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Latest recalls
34,894 found- Stop using nowConsumer product
Norco Bicycles Recalls Children's Bicycles Due to Fall Hazard
Norco recalls 2015-2017 children's bicycles with Samox SAC30-111NA cranks due to risk of bending or breaking, causing falls. Affected models include Storm 2.1, Charger 2.1, Fluid HT 2.3, and others. Consumers must stop using and get free crankset installation.
NorcoNov 7, 2017 - Lower riskMedical device
Southmedic, Inc. recalls Southmedic Sterile Disposable Scalpel Rx only Scalpels are intended to be used in various medical procedures for
Southmedic recalls sterile disposable scalpels due to non-sterile products in some lots. This could lead to infection during medical procedures. Affected lots include 092517.
SouthmedicNov 6, 2017 - Use cautionMedical device
Boston Scientific Corporation recalls Innova Self-Expanding Stent System, 200 mm. Labeled with Material Number and description as follows: Product Usage: The
Boston Scientific recalls Innova Self-Expanding Stent Systems (200mm) with material numbers H74939293052030 to H74939293082070 due to possible failure to fully release from delivery system.
Boston ScientificNov 6, 2017 - Lower riskMedical device
CareFusion 303, Inc. recalls Alaris Extension Sets with microbore tubing Model 20022 and 30914 Is used to administer fluid and medications from a
CareFusion recalls Alaris Extension Sets (Models 20022 and 30914) due to incorrect priming volume from manufacturing defects. Affected units include specific lot numbers. Consumers should contact CareFusion for details.
CareFusionNov 6, 2017 - Lower riskMedical device
Beckman Coulter Inc. recalls Access 2 Immunoassay System, Catalog Number 81600N. In vitro diagnostic device used for the quantitative,
Beckman Coulter recalls Access 2 Immunoassay System (Catalog 81600N) due to potential minor skin burns from reagent contact during pipettor alignment. Affected units have specific serial numbers.
Beckman CoulterNov 6, 2017 - Lower riskMedical device
Owen Mumford USA, Inc. recalls Unifine Pentips 5mm x 31G pen needles, packaged in 100 ct pen needles. Product Usage: Sterile, non-toxic,
Owen Mumford recalls 100-count packs of Unifine Pentips 5mm x 31G pen needles due to potential water exposure causing discoloration and sterility compromise. Affected units have specific UPC and batch numbers.
Owen MumfordNov 6, 2017 - UnratedDrug
Claris Lifesciences Inc recalls Ciprofloxacin in Dextrose (5%) Injection, USP 200 mg in 100 mL 5% Dextrose, Rx Only, (2 mg/mL), 100 mL Flexible Bag,
Claris recalls Ciprofloxacin in 5% Dextrose injection due to superpotent risk. This medication is for prescription use only and may cause serious harm if misused.
ClarisNov 6, 2017 - Use cautionDrug
West-Ward Pharmaceuticals Corp. recalls Dexamethasone Sodium Phosphate Injection, USP, 4 mg/mL, 1 mL Vials (NDC 0641-6145-01), packaged in 25 x 1 mL Vials per
West-Ward Pharmaceuticals recalls specific lots of Dexamethasone Sodium Phosphate Injection due to failed impurity specifications. Check your vials immediately.
West-WardNov 6, 2017 - Lower riskFood
Pacific Rim Distribution Inc. recalls Bean Boy Coffee Dark Chocolate Covered Espresso Beans
Pacific Rim Distribution Inc. recalls Bean Boy Coffee Dark Chocolate Covered Espresso Beans due to undeclared milk allergen. Check UPC 045635427075 for affected products.
Bean Boy CoffeeNov 6, 2017 - Use cautionVehicle
VOLKSWAGEN PASSAT (2014) recall — Engine And Engine Cooling
Volkswagen recalls 2012-2014 Passats with diesel engines for potential engine grease leaks that could cause fire if contacting hot surfaces like exhaust systems.
