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
34,946 found- Stop using nowFood
Albertsons Inc recalls Signature Reserve Bourbon Maple Blondie Ice Cream 14 FL OZ UPC 2113009912
Albertsons Inc recalls Signature Reserve Bourbon Maple Blondie Ice Cream due to undeclared tree nuts. Check your UPC and best-by date.
Signature ReserveSep 26, 2018 - Stop using nowConsumer product
CFMOTO Recalls All-Terrain Vehicles Due to Fire Hazard
CFMOTO recalls 2016-2018 CFORCE ATVs with 400-500cc engines due to fuel hose cracking causing fire risk. Owners must stop using and get free repairs.
CFMOTOSep 26, 2018 - Stop using nowConsumer product
Boy Scouts of America Recalls Neckerchief Slides Due to Violation of Federal Lead Content Ban
Boy Scouts of America recalls neckerchief slides due to lead content. Stop using immediately and return for a free replacement.
Boy Scouts of AmericaSep 26, 2018 - Use cautionVehicle
VOLVO VNL (2019) recall — Engine And Engine Cooling
Volvo recalls 2016-2019 VNL trucks with Cummins ISX15 engines due to potential fuel line bursts causing leaks and engine stalling. Owners must replace filter banjo bolts by November 21, 2018.
VolvoSep 25, 2018 - Lower riskMedical device
Pro-Dex Inc recalls PRO-DEX Surgical Driver Battery Pack PDBP-001 Series PRO-DEX Battery Pack, Single Pouch - PDBP-001-2 PRO-DEX Battery
Pro-Dex recalls surgical battery packs with visual particulates in Tyvek pouches. These sterile batteries risk contamination during surgery. Affected units include PDBP-001-2 and PDB:040-2 models from specific lots.
Pro-DexSep 25, 2018 - Use cautionMedical device
GE Healthcare, LLC recalls Giraffe Incubator Carestation. Neonatal incubator. Device sold under the following product names: Carestation and
GE Healthcare recalls Giraffe Incubator Carestation neonatal incubators with potential electric leakage. Affected units have specific model numbers and serial codes. Stop using immediately if you own one.
GE HealthcareSep 25, 2018 - Lower riskMedical device
DT MedTech, LLC recalls DT Medi Tech Hintermann Series Talar Implant LEFT-SIZE 4 Part Number: 302114 components are prostheses for a mobile
DT MedTech recalls LEFT-SIZE 4 Talar Implant components (part 302114) due to incorrect labeling. Affected units may have wrong size identification.
DT MedTechSep 25, 2018 - Lower riskMedical device
Cook Medical Incorporated recalls Zilver 635 Biliary Stent 14mm x 30mm, Catalog Number: ZIB6-80-14.0-30 Product Usage: The Zilver 518 and 635 Biliary
Cook Medical recalls Zilver 635 Biliary Stent 14mm x 30mm (ZIB6-80-14.0-30) due to incorrect deployment instructions in the user manual. This correction prevents potential complications during stent placement.
Cook MedicalSep 25, 2018 - Lower riskDrug
Baxter Healthcare Corporation recalls Levofloxacin Injection in 5% Dextrose, 5 mg/mL, packaged in a) 50 mL (NDC 36000-046-24), b) 100 mL (NDC 36000-047-24),
Baxter Healthcare recalls specific levofloxacin injection products due to high drug concentration levels in solution. These products were manufactured with out-of-specification results for levofloxacin, potentially causing adverse effects. Affected patients should contact the manufacturer for guidance.
Baxter HealthcareSep 25, 2018 - Lower riskDrug
RXQ Compounding LLC recalls Lidocaine 1% + Epinephrine 1:100,000 (MDV) INJ SOL, 50 mL per glass vial, Rx only, 340 West State Street, Unit 9,
RXQ Compounding LLC recalls Lidocaine 1% + Epinephrine 1:100,000 injection solution due to subpotent drug testing. This affects specific vials with NDC 7073197450, lot 04042018:58, expiring 10/17/18.
