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
34,894 found- UnratedDrug
Odan Laboratories Ltd recalls Day Cream SPF15 Cr¿me de jour FPS 15, { Avobenzone 2%, Octinoxate 7%, Oxybenzone 5%} 15 ml / 0.5 fl. oz jar. Made in
Kamins Dermatologics recalls 21 jars of Day Cream SPF15 due to failed stability specifications. Check lot J146C and expiration date.
Kamins DermatologicsDec 20, 2017 - Lower riskDrug
AuroMedics Pharma LLC recalls Linezolid Injection 600 mg/300 mL (2 mg/mL), 300 mL Single-use, ready-to-use flexible plastic infusion bags in a foil
AuroMedics Pharma recalls Linezolid injection bags with mold particulate matter found in one batch. Stop using affected products immediately to avoid potential health risks.
AuroMedicsDec 20, 2017 - Lower riskFood
NEW SEASONS MARKET recalls Buttermilk Herb Side Salad, prepacked in a clear plastic container, sold by the unit for $2.99, UPC 252326-602998.
NEW SEASONS MARKET recalls Buttermilk Herb Side Salad due to undeclared wheat in croutons. The product was sold with UPC 252326-602998 and may contain wheat without labeling.
NEW SEASONS MARKETDec 20, 2017 - Use cautionVehicle
NEWMAR MOUNTAIN AIRE (2018) recall — Electrical System
Newmar recalls 2016-2018 Mountain Aire motorhomes with loose wiring at the ATS that could cause overheating and fire. Owners must have electrical connection checked by dealers free of charge.
NewmarDec 19, 2017 - Use cautionVehicle
KEYSTONE HIDEOUT (2018) recall — Equipment
Keystone is recalling 2018 Hideout trailers with incorrect tire and weight labels that could lead to tire failure and crashes. Owners must check their Federal Placard for the correct specifications.
KeystoneDec 19, 2017 - Use cautionVehicle
FLEETWOOD DISCOVERY LXE (2018) recall — Electrical System
REV is recalling 2018 Fleetwood Discovery LXE RVs with electrical short risk due to water entering harness connectors. Owners must have harness connectors inspected and fixed free of charge by dealers.
REVDec 19, 2017 - Use cautionVehicle
COACHMEN GALLERIA (2018) recall — Electrical System
Forest River is recalling 2018 Coachmen Galleria motorhomes with faulty lead wires that could overheat and cause fire. Owners must have the lead wire replaced free by dealers.
Forest RiverDec 19, 2017 - Lower riskMedical device
Paragon 28, Inc. recalls P28 JAWS Nitinol Staple System kits are designed for use in an osteotomy, arthrodesis and fragment fixation of bones
Paragon 28 recalls JAWS Nitinol Staple System kits for foot bone repairs due to missing drill guide in some models. Affected kits include specific part numbers and production lots. Consumers should check their kit details and contact Paragon 28 for guidance.
Paragon 28Dec 19, 2017 - Lower riskMedical device
Nipro Medical Corporation recalls Nipro Blood Tubing set with Priming Set and Transducer Protectors. Each device is packaged in a film pouch with 24
Nipro recalls blood tubing sets with possible heparin line occlusion. Affected units include specific model numbers and batch dates. Contact Nipro for details.
NiproDec 19, 2017 - Lower riskMedical device
DeRoyal Industries Inc recalls DeRoyal Sterile Custom kits containing Covidien-Dover(TM) Irrigation Tray with Piston Syringe Containing Medline
DeRoyal recalls sterile surgical kits with Medline Aplicare Povidone Iodine Prep Pads that may expire before the 36-month label date due to a manufacturing issue.
DeRoyalDec 19, 2017 - Use cautionMedical device
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls Implantable Cardioverter Defibrillators (ICDs), Evera MRI. Labeled as the following: a. Evera MRI XT DR ICD DF1
Medtronic recalls specific implantable heart devices (ICDs) due to possible failure to prevent high and low voltage therapy. Affected models include Evera MRI XT DR ICD DF1 and others with listed product numbers and serials.
MedtronicDec 19, 2017 - Lower riskMedical device
LivaNova USA recalls Sorin Group Smart Perfusion Pack E-Pack, REF 088511400, Rev: L, Single Use, Sterile, Rx. The firm name on the label is
LivaNova recalls Smart Perfusion Pack E-Packs with incorrect expiration dates on labels. This may lead to improper use if the product expires before intended use. Affected units include specific model numbers and lots.
LivaNovaDec 19, 2017 - Lower riskMedical device
Cook Inc. recalls Norm-Ject Tuberkulin Syringe, Catalog Number: K-ATS-1000, Global Product Number: G19871 Product Usage: Used to place in
Cook recalls Norm-Ject Tuberkulin Syringes (Catalog K-ATS-1000) used in IVF procedures due to potential nonviable gametes or embryos from incomplete quality testing.