VolkswagenNov 5, 2017 - Use cautionVehicle
TOYOTA SEQUOIA (2017) recall — Wheels
Southeast Toyota is recalling 2017 Sequoia vehicles with specific 20-inch Rockstar wheels that may have cracked lugnuts causing wheel detachment. Owners should contact SET for free replacement.
Southeast ToyotaNov 5, 2017 - Use cautionVehicle
FREIGHTLINER CASCADIA (2017) recall — Power Train
Daimler Trucks North America recalls 2017 Freightliner Cascadia trucks with NFD tandem rear axles. Output shafts may fracture while descending grades, causing loss of compression braking and crash risk. Owners must contact DTNA for free output shaft replacement.
Daimler Trucks North AmericaNov 5, 2017 - Use cautionVehicle
THOMAS BUILT BUSES MINOTOUR (2018) recall — Seats
Daimler Trucks North America recalls 2016-2018 Thomas Built Buses Minotour school buses with seats lacking reinforcement brackets that could loosen in crashes, risking injury.
Thomas Built BusesNov 5, 2017 - Lower riskMedical device
Volcano Corporation recalls Volcano Imaging System s5i REF 807400001; CORE Mobile Imaging System (120V) REF 400-0100.01; CORE Mobile Imaging System
Volcano Corporation 121020083482
Volcano CorporationNov 3, 2017 - Use cautionMedical device
Handicare Usa Inc recalls Handicare C Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
Handicare recalls C Series patient lifts (models 323100-323917) due to risk of strap breakage when lifting patients over 625 lbs.
HandicareNov 3, 2017 - Lower riskMedical device
Medtronic Inc. recalls Everflex Self-Expanding Peripheral Stent with Entrust Delivery System Intended to improve luminal diameter in the
Medtronic recalls Everflex Self-Expanding Peripheral Stents with Entrust Delivery System due to potential label length mismatch. Affected models include EVD35-07-060-120 and EVD35-07-120-120. Contact Medtronic for details.
MedtronicNov 3, 2017 - Use cautionMedical device
Brainlab AG recalls BRAINLAB EXACTRAC VERO, Model/Catalog Numbers: 46228 EXACTRAC VERO 3.5 46238 EXACTRAC VERO 3.5 46216 EXACTRAC VERO SW
Brainlab recalls ExacTrac Vero 3.5 models due to potential treatment position errors. Affected units may not move to planned positions, risking inaccurate radiation therapy. Contact Brainlab for updates.
BrainlabNov 3, 2017 - Use cautionMedical device
Beaver-Visitec International Inc. recalls bvi Beaver EdgeAhead Safety Knife, (a) Sideport MVR .90mm 20G, REF 370531 (b) Sideport Angled, .60mm (23G), REF 378233
Beaver-Visitec recalls specific safety knives due to protective shield retracting, exposing the blade. Affected models include Sideport MVR .90mm 20G (REF 370531) and Sideport Angled .60mm (23G) (REF 378233).
Beaver-VisitecNov 3, 2017 - Lower riskMedical device
Beckman Coulter Inc. recalls UniCel DxH800, Part Numbers: 629029 and B24802, automated hematology analyzer
Beckman Coulter recalls UniCel DxH800 hematology analyzers with specific part numbers due to potential sample aspiration issues from shield interference. Affected units include models 629029 and B24802 with listed serial numbers.
Beckman CoulterNov 3, 2017 - Lower riskMedical device
Madison Polymeric Engineering recalls First Step Flexible Endoscope Bedside Pre-Clean Kit, EP-4. Intended for pre-clean of outer surface of flexible scopes
Madison Polymeric Engineering recalls EP-4 Flexible Endoscope Pre-Clean Kits due to potential microbial contamination exceeding safety limits. Affected lots may not meet required hygiene standards for medical use.