RXQ Compounding LLCSep 25, 2018 - Lower riskDrug
Right Value Drug Stores, Inc. recalls Tadalafil SR 12 mg Capsules packed in 8,13, 20, 30, 40 or 60 dram screw top pill bottle, Carie Boyd's Prescription Shop
Right Value Drug Stores recalls Tadalafil SR 12mg capsules with specific bottle sizes and lots due to misbranding. Consumers should check labels for NDC 99999-9969-51 and affected lots.
Right Value Drug StoresSep 25, 2018 - Lower riskFood
Whole Foods Market recalls 365 Everyday Value Brand White Corn Chips, Salted NET WT 20 oz. (1 LB 4 OZ) 567 g packaged in a plastic bag
Whole Foods Market recalls 365 Everyday Value White Corn Chips due to possible undeclared milk content. Consumers should check packaging for Best By dates and UPC 9948247145.
Whole Foods MarketSep 25, 2018 - Stop using nowConsumer product
Traeger Grills Recalls Wood Pellet Grills Due to Fire Hazard
Traeger recalls Scout and Ranger portable wood pellet grills due to grease leaks from drip trays that can cause fires. Consumers must stop using and get a free replacement or refund.
TraegerSep 25, 2018 - Use cautionConsumer product
Provata Health Recalls Promotional Activity Trackers Due to Burn Hazard
Provata Health recalls promotional activity trackers that can overheat and cause burns. Consumers should stop using or charging the wristbands immediately and contact for free replacement.
Provata HealthSep 25, 2018 - Use cautionConsumer product
Desert Harvest Recalls Reléveum Skin Repair Cream Due to Failure to Meet Child Resistant Closure Requirements
Desert Harvest recalls Reléveum Skin Repair Cream due to non-child-resistant packaging. This poses poisoning risk if young children swallow the cream. Consumers should remove from reach of children and get free child-resistant cap replacement.
Desert HarvestSep 25, 2018 - Use cautionVehicle
GRAND DESIGN IMAGINE (2019) recall — Suspension
Grand Design is recalling 2019 Reflection, Imagine and Transcend travel trailers due to potential hub overheating and fire risk from missing inner bearings in axles.
Grand DesignSep 24, 2018 - Lower riskMedical device
Invivo Corporation recalls Xper Flex Cardio Physiomonitoring System, Software version 1.6.0.0388
Invivo recalls Xper Flex Cardio Physiomonitoring System software version 1.6.0.0388 due to potential freezing of invasive blood pressure readings during certain actions. Affected units have specific serial numbers listed in the recall notice.
InvivoSep 24, 2018 - Lower riskMedical device
PerkinElmer Health Sciences Canada, Inc. recalls PerkinElmer QSight 210 MD Mass Spectrometer Simplicity 3Q MD v1.0 with Hot Fix 2 Software intended to identify
PerkinElmer recalls QSight 210 MD mass spectrometers with Hot Fix 2 software that may overwrite last sample data when automatic flush is enabled. Affected units have specific part numbers.
PerkinElmerSep 24, 2018 - Lower riskMedical device
Johnson & Johnson Surgical Vision Inc recalls Disposable 25GA Vitrectomy Cutter, REF NGP0025, RX Only, Abbott Medical Optics Inc., The product provides the item
Johnson & Johnson Surgical Vision recalls disposable 25GA Vitrectomy Cutters (REF NGP0025) sold for surgery due to packaging error. A 20GA cutter may be in a 25GA package, risking surgical technique changes.
Johnson & Johnson Surgical VisionSep 24, 2018 - Lower riskMedical device
Roche Diagnostics Corporation recalls Roche Diagnostics URISYS 1100 Urine Analyzer Part Number: 03617556001 Product Usage: The URISYS 1100 Urine Analyzer is
Roche recalls URISYS 1100 urine analyzers with specific part numbers due to potential false negatives for protein, nitrite, leukocytes, and erythrocytes. Affected units may not detect these substances correctly.
