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
34,894 found- UnratedDrug
Medisca, Inc. recalls Aminocaproic Acid, USP (6-Aminohexanoic Acid) active pharmaceutical ingredient, packaged in a) 100 g jar (NDC
Medisca recalls Aminocaproic Acid (USP) jars and drums that were manufactured for industrial use but labeled for pharmacy compounding. This may pose risks if used in medical settings without proper safety checks.
MediscaSep 14, 2017 - Lower riskFood
Country Harvest, Inc. recalls Country Harvest brand Lentil Barley Soup, dried soup mix is packaged in poly pro bag, heat sealed and placed in another
Country Harvest recalls Lentil Barley Soup due to missing milk declaration on label despite listing dairy whey. Check UPC 7 29818 00103 9 for affected products.
Country HarvestSep 14, 2017 - Lower riskFood
Shawnee Milling Company, Inc. recalls Shawnee Mills Peppered Gravy Mix, 2.75 oz and 24 oz.
Shawnee Mills recalls peppered gravy mix due to potential foreign material. Consumers should check product dates and contact for details.
Shawnee MillsSep 14, 2017 - Stop using nowConsumer product
Southwire Recalls Globe and Snow Globe Stake Lights Due to Fire Hazard
Southwire recalls Moonrays mystic globe and snow globe stake lights due to fire risk from light refraction. Stop using immediately and return for refund.
MoonraysSep 14, 2017 - Use cautionVehicle
HEARTLAND SUNDANCE XLT TT (2018) recall — Suspension
Heartland recalls 2018 Sundance XLT TT trailers with improper axle installation that may reduce braking ability or cause brakes to lock up. Owners should contact Heartland for free correction.
HeartlandSep 13, 2017 - Use cautionVehicle
CRUISER RV SHADOW CRUISER ULTRA LITE (2018) recall — Suspension
Cruiser recalls 2018 Shadow Cruiser Ultra Lite trailers with backward axle installation that may reduce braking ability or cause temporary brake lockup. Owners should contact customer service for free correction.
Cruiser RVSep 13, 2017 - Use cautionMedical device
Covidien LLC recalls Endo GIA Auto Suture Universal Articulating Loading Unit for use in abdominal, gynecologic, pediatric and thoracic
Covidien recalls Endo GIA Auto Suture Universal Articulating Loading Units due to potential safety interlock failure, which could allow firing an empty unit twice during surgery.
CovidienSep 13, 2017 - Lower riskMedical device
Medtronic Vascular, Inc. recalls Medtronic Aptus Heli-FX Thoracic EndoAnchor System Heli-FX Guide 42 mm, REF HG-18-90-42, STERILE EO, Rx Only The
Medtronic recalls specific Heli-FX Thoracic EndoAnchor System guides due to mismatched deflection length labels on packaging versus actual product. This may affect medical procedures requiring precise catheter handling.
MedtronicSep 13, 2017 - Lower riskMedical device
The Metrix Company recalls SECURE(R) 100mL EMPTY VINYL CONTAINER With 2 Ports - (5 Boxes of 40), REF 58719, STERILE R,
Metrix recalls 5-box sets of sterile 100mL vinyl containers with incorrect material labeling. The bags are actually PVC, not as labeled. No action needed.
MetrixSep 13, 2017 - Use cautionMedical device
Zimmer Biomet, Inc. recalls 14-442000S Antegrade Femoral Nail Instrument Kit, orthopedic instrument
Zimmer Biomet recalls 14-442000S Antegrade Femoral Nail Instrument Kit due to risk of bolt fracture during femoral nail insertion, potentially causing injury.
Zimmer BiometSep 13, 2017 - UnratedDrug
Amgen, Inc. recalls Procrit (epoetin alfa), 10,000 units/mL, packaged in a) box of 6 single use 1 mL vials (NDC 59676-310-01), b) box of 25
Amgen recalls Procrit (epoetin alfa) 10,000 units/mL vials due to glass flakes found during quality checks. Affected lots expire July 2018. No remedy specified in recall notice.
AmgenSep 13, 2017 - Lower riskDrug
Vi-Jon, Inc. recalls Equate Beauty Clarifying Face Daily Moisturizer 4 fl. oz. (118 mL) Distributed by: Wal-Mart Stores, Inc. Bentonville,
Equate Beauty Clarifying Face Daily Moisturizer 4 fl. oz. (118 mL) with failed stability specifications is recalled. This product may not remain stable and could cause skin irritation or other issues.
Equate BeautySep 13, 2017 - UnratedDrug
Vi-Jon, Inc. recalls Magnesium Citrate Oral Solution Cherry Flavor, 1.745 g per fl oz, packaged in 10 fl. oz ( 296 mL) bottles, Labeled as
Vi-Jon recalls cherry-flavored magnesium citrate oral solution bottles due to failed impurities and degradation specifications. Affected products include specific NDC/UPC codes sold at CVS, Meijer, and Life Brand stores.
Vi-JonSep 13, 2017 - Stop using nowConsumer product
Target Recalls Room Essentials 4-Drawer Dressers Due to Tip-Over and Entrapment Hazards
Target recalls Room Essentials 4-drawer dressers sold in black, espresso, and maple due to unstable construction that can tip over, causing serious injury or death to children.
Room EssentialsSep 13, 2017 - Lower riskMedical device
Abbott Point Of Care Inc. recalls i-STAT DE handheld data processing module for clinical use, Software Version 2.8, List Number:08K46-01115200 (UDI:
Abbott recalls i-STAT DE handheld data processing modules with software version 2.8. These units may not update patient lists or custom reference ranges, but do not cause erroneous results.
