufacturing defects. Affected lots: 905657, 906327, 906341.
Cardinal HealthApr 30, 2019 - Lower riskMedical device
Beckman Coulter Inc. recalls Beckman Coulter ACCESS Immunoassay Systems, Access Total T3 Triiodothyronine , REF 33830 (UDI: 15099590227210) for use
Beckman Coulter recalls ACCESS Total T3 Triiodothyronine assays (REF 33830) due to potential biotin interference at high levels, causing inaccurate results. Affected units include specific models and lots.
Beckman CoulterApr 30, 2019 - UnratedDrug
Preferred Pharmaceuticals, Inc recalls Losartan Potassium Tab. USP 50mg, a) 30 count bottle (NDC 68788-0048-03) and b) 90 count bottle (NDC 68788-0048-09), Rx
Preferred Pharmaceuticals recalls 50mg Losartan Potassium tablets due to FDA-confirmed impurity NMBA above safe levels. Consumers should check NDC codes and contact the company for details.
Preferred PharmaceuticalsApr 30, 2019 - Use cautionDrug
Par Pharmaceutical, Inc. recalls Mycophenolate Mofetil for Injection, USP 500 mg, 4 Single Dose Vials, Rx Only, Distributed by: Par Pharmaceutical
Par Pharmaceutical recalls Mycophenolate Mofetil injection vials due to glass fragments found in one vial after reconstitution. Affected patients should contact their healthcare provider for guidance.
Par PharmaceuticalApr 30, 2019 - Stop using nowDrug
Direct Rx recalls Losartan Potassium 100 mg, 30 Tabs bottles, Rx only, Packaged and Distributed By: Direct Rx Dawsonville, GA 30534 NDC
FDA recalls Direct Rx Losartan Potassium 100mg tablets due to impurity NMBA above safe levels. Consumers with this specific product should stop using it.
Direct RxApr 30, 2019 - Lower riskDrug
Sagent Pharmaceuticals Inc recalls Ketorolac Tromethamine Injection, USP, 60 mg per 2 mL (30 mg per mL), 2 mL Vials, Rx only, Mfd. for Sagent
Sagent Pharmaceuticals recalls Ketorolac injection vials due to potential microbial growth during manufacturing. This could introduce harmful bacteria into the product. Affected vials have specific NDC and lot numbers.
Sagent PharmaceuticalsApr 30, 2019
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