RocheSep 24, 2018 - Lower riskMedical device
Becton Dickinson & Co. recalls BD Max Instrument, Catalog Number 441916 441927 (refurbished instrument) - Product Usage: The BD MAX System, used in
Becton Dickinson recalls BD Max instruments (catalog 441916-441927) due to false positive Candida glabrata results when Trichomonas vaginalis is present. Affected units have serial numbers CTI1201-CTI1288.
Becton DickinsonSep 24, 2018 - Lower riskFood
Lutosa S.A. recalls Lutosa Foodservice Quality Plain Mashed Produced in Belgium 2.5 kg/5.5 lb
Lutosa Foodservice Quality Plain Mashed potatoes from Belgium (2.5kg) with specific lot numbers may contain plastic and rubber pieces. Consumers should check lot numbers and contact Lutosa for details.
LutosaSep 24, 2018 - Lower riskFood
Harris Teeter recalls Harris Teeter Low Fat FROZEN YOGURT cookies & cream 1.5 QUART (1.42l) CONTAINS: MILK, WHEAT, SOY PROUDLY DISTRIBUTED
Harris Teeter recalls low-fat frozen yogurt cookies & cream due to peanuts not listed in ingredients. This could cause allergic reactions for those with peanut allergies.
Harris TeeterSep 24, 2018 - Use cautionMeat & poultry
Junior's Smokehouse Processing Plant Recalls Beef Jerky Products due to Possible Foreign Matter Contamination
Junior's Smokehouse is recalling beef jerky products that may contain pieces of hard metal. Consumers are urged not to consume these items and should discard or return them to the place of purchase.
Junior's SmokehouseSep 21, 2018 - Use cautionVehicle
SPARTAN METROSTAR (2017) recall — Exterior Lighting
Spartan is recalling 2017 MetroStar emergency vehicles with Whelen brake lights that may illuminate without braking, risking crashes. Owners will get free brake light repairs by October 2018.
SpartanSep 21, 2018 - Use cautionVehicle
KIA SORENTO (2018) recall — Steering
Kia recalls certain 2018 Sorento vehicles with improperly welded cowl crossbar that may cause steering column separation, increasing crash risk. Owners will receive free replacement.
KiaSep 21, 2018 - Use cautionVehicle
KENWORTH T680 (2019) recall — Engine And Engine Cooling
PACCAR recalls 2019 Kenworth T680 trucks with Cummins ISX15 engines due to potential fuel line bursts causing leaks and engine stalling. Owners must contact PACCAR for free fuel pump screen replacement.
PACCARSep 21, 2018 - Use cautionVehicle
HEARTLAND WILDERNESS (2019) recall — Suspension
Heartland is recalling 2019 travel trailers with missing hub bearing races that could cause hub separation and crash risk. Owners must contact Heartland for free hub or axle replacement.
HeartlandSep 21, 2018 - Use cautionMedical device
Encore Medical, Lp recalls Exprt Precision System: Revision Hip, Proximal Body with Bolt, Lateral Offset, Sterile R, djo surgical, REF:
Encore Medical recalls specific revision hip implants due to loose proximal body bolts that may cause pain or need for additional surgery. Affected models include 495-00-065 to 495-01-085.
Encore MedicalSep 21, 2018 - Lower riskMedical device
Becton Dickinson & Co. recalls BD FocalPoint Slide Profiler and BD FocalPoint GS Review Station; Catalog Nos. 490398, 490653, 491085, 491086, 491090,
BD recalls FocalPoint Slide Profiler and GS Review Station models with catalog numbers 490398, 490653, 491085, 491086, 491090, and others. The device may not function at temperatures below 15°C, but this issue does not cause harm to patients or users. Labeling has been updated to indicate a minimum operating temperature of 18°C.
Becton DickinsonSep 21, 2018
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