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Latest recalls
34,959 found- Stop using nowConsumer product
Bodum Recalls Stove Top Espresso Makers Due to Fire and Burn Hazards
Bodum recalls Chambord stove top espresso makers due to fire and burn hazards. Stop using immediately and return for a full refund.
BodumApr 23, 2019 - Lower riskMedical device
Luminex Corporation recalls Verigene Processor SP, Model Numbers: 10-0000-07 and 10-0000-07-R
Luminex recalls Verigene Processor SP models 10-0000-07 and 10-0000-07-R due to repeated No Call results. Affected units have specific serial numbers listed in the recall notice.
LuminexApr 22, 2019 - Lower riskMedical device
Cook Inc. recalls Cook Kwart Retro-Inject Ureteral Stent Set: PRODUCT/CATALOG NUMBER/GPN: 4.7 Fr 003500 G14916; 6.0 Fr 003600 G14836; 7.0
Cook recalls specific ureteral stent sets due to missing warning for stent knotting. Affected models include 4.7 Fr, 6.0 Fr, and 7.0 Fr sizes with certain lot codes. No action is required as the hazard is not severe enough to warrant immediate stop use.
CookApr 22, 2019 - UnratedDrug
RemedyRepack Inc. recalls Losartan Potassium/HCTZ, 100 mg/12.5 mg Tablet, 90-Count bottle, Manufactured by Torrent Pharmaceuticals, Distributed
FDA-confirmed impurity in Losartan Potassium/HCTZ tablets may exceed safe levels. Recalled batch: NDC 70518-1560-00, Lot B05170:101618, expiring 10/2019. Consumers should contact manufacturer for details.
RemedyRepackApr 22, 2019 - Lower riskDrug
Zydus Pharmaceuticals USA Inc recalls Carvedilol Tablets, USP, 3.125 mg, 500-count bottle, Rx Only, Manufactured by: Cadila Healthcare Ltd., India;
Zydus Pharmaceuticals recalls 3.125mg Carvedilol tablets due to foreign tablets found in some bottles. Customers should check their bottles for light yellow fragments.
Zydus PharmaceuticalsApr 22, 2019 - UnratedDrug
Inopak Ltd recalls Mild Health Care Antibacterial Hand Soap, .6% P.C.M.X., packaged in a) 1000 ml Disc Pump pouches, 8 x 1000 ml Disc Pump
Inopak recalls mild antibacterial hand soap with CGMP deviations. Products may not meet safety standards due to manufacturing issues. Consumers should check batch numbers and contact Inopak for details.
InopakApr 22, 2019 - Lower riskFood
Island Desserts Llc DBA Pastry Art recalls Key Lime and Cream Torte, 5 oz., Keep in Freezer for up to 6 months or refrigerated for 5 days
Island Desserts Llc DBA Pastry Art recalls Key Lime and Cream Torte due to undeclared FD&C colors. Products sold after 10/18/2018 may contain Yellow #5 and Blue #1.
Island DessertsApr 22, 2019 - Lower riskFood
Gianni's Fine Food recalls Blue cheese & toasted walnut garlic balsamic vinaigrette, packaged in 6.3-fl. oz. glass bottle. The label is read in
Gianni's Fine Food recalls blue cheese & toasted walnut garlic balsamic vinaigrette due to label not declaring milk in ingredients. Consumers should check for the specific bottle size and label format described.
Gianni's Fine FoodApr 22, 2019 - Use cautionVehicle
FOREST RIVER FLAGSTAFF (2019) recall — Electrical System
Forest River recalls 2019 Flagstaff trailers with improperly installed AC wiring that could melt and cause fire. Owners must have wiring secured away from heat strips.
Forest RiverApr 19, 2019 - Lower riskMedical device
Philips Healthcare Informatics, Inc. recalls IntelliSpace PACS 4.4, Product number 837507 - Product Usage: intended to be used by trained professionals, including
Philips Healthcare recalls IntelliSpace PACS 4.4 software versions due to potential image corruption during use by medical professionals. Affected versions include 4.4.233.8 through 4.4.552.18 with UDI codes.
