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
34,943 found- Use cautionVehicle
CHRYSLER PACIFICA (2019) recall — Electrical System
Chrysler is recalling 2018-2019 Pacifica models due to a powertrain control module issue that can cause vehicle stalls, increasing crash risk. Owners must contact Chrysler for free replacement.
ChryslerSep 8, 2018 - Use cautionMedical device
Vital Scientific N.V. recalls V-Twin, Catalog # 6002-800, UDI: 03661540600180 - Product Usage: An in vitro diagnostic device, which is an automated
Vital Scientific recalls V-Twin diagnostic devices with serial numbers 14-3301-14-3344, 15-3301-15-3326, 16-3301-16-3353, 17-3301-17-3346, 18-3301-18-3323 due to improper cooling indicator installation that may cause reagent storage issues.
Vital ScientificSep 7, 2018 - Lower riskMedical device
Bayer Medical Care, Inc. recalls Codan Filter (Codan catalog number BC 693) used with Medrad Patient Administration Sets (PAS) and Intego PET Infusion
Bayer recalls Codan Filter (BC 693) used with Medrad PAS and Intego PET Infusion systems due to potential loose particulate when dust cap is removed. Affected batch numbers listed in product description.
BayerSep 7, 2018 - Use cautionMedical device
Abbott Laboratories, Inc recalls APS Accelerator modular systems, 208-230 V-, 50/60 Hz, 1800 VA, IVD, RX, Class 2 Laser Product,
Abbott recalls APS Accelerator modular systems with missing safety pacemaker labels. These systems require 200mm distance from pacemaker users to prevent malfunction risks.
AbbottSep 7, 2018 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Dimension Vista Lipase Flex Reagent Cartridge, Model Number 10461745 Product Usage: Dimension Vista - The LIPL method
Siemens Healthcare recalls Dimension Vista Lipase Flex Reagent Cartridges (model 10461745) with specific lot numbers due to potential QC and patient result variability. Affected units may not provide accurate test results.
Siemens HealthcareSep 7, 2018 - Lower riskDrug
Noven Pharmaceuticals, Inc. recalls Minivelle (estradiol transdermal system) Patches, Delivers 0.025 mg/day, 8 count boxes, Rx only, Mfd. by: Noven
Noven Pharmaceuticals recalls Minivelle estradiol patches due to adhesive issues that may cause inconsistent hormone delivery. Affected products include 8-count boxes with specific NDC and expiration dates. Consumers should contact Noven for details.
NovenSep 7, 2018 - Stop using nowFood
Shearers Foods, Llc recalls White Corn Tortilla Chips packaged under the following brand names and sizes: 1. Shearer's White Restaurant Style Bulk,
Shearers Foods recalls White Corn Tortilla Chips due to possible metal contamination. Affected products include Shearer's White Restaurant Style Bulk and other brands sold from December 2018 to February 2019.
Shearers FoodsSep 7, 2018 - Lower riskFood
Gravel Ridge Farms recalls Shelled eggs in blank cardboard cases at 2.5 dozen a case. Shelled eggs in dozen cartons labeled as "Gravel Ridge Farms
Gravel Ridge Farms recalls shelled eggs in specific cardboard cases due to salmonella contamination. Products with expiration dates from July 2018 to October 2018 are affected. Consumers should check labels for the listed case and carton identifiers.
Gravel Ridge FarmsSep 7, 2018 - Lower riskFood
Market of Choice Inc recalls Sesame Noodle Salad Vegan, packaged in 8 oz. or 16 oz. plastic container. UPC of 8 oz. container: 0 211630 203994. UPC
Market of Choice recalls Sesame Noodle Salad Vegan products due to undeclared egg. Products sold between August 2018 and September 2018 contain wheat and soy but no egg declared on label.
Market of ChoiceSep 7, 2018 - Use cautionMedical device
Stryker Medical Division of Stryker Corporation recalls Altrix¿ Precision Temperature Management System Model: 8001Product Usage: The Altrix system is intended for circulating
Stryker recalls Altrix Model 8001 units made between Oct 2016 and June 2017 due to potential alarm fatigue and device faults that could affect patient temperature monitoring.
