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
34,893 found- Lower riskMedical device
Kentec Medical Inc recalls POLYURETHANE ENFit(R) AMERITUS NG FEEDING TUBE, REF Numbers: a) ENF-50P-40 b) ENF-50P-50 c) ENF-50P-80 d) ENF-60P-40 e)
Kentec Medical recalls pediatric ENFit feeding tubes with inadequate radiopaque stripes for X-ray detection. This may cause misdiagnosis during medical imaging. Affected tubes have specific reference numbers and lot numbers listed.
Kentec MedicalJun 23, 2017 - Lower riskMedical device
International Medsurg Connection, Inc. recalls Piston Syringe, 10 CC L/S, 100 per box, 12 boxes/case, 1,200/case The products are used to inject fluids into, or
Recalled International Medsurg Piston Syringes (10 CC L/S) due to insufficient documentation supporting sterility claims. Affected units include specific lot numbers from 2012-2017. Consumers should contact the manufacturer for details.
International MedsurgJun 23, 2017 - UnratedDrug
ImprimisRx CA, Inc., dba ImprimisRx recalls Latanoprost PF Solution, 0.005%, Ophthalmic Drops in Sterile 5ml Bottles, Compounded for a licensed professional or
ImprimisRx recalls 0.005% Latanoprost PF eye drops compounded for professionals due to use of non-pharmaceutical grade PEG 40 Castor Oil. This may pose safety risks for users.
ImprimisRxJun 23, 2017 - Use cautionVehicle
JAGUAR XJ (2011) recall — Air Bags
Jaguar recalls 2010-2011 XJ vehicles with potential air bag calibration issues that could increase crash injury risk. Owners must update RCM software at dealerships.
JaguarJun 22, 2017 - Use cautionVehicle
MAZDA MAZDA3 (2016) recall — Parking Brake
Mazda recalls 2016 Mazda3s with potential parking brake issues causing unintended vehicle movement on slopes, increasing crash risk. Owners must contact Mazda for free repairs once parts are available.
MazdaJun 22, 2017 - Lower riskMedical device
NeuroLogica Corporation recalls The GC80 Digital X-ray Imaging System
NeuroLogica recalls GC80 Digital X-ray Imaging System due to overexposure risk during thorax exams. Affected units may produce unsafe images; contact for details.
NeuroLogicaJun 22, 2017 - Stop using nowMedical device
Quidel Corporation recalls InflammaDry(R) AN RPS DIAGNOSTIC SOLUTION, Sample Collectors InflammaDry(R) is a rapid, immunoassay test for the
Quidel recalls InflammaDry Sample Collectors with plastic spurs that could cause injury during use. Affected lots 1705405 and 170:1705359. Stop using immediately.
QuidelJun 22, 2017 - Use cautionMedical device
Avid Medical, Inc. recalls AVID TruCustom DAVINCI PACK convenience kits, Item Code: ADVU037-09
Avid Medical recalls specific DAVINCI PACK convenience kits that may contain loose polypropylene foreign material, posing a potential risk during medical use.
Avid MedicalJun 22, 2017 - Lower riskMedical device
Medtronic Perfusion Systems recalls DLP Pressure Disposable Pressure Display Sets Extends the pressure line in order to reach the pressure monitoring unit
Medtronic Perfusion Systems recalls DLP Pressure Disposable Pressure Display Sets with small pinholes in sterile pouch packaging. Seven product models affected. No remedy specified.
Medtronic Perfusion SystemsJun 22, 2017 - UnratedDrug
Lupin Pharmaceuticals Inc. recalls Paroxetine Extended-Release Tablets USP, 12.5 mg, 30 count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals,
Lupin Pharmaceuticals recalls 12.5mg Paroxetine Extended-Release Tablets due to failed dissolution testing. Affected lots manufactured between Nov 2018 and March 2019. No specific remedy stated in recall notice.