Madison Polymeric EngineeringNov 3, 2017 - Lower riskMedical device
Alden Optical recalls NovaKone Toric Daily Wear Soft contact; Catalog Number: AONKT54 Product Usage: The NOVAKONE TORIC lens is indicated for
Alden Optical recalls NovaKone Toric Daily Wear Soft contact lenses (Catalog AONKT54) due to lack of sterility assurance. Consumers should check if they have the specific model numbers listed.
Alden OpticalNov 3, 2017 - Lower riskMedical device
Stryker Neurovascular recalls Stroke Fast Pack(TM), Trevo(TM) XP, TREVO(TM) XP PROVUE RETRIEVER, 4 mm, 20 mm, ; Trevo(TM) Pro 18, TREVO PRO 18
Stryker recalls some Stroke Fast Packs and Trevo Procedure Packs due to mismatched carton labels and actual contents. Affected units may have incorrect contents, but no injury reports. Consumers should check labels and contact Stryker for details.
StrykerNov 3, 2017 - UnratedDrug
Mylan Pharmaceuticals Inc. recalls bupPROPion HCL Extended-Release Tablets, USP (XL) 300 mg, 500-count bottle, Rx only, Mylan Pharmaceuticals Inc.
Mylan Pharmaceuticals is recalling specific lots of 300 mg extended-release bupropion tablets due to failed impurity specifications from stability testing.
MylanNov 3, 2017 - Lower riskDrug
Ridge Properties, LLC recalls Extra Strength Naturally HL Liquid Hemorrhoid Relief Gel, (lidocaine HCL 4%), 1/2 oz Liquid Gel (NDC 69804-024-13), 1
Naturally HL recalls extra strength hemorrhoid relief gel due to inadequate manufacturing controls. All batches produced by Pain Relief Naturally are affected. Consumers should contact the company for details.
Naturally HLNov 3, 2017 - Lower riskFood
Gourmet Nut, Inc. recalls GourmetNut DARK CHOCOLATE COVERED ALMONDS NET WT 7oz (198g); UPC: 708747152203
Gourmet Nut recalls dark chocolate covered almonds with undeclared milk. Consumers should check UPC 708747152203 and lot dates for affected items.
Gourmet NutNov 3, 2017 - Use cautionConsumer product
JW Crawford Recalls Children's Rain Ponchos Due to Strangulation Hazard
JW Crawford recalls children's rain ponchos with a drawstring that can cause strangulation if entangled on playground equipment. Consumers should remove the drawstring or return for refund.
JW CrawfordNov 3, 2017 - Lower riskMeat & poultry
CC Kitchens LLC Recalls Meat and Poultry Products Produced Without Benefit of Inspection
USDA FSIS recalls 269 pounds of meat and poultry made without federal inspection, produced Nov 1, 2017. Consumers should contact CC Kitchens for details.
CC KitchensNov 2, 2017 - Lower riskMedical device
PerkinElmer Life and Analytical Sciences, Wallac, OY recalls NeoBase Succinylacetone Assay Solution, Product Number: 3042-0020; Affected UDI Numbers:
PerkinElmer recalls NeoBase Succinylacetone Assay Solution (Product #3042-0020) due to potential leaking vials that may cause minor allergic skin reactions if proper protective clothing isn't used. Affected lots identified by UDI numbers.
PerkinElmerNov 2, 2017 - Lower riskMedical device
Remel Inc recalls CM0405 Mueller-Hinton Broth IVD, 500g makes 23.8 litres.
Remel recalls Mueller-Hinton Broth IVD (500g) due to potential incorrect cation labeling, which could lead to inaccurate lab test results. Affected lots: 1865331, expiring 06/2021.
RemelNov 2, 2017 - UnratedMedical device
Pro-Med Instruments Gmbh recalls pmi, pro med instruments, DORO(R) Sterile Disposable Skull Pins, 3 pieces (3 pieces per blister, 12 blisters per box),
Pro-Med Instruments recalls sterile disposable skull pins due to reported pin tip breakage during surgery. Affected lots 17041 and 17272. No remedy specified in official notice.
Pro-Med InstrumentsNov 2, 2017
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