StrykerSep 6, 2018 - Lower riskMedical device
CryoLife, Inc. recalls CryoPatch SG Pulmonary Hemi-Artery, 1 graft
CryoLife recalls SG Pulmonary Hemi-Artery grafts with incorrect labeling of conduit and branch lengths. This labeling error may cause improper use during medical procedures.
CryoLifeSep 6, 2018 - Lower riskMedical device
Stihler Electronic Gmbh recalls Heating Profile PRISMAFLO II S blood return warmer for Prismaflex Product Code: PF2-WP31 Product Usage: The PRISMAFLO
Stihler recalls PRISMAFLO II S blood return warmers (Product Code PF2-WP31) due to risk of low-level skin burns from hotspots. Affected units have serial number E22368.
StihlerSep 6, 2018 - Lower riskMedical device
Implant Direct Sybron Manufacturing, LLC recalls Implant Direct Scan Adapter Assembly Replant platform for the following part numbers: 6035-09PT-M (3.5mmD)/UDI :
Implant Direct recalls scan adapter assemblies with part numbers 6035-09PT-M, 6043-09PT-M, and 6050-09PT-M that may cause scanning delays due to incorrect assembly. Affected units include specific lot numbers and part numbers listed in the recall notice.
Implant DirectSep 6, 2018 - UnratedDrug
Par Pharmaceutical, Inc. recalls Pramipexole dihydrochloride extended release tablets, 0.75 mg, packaged in 30-count bottles, Rx only, Manufactured by:
Par Pharmaceutical recalls 30-count 0.75mg Pramipexole dihydrochloride extended release tablets with impurities that may affect safety. Check NDC 10370-252-11 and lot numbers for affected batches.
Par PharmaceuticalSep 6, 2018 - Lower riskDrug
Baxter Healthcare Corporation recalls 0.9% Sodium Chloride Injection USP 50 mL Viaflex container Baxter Healthcare Corporation Deerfield, IL 60015 -- NDC
Baxter Healthcare recalls 0.9% Sodium Chloride Injection 50mL Viaflex containers due to a cGMP deviation. Affected lots may have quality issues affecting safety.
Baxter HealthcareSep 6, 2018 - Stop using nowDrug
InvaGen Pharmaceuticals, Inc. recalls Bupropion Hydrochloride ER Tablets, USP 150 mg, packaged in a) 90-count bottle (NDC 69097-875-05), Manufactured for:
InvaGen Pharmaceuticals recalls 150mg Bupropion ER tablets with impurities from batches older than 18 months. These tablets may contain harmful levels of meta-chlorobenzoic acid, posing a risk of serious injury if taken.
InvaGenSep 6, 2018 - Stop using nowConsumer product
TJX Recalls Barstools Due to Fall Hazard; Sold at HomeGoods, Marshalls and T.J. Maxx Stores
TJX recalls swivel barstools with beige, blue, or gray fabric backs that can break at wood joints, causing falls. Return to Home Goods, Marshalls, or T.J. Maxx for full refunds.
TJXSep 6, 2018 - Stop using nowConsumer product
Lester Electrical Recalls Links Series Chargers Due to Fire and Burn Hazards
Lester Electrical recalls Links Series chargers (models 28080, 28090, 28100) used with golf carts due to fire and burn risks from overheating control boards.
Lester ElectricalSep 6, 2018 - Stop using nowMeat & poultry
Wayne Farms, LLC Recalls Fully Cooked Chicken Products due to Possible Foreign Matter Contamination
USDA recalls 438,960 pounds of Wayne Farms fully cooked chicken products that may contain metal pieces. Consumers are urged not to eat these items and should throw them away or return to store.
Wayne FarmsSep 5, 2018 - Stop using nowMeat & poultry
New York Style Sausage Co. Recalls Raw Chorizo Sausage Products due to Misbranding and an Undeclared Ingredient
New York Style Sausage Co. recalls raw Salvadoran chorizo due to undeclared sesame seeds. Do not consume; discard or return immediately.