Philips HealthcareApr 19, 2019 - Use cautionMedical device
AURIS HEALTH INC recalls Monarch, Aspirating Biopsy Needle, REF: MBR-000012, Rx Only, UDI: B634MBR0000120
Auris Health recalls Monarch aspirating biopsy needles (Rx only) due to reported breakage. Affected lots include RS181129-1 through RS190319-1. Stop using if you have these items.
Auris HealthApr 19, 2019 - Lower riskMedical device
Ethicon, Inc. recalls ETHIBOND EXCEL¿ Polyester Suture-ETHIBOND Green 75cm USP1 Single Armed CT-1 Product Code: X425H Product Usage: ETHIBOND
Ethicon recalls ETHIBOND EXCEL polyester suture (Product Code X42: PBQ426) because it may contain high endotoxin levels. This could pose a risk during medical procedures.
EthiconApr 19, 2019 - Lower riskMedical device
Isopure Corp recalls Acidified Concentrate Distribution and Storage System (ACDS System) with a Finish Thompson Centrifugal Pump Model
Isopure Corp recalls ACDS systems with Finish Thompson pumps due to potential magnet corrosion from uneven encapsulation during manufacturing. Affected units have specific serial numbers and model numbers.
IsopureApr 19, 2019 - Lower riskMedical device
Philips North America, LLC recalls SureSigns VS3 NBP Temp, Product Number 863070. For monitoring the physiological parameters of patients (NBP, SpO2 &
Philips recalls SureSigns VS3 NBP Temp monitors with product number 863070 due to software that fails to measure pulse rates above 240 beats per minute, potentially missing critical patient data.
PhilipsApr 19, 2019 - Lower riskDrug
Pacifico National, Inc. dba AmEx Pharmacy recalls BEVACIZUMAB 1.25 mg/0.05 mL 31G MJ syringe Intravitreal Injection. This biologic product was repackaged by AmEx
AmEx Pharmacy recalls BEVACIZUMAB 1.25 mg/0.05 mL 31G syringes due to difficult delivery system. Recalled lot numbers: 190212AB, repackaged 2/12/2019.
AmEx PharmacyApr 19, 2019 - UnratedDrug
Alvogen, Inc recalls FENTANYL Transdermal System, 12 mcg/h, five (12 mcg/h) systems per carton, Rx only, Distributed by: Alvogen, Inc., Pine
Alvogen recalls 12mcg/h Fentanyl patches due to mix-up with higher-dose 50mcg/h patches. Affected units contain 5 patches per carton labeled 12mcg/h but contain 50mcg/h patches. No remedy specified in recall notice.
AlvogenApr 19, 2019 - Lower riskFood
Glorybee Natural Sweeteners, Inc. recalls Item #13898 Raw California Orange Blossom Honey, packaged in an 18 oz jar with gold metal lid. Retail Jar UPC: 0 30042
Glorybee recalls 18oz jars of Raw California Orange Blossom Honey due to unapproved fumagillin antibiotic residue found in FDA samples. Consumers should avoid using this product.
GlorybeeApr 19, 2019 - Use cautionVehicle
HONDA CLARITY FUEL CELL (2018) recall — Equipment
Honda recalls certain 2017-2018 Clarity Fuel Cell vehicles due to water pump failure that can cause stalling and increase crash risk. Owners will receive free water pump replacements.
HondaApr 18, 2019 - Use cautionVehicle
FORD TRANSIT (2018) recall — Seats
MobilityTrans recalls 2014-2018 Ford Transit and Ram Promaster vehicles with Freedman GO-ES Foldaway Seats. In crashes, seat back movement may increase injury risk. Free repair available.
MobilityTransApr 18, 2019 - Use cautionVehicle
NISSAN ALTIMA (2019) recall — Fuel System, Gasoline
Nissan recalls 2019 Altima vehicles with potential fuel leaks that could cause fire if ignited. Owners must have fuel pump lock ring inspected or replaced at no cost by dealers.