Lupin PharmaceuticalsJun 22, 2017 - UnratedDrug
Vitility recalls MAN OF STEEL capsules, 3000mgs/grain, 1-count packets, Packaged for: One Drop Solutions, LLC, POB 231693, Sacramento,
FDA recalls Vitility's MAN OF STEEL capsules (3000mgs/grain) due to undeclared sildenafil, an unapproved drug with unknown safety.
VitilityJun 22, 2017 - UnratedDrug
Advanced Pharma Inc. recalls QUELICIN (Succinylcholine Chloride) Injection, USP 20 mg/mL in a) 5 mL vial (NDC 15082-814-67), b) 7mL vial (NDC
Advanced Pharma recalls QUELICIN (Succinylcholine Chloride) 20 mg/mL injections with potential lack of sterility. Affected lots from May 2017 to July 2017. Consumers should contact the manufacturer for details.
Advanced PharmaJun 22, 2017 - Lower riskFood
McCain Foods Canada, Inc. recalls MCCAIN ONION RING BATTERED PORTION PERFECT ¿ 60X4 oz
McCain Foods Canada recalls frozen onion ring batter portions due to undeclared milk in raw ingredients. Consumers should check lot codes for affected items and avoid consumption if allergic to milk.
McCain FoodsJun 22, 2017 - Lower riskFood
Sami's Pita Bakery, Inc. recalls SAMI'S BAKERY, Peanut Butter Cookies, Net Wt. 7oz. (196g), Packed by: Sami's Pita Bakery Inc., Tampa, FL.
Sami's Bakery recalls peanut butter cookies due to undeclared milk allergen. Consumers should check product labels for milk content.
Sami's BakeryJun 22, 2017 - Use cautionVehicle
ASTON MARTIN V8 VANTAGE (2012) recall — Power Train
Aston Martin is recalling 2012 V8 Vantage vehicles with 6-speed Auto-Shift Manual transmissions due to potential hydraulic fluid leaks causing transmission shift failures and vehicle rollaways.
Aston MartinJun 21, 2017 - Use cautionVehicle
ASTON MARTIN V8 VANTAGE (2012) recall — Electrical System
Aston Martin recalls 2011-2012 V8 Vantage vehicles due to transmission shifting issues. Dealers will reinstall clutch system software free of charge.
Aston MartinJun 21, 2017 - Use cautionVehicle
ASTON MARTIN V8 VANTAGE (2012) recall — Power Train
Aston Martin recalls 2011-2014 V8 Vantage models with SportShift II transmissions due to potential hydraulic fluid leaks causing transmission shift issues and vehicle rollaway risks.
Aston MartinJun 21, 2017 - Lower riskMedical device
Elekta, Inc. recalls MOSAIQ(R) Oncology Information System, Versions 2.50.05 and higher Product Usage: MOSAIQ¿ is an oncology information
Elekta recalls MOSAIQ Oncology Information System versions 2.50.05+ due to outdated information retention in order sets, potentially affecting treatment planning accuracy.
ElektaJun 21, 2017 - Lower riskMedical device
B. Braun Medical, Inc. recalls Spinal & Epidural Anesthesia Tray. Product Catalog Number: 555172. Local anesthesia of the skin prior to insertion of
B. Braun Medical recalls spinal and epidural anesthesia trays with loose polypropylene foreign matter that may cause contamination during procedures.
B. Braun MedicalJun 21, 2017 - UnratedMedical device
Valorem Surgical LLC recalls PALLAS M/MAXIMIS 350 Straight Rod. Part of MAXIMIS Pedicle Screw Spinal Fixation System. Valorem Surgical, Chicago, IL.
Valorem Surgical recalls PALLAS M/MAXIMIS 350 Straight Rod due to quality system inconsistencies. Affected units were sold through 2015 for spinal fixation. No specific remedy is listed in the recall notice.