AbbottSep 12, 2017 - Lower riskMedical device
Toshiba American Medical Systems Inc recalls Toshiba Medical Kalare Fluoroscopic X-Ray System (DREX-KL80) Kalare is intended to be used as a universal diagnostic
Toshiba recalls DREX-KL80 X-ray system due to images not displaying on monitor or saving to hard disk during exams. Affected units may have imaging errors affecting patient care.
ToshibaSep 12, 2017 - Lower riskMedical device
Terumo Medical Corporation recalls Destination Guiding Sheath catheter introducer, Catalog Number: RSR06 Product Usage: The Destination¿ Guiding Sheath is
Terumo recalls Destination Guiding Sheath catheter introducers with catalog number RSR06 that may have tucking depth marginally outside specifications. This could affect medical procedures.
TerumoSep 12, 2017 - Use cautionMedical device
Otto Bock Healthcare Product recalls OTTO BOCK Kenevo knee joints Model 3C60=ST
Recall for Otto Bock Kenevo knee joints Model 3C60=ST where pylon may break after 2.3 years of heavy use, risking falls. Affected units sold in US/Canada with specific serial numbers.
Otto BockSep 12, 2017 - Use cautionMedical device
Zoll Manufacturing Corp. recalls LifeVest Wearable Defibrillator Model 4000, Product Number 10A0988-A01. The LifeVest system is indicated for patients
Zoll recalls LifeVest Model 4000 wearable defibrillators due to potential shock failure during self-checks. Affected units have specific serial numbers. Contact Zoll for details.
ZollSep 12, 2017 - Lower riskMedical device
St. Jude Medical, Inc. recalls Infinity 5 Implantable Pulse Generator and Infinity 7 Implantable Pulse Generator Models 6660, 6661, 6662, 6663
St. Jude Medical recalls Infinity 5 and 7 Implantable Pulse Generator models 6660-6663 with serial numbers implanted before September 12, 2017. The device may show incorrect battery life due to errors in the Clinician Programmer or Patient Controller.
St. Jude MedicalSep 12, 2017 - Lower riskFood
Vitamin Cottage Natural Food Markets, Inc. recalls Natural Grocers Organic Deglet Noor Dates, Target weight is 0.60 - 0.70 lb random weight package, Zip lock plastic bag.
Natural Grocers recalls organic deglet noor dates due to potential undeclared coconut. Consumers should check labels for lot code 198-17.
Natural GrocersSep 12, 2017 - Use cautionVehicle
HONDA CIVIC (2017) recall — Power Train
Honda recalls 2017 Civic sedans and coupes with potentially weak halfshafts that could cause vehicle roll away if parking brake isn't engaged. Affected owners should contact Honda for free repairs.
HondaSep 11, 2017 - Use cautionMedical device
Zimmer Biomet, Inc. recalls BlockAid Cut Resistant Surgical Glove Liners, combine stainless steel and synthetic fibers woven together to form a cut
Zimmer Biomet recalls cut-resistant surgical glove liners that lack sterility assurance. Affected items have specific item and lot numbers. Consumers should stop using these liners to prevent infection risks during medical procedures.
Zimmer BiometSep 11, 2017 - UnratedDrug
United Therapeutics Corp. recalls TYVASO (treprostinil) Inhalation Solution Treprostinil 1.74 mg/2.9 mL (0.6 mg/mL) Tyvaso Inhalation System Starter Kit
United Therapeutics recalls TYVASO inhalation solution (treprostinil) with CGMP deviations. Affected units include specific model and lot numbers. Consumers should contact the company for details.
United TherapeuticsSep 11, 2017 - Lower riskFood
Diversified Foods and Seasonings, Inc recalls Homestyle Broccoli and Cheese Soup, 1.66 lb Plastic boil-n-bag pouches, frozen, Contains: Milk, Soy, Wheat
Diversified Foods recalls frozen Homestyle Broccoli and Cheese Soup pouches after customer reports plastic pieces in the product. Consumers should check product details and contact the company for guidance.
Diversified FoodsSep 11, 2017 - Use cautionVehicle
HAUL MASTER UTILITY TRAILER (2017) recall — Tires
Harbor Freight is recalling 2014-2017 Haul Master Utility Trailers with tires that may fail under load, risking crashes. Owners get free tire replacements.
Harbor FreightSep 10, 2017 - Lower riskVehicle
THOR MOTOR COACH WINDSPORT (2018) recall — Equipment
Thor Motor Coach is recalling certain 2017-2018 Windsport motorhomes due to potentially incorrect water capacity labels that could lead to vehicle overload and increased crash risk. Owners should contact TMC for corrected labels.
Thor Motor CoachSep 10, 2017 - Use cautionVehicle
FOREST RIVER PUMA (2018) recall — Wheels
Forest River recalls 2018 Puma trailers with wheels that may loosen and detach while moving, causing crash risk. Owners must have wheel center caps replaced free by dealers.
Forest RiverSep 10, 2017 - Use cautionMedical device
Medtronic Inc. recalls Medtronic MiniMed(TM) Pro-set(TM) (MMT-280, 281)
Medtronic recalls MiniMed Pro-set (MMT-280, 281) due to potential insulin over-delivery. Affected units include specific lot numbers. Consumers should contact Medtronic for details.
MedtronicSep 10, 2017 - Use cautionMeat & poultry
Northside Noodle Company Recalls Meatball Products Due To Misbranding and Undeclared Allergens
USDA recalls Northside Noodle meatball mixes due to soy allergen not listed on labels. Consumers should discard or return products to avoid allergic reactions.
Northside NoodleSep 8, 2017
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