NissanApr 18, 2019 - Use cautionVehicle
CHEVROLET TRAX (2019) recall — Suspension
General Motors recalls certain 2017-2019 Chevrolet Trax vehicles due to potential lower-control arm separation affecting handling and increasing crash risk. Owners will receive free inspections and replacements.
ChevroletApr 18, 2019 - Use cautionMedical device
Stryker Neurovascular recalls Stryker Neurovascular, AXS Infinity LS Plus Long Sheath, Rx Only, Sterile EO, USA Customer Service 855-91 NEURO
Stryker Neurovascular recalls AXS Infinity LS Plus Long Sheath (70cm, 80cm, 90cm) due to brittle catheter shaft that may fracture during use. Affected medical devices sold in the US.
Stryker NeurovascularApr 18, 2019 - UnratedMedical device
K2M, Inc recalls Fenestrated Taps 4.5mm, 5.5mm, 6.5mm (Ref#5001-90013, 5001-90014, 5001-90015) Product Usage: The K2M Fenestrated Tap
K2M recalls Fenestrated Taps 4.5mm, 5.5mm, 6.5mm (Ref#5001-90013-5001-90015) due to mislabeling. All distributed lots are affected.
K2MApr 18, 2019 - Lower riskMedical device
Terumo Cardiovascular Systems Corporation recalls Terumo Advanced Perfusion System 1 Electronic Patient Gas System, Catalog # 801188, UDI 00886799000588 The electronic
Terumo recalls its Advanced Perfusion System 1 Electronic Patient Gas System (Catalog # 801188) due to potential inaccurate gas flow rates, which could affect patient safety during medical procedures.
TerumoApr 18, 2019 - Use cautionMedical device
Skytron, Div. The KMW Group, Inc recalls Skytron Integrity 270 Steam Sterilizer and Skytron Integrity 270VP Steam Product Usage: The SKYTRON Integrity 270 Steam
Skytron recalls Integrity 270 Steam Sterilizers with serial numbers 14092619-18113521 due to potential weld failure in air heater assembly. This could cause equipment malfunction in healthcare settings.
SkytronApr 18, 2019 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-421060 Phase 3 Femoral Drill
Zimmer Biomet recalls specific partial knee drill guides due to potential corrosion from incorrect raw materials. Affected items include Lot Numbers ZB160601 to ZB170601. Contact for return instructions.
Zimmer BiometApr 18, 2019 - Lower riskMedical device
Maquet Cardiovascular, LLC recalls Maquet Getinge-BEQ-TOP 5502 ECC Pack Material:701051791R01
Maquet recalls Getinge-BEQ-TOP 5502 ECC packs with batch numbers 3000074733 and 3000081599 due to potential sterility issues after sterilization.
MaquetApr 18, 2019 - UnratedDrug
Torrent Pharma Inc. recalls Losartan Potassium Tablets, USP, 100 mg, a) 90-count (NDC: 13668-115-90), b)1000-count (NDC: 13668-115-10) per bottle,
FDA-confirmed impurity in Torrent Losartan Potassium Tablets may exceed safe levels. Recalled 90-count and 1000-count bottles with specific lot numbers. Stop using immediately if you have these products.
TorrentApr 18, 2019 - Stop using nowConsumer product
Tekno Products Recalls Tuff Smoke-Less Grills Due to Fire and Burn Hazards
Tekno Products recalls Tuff Smoke-Less Grills due to overheating risks. Stop using immediately and return for a full refund.
Tekno ProductsApr 18, 2019 - Stop using nowConsumer product
Target Recalls Wooden Toy Vehicles Due to Choking Hazard
Target recalls Bullseye's Playground wooden toy vehicles due to wheels that can detach, posing a choking hazard to children. Consumers should stop using and return items for a full refund.
Bullseye's PlaygroundApr 18, 2019
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