Valorem SurgicalJun 21, 2017 - UnratedDrug
SCA Pharmaceuticals recalls Potassium PHOSphate added to 250 mL 0.9% Sodium Chloride 15 mMol (22 mEq K+) Total Approximate Volume 255 mL, Rx only,
SCA Pharmaceuticals recalls Potassium Phosphate added to 0.9% Sodium Chloride solution due to lack of sterility assurance. This medication is for prescription use only and may pose infection risks if used.
SCA PharmaceuticalsJun 21, 2017 - Lower riskFood
Cracker King Corp. recalls Cristina brand Egg Crackers (Galletas de Huevo), 4OZ, Clear plastic/film type bag, ready-to-eat, dry/ambient storage
Cracker King recalls Cristina Egg Crack: 4oz clear bags with undeclared soy lecithin. Consumers should check product labels for soy lecithin and contact Cracker King for details.
Cracker KingJun 21, 2017 - UnratedFood
The Smokehouse of New York, LLC. recalls The Smokehouse of NY Smoked Norwegian Fish packaged as: 4oz & 8oz and whole sides
The Smokehouse of NY recalls smoked Norwegian fish products (4oz, 8oz, whole sides) with potential Listeria monocytogenes contamination. Consumers should check lot numbers 124-157 for affected items.
The Smokehouse of NYJun 21, 2017 - Use cautionFood
Texas Plum Line recalls Wild Plum Apricot Bread 16 oz packaged in a glass jar
Texas Plum Line recalls 16 oz Wild Plum Apricot Bread in glass jars due to undeclared milk. Check your labels for allergen info.
Texas Plum LineJun 21, 2017 - Use cautionMeat & poultry
Channel Fish Processing Co., Inc. Recalls Siluriformes Fish Products Due To Misbranding and Undeclared Allergens
USDA FSIS recalls Channel Fish Processing Co. products due to undeclared milk allergens in breaded Swai fillets. Consumers urged to stop using these products immediately.
ChannelJun 20, 2017 - Lower riskMeat & poultry
Embutidos Fanguito, Inc. Recalls Pork Products Due To Mislabeling, Misbranding, and Undeclared Allergens
USDA FSIS recalls 984 pounds of pork products from Embutidos Fanguito due to mislabeling, misbranding, and undeclared allergens like soy and MSG.
Embutidos FanguitoJun 20, 2017 - Stop using nowVehicle
KTM 690 DUKE (2017) recall — Fuel System, Gasoline
KTM recalls 2016-2017 690 Duke motorcycles with potential fuel leaks from filler cap area, risking fire or injury. Contact KTM customer service for remedy.
KTMJun 20, 2017 - Lower riskMedical device
Beckman Coulter Inc. recalls UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System, Software Version 3.2. The DxH Slidemaker Stainer allows
Beckman Coulter recalls UniCel DxH Slidemaker Stainer software version 3.2 due to potential leakage from a fitting that may not seal after installation. This affects blood analysis systems used in labs.
Beckman Coul: A short, human brand name for headings (e.g.Jun 20, 2017 - Use cautionMedical device
Hamilton Medical, Inc. recalls Intellicuff Standalone (PN 951001) Used to continuously measure and automatically maintain the user-set cuff pressure
Hamilton Medical recalls Intellicuff Standalone (PN 951:1000-2090) due to risk of motor failure during use. This device measures and maintains cuff pressure for ventilated patients. Affected units may stop functioning, requiring immediate action.
Hamilton MedicalJun 20, 2017 - Lower riskMedical device
Keystone Dental Inc recalls Multi-Unit Abutment Angled, 17¿, 4mm Cuff 4.1/4.5mm TiLobe¿ Implants, Catalog Number 45324K pRODUCT Usage: Use in
Keystone Dental recalls specific dental implants due to abutments failing to accept final screws. Affected units have catalog number 45324K and lot 33006.
Keystone DentalJun 20, 2017
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