New York Style Sausage Co.Sep 5, 2018 - Use cautionMeat & poultry
Caito Foods, LLC Recalls Chicken Salad Products due to Misbranding and an Undeclared Allergen
USDA recalls 242 pounds of chicken salad products from Caito Foods due to undeclared tree nuts (walnuts) on labels. Consumers urged to stop using these products immediately.
Caito FoodsSep 5, 2018 - Lower riskMedical device
BioFire Diagnostics, LLC recalls FilmArray Blood Culture Identification (BCID), IVD, Rx Only, BioFire Diagnostics, LLC, Panel Catalog Numbers/ UDI:
BioFire Diagnostics recalls FilmArray Blood Culture Identification kits that may give false positive results for Proteus when used with certain blood culture bottles. Affected kits include specific catalog numbers and bottle types.
BioFire DiagnosticsSep 5, 2018 - Use cautionMedical device
Thoratec Switzerland GMBH recalls Thoratec CentriMag Motor, Model: 102956, a component of the Thoratec CentriMag Blood Pumping System and PediMag Blood
Thoratec recalls CentriMag Motor Model 102956 due to reports of motor stopping from wire breaks or short circuits. Affected units have serial numbers until design change.
ThoratecSep 5, 2018 - Stop using nowMedical device
Cordis Corporation recalls Cordis POWERFLEX PRO PTA Dilatation Catheter - Product Usage: Is intended to dilate stenoses in iliac, femoral,
Cordis recalls POWERFLEX PRO PTA Dilatation Catheters due to potential burst shaft failure during use. Affected units have specific catalog and lot numbers. Stop using immediately if you own one.
CordisSep 5, 2018 - Lower riskFood
Wismettac Asian Foods (USA) dba Nishimoto Trading Co Ltd recalls EVERYBURGER - Burger-Shaped Chocolate Cookies: NET WT. 2.32 oz. (66 g) There are 2 packing sizes; 10 items per case and
Nishimoto Trading recalls Everyburger chocolate cookies (2.32 oz) for partial allergen labeling on nutrition stickers. Consumers should check packaging for 10 or 80-piece cases.
Nishimoto TradingSep 5, 2018 - Lower riskFood
Elaboraciones Felo, Inc. recalls Super Pizza Turnover, Elaboracion Felo, Inc. Avenida Yumet No. 112, Aguadilla, PR 00603
Elaboraciones Felo recalls Super Pizza Turnover due to failure to declare soy and sulfites allergens. Consumers should check packaging for ink-stamped production date and shift.
Elaboraciones FeloSep 5, 2018 - Use cautionConsumer product
Rust-Oleum Recalls Countertop Coating Due to Violation of Federal Lead Paint Ban
Rust-Oleum recalls black satin countertop coating with lead levels exceeding federal limits. Lead exposure risks health issues, especially for children. Consumers get refunds or repair kits.
Rust-OleumSep 5, 2018 - Stop using nowConsumer product
Polaris Recalls Ranger Recreational Off-Highway Vehicles Due to Crash Hazard (Recall Alert)
Polaris recalls 2018 Ranger 500, 570, EV and EV LI-ION models due to front control arms that can separate, causing crashes. Owners must stop using and contact a dealer for free repair.
PolarisSep 5, 2018 - Stop using nowConsumer product
Hawthorne Hydroponics Recalls Humidifiers Due to Fire and Shock Hazards
Hawth: Ideal-Air 175-pint industrial humidifiers recalled due to overheating fire and shock risks. Return for store credit refund.
Hawthorne HydroponicsSep 5, 2018 - Use cautionMeat & poultry
Bahar LLC Recalls Frozen, Raw Beef Dumpling Products Produced without Benefit of Inspection
USDA FSIS recalls 2,520 pounds of frozen raw beef dumplings made without federal inspection. Consumers urged not to eat these products; discard or return to retailer.
BaharSep 4, 2018
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