CookDec 19, 2017 - Lower riskMedical device
Ventana Medical Systems Inc recalls ultraView Universal DAB Detection Kit, Ventana part Number 760-500, Roche GMMI 05269806001 in vitro diagnostic
Ventana recalls ultraView Universal DAB Detection Kit (part 760-500) due to leaking and sticking reagent dispensers. Affected units have specific lot numbers and UDI codes. Stop using immediately to prevent potential contamination.
VentanaDec 19, 2017 - Lower riskMedical device
PerkinElmer Health Sciences, Inc. recalls PerkinElmer 226 Sample Collection Device
PerkinElmer recalls 226 Sample Collection Devices with serial numbers that don't match pack labels. Affected units have specific serial ranges and lot numbers. Consumers should check their device details.
PerkinEl:merDec 19, 2017 - Lower riskDrug
Unichem Pharmaceuticals Usa Inc recalls Divalproex Sodium Delayed Release Tablets USP, 500 mg, 100-count bottle, RX Only, Manufactured by: Unichem Laboratories
Unichem Pharmaceuticals recalls 500mg Divalproex Sodium tablets due to metronidazole powder cross contamination. This could cause unintended medication interactions. Return to Unichem for replacement.
UnichemDec 19, 2017 - UnratedFood
KOTECHA BROTHERS, LLC. recalls Haldiram's Fresh Paneer Traditional Indian Soft Cottage Cheese, Net Weight 800g (28.2 oz)
Haldiram's Fresh Paneer Traditional Indian Soft Cottage Cheese (800g) recalled due to Listeria monocytogenes detected in a sample. Consumers should check batch numbers and contact the manufacturer for details.
Kotecha BrothersDec 19, 2017 - UnratedFood
Fresh Pak, Inc. recalls 7oz Fruit and cheese Snacks - no brand. 1 unit per case
Fresh Pak recalls 7oz Fruit and Cheese Snacks (UPC 7122817684) due to potential Listeria monocytogenes contamination. Affected lots: 312422, 312511, 312641, 312755, 312918. Use by dates Dec 17-21.
Fresh PakDec 19, 2017 - Lower riskFood
New Punjab Sweets Inc. recalls Sakkar Para, 1 lb. clear plastic clamshell containers.
New Punjab Sweets recalls Sakkar Para 1 lb clear plastic clamshell containers due to undeclared wheat and milk allergens. Consumers should check product labels for these ingredients.
New Punjab SweetsDec 19, 2017 - Use cautionConsumer product
Superior Importers Recalls Mattresses Due to Violation of Federal Mattress Flammability Standard; Sold Exclusively at Amazon.com
Superior Importers recalls Home Life mattresses sold on Amazon for failing federal flammability standards, risking fire. Consumers must stop using and get free cover to comply.
Superior ImportersDec 19, 2017 - Stop using nowConsumer product
Squatty Potty Recalls Children's Toilet Step Stools Due to Injury and Fall Hazards
Squatty Potty recalls children's toilet step stools because the top hat can detach, causing falls. Stop using immediately and contact the company for a refund.
Squatty PottyDec 19, 2017 - Stop using nowConsumer product
Monte Carlo Recalls Ceiling Fans Due to Injury Hazard
Monte Carlo recalls two ceiling fan models with 5 blades due to bracket failure causing blade falls and injury risk. Consumers must stop using and get free bracket replacement kits.
Monte CarloDec 19, 2017 - Stop using nowConsumer product
Matrix Fireworks Recalls Fireworks Due to Violation of Federal Standard; Explosion and Burn Hazards
Jumbo Fireworks 'Surprise Fountain' recalled for explosion and burn hazards. Return to place of purchase for a full refund.
Jumbo FireworksDec 19, 2017 - Use cautionVehicle
MERCEDES-BENZ AMG GT (2017) recall — Air Bags
Mercedes-Benz is recalling 2017 AMG GT vehicles with AMG Performance Seats due to potential passenger airbag incorrect activation or deactivation in crashes, risking injury. Owners will receive free seat cushion replacements by February 2018.
Mercedes-BenzDec 18, 2017 - Use cautionVehicle
FORD ESCAPE (2018) recall — Air Bags
Ford is recalling 2018 Escape vehicles with side curtain air bags that may detach during deployment, posing injury risks. Owners should contact Ford for free replacement of affected air bags.
FordDec 18, 2017 - Use cautionVehicle
FORD MUSTANG (2018) recall — Electrical System
Ford recalls 2018 Mustangs with automatic transmission and digital dash that may roll away without warning if not parked. Fix involves software update by February 5, 2018.
FordDec 18, 2017 - Lower riskMedical device
Roche Diagnostics Corporation recalls c6000, Chemistry (Photometric, Discrete), for clinical use. - cobas e 601 module: Immunoassay Analyzer, Catalog
Roche recalls cobas e 601 modules for clinical use due to potential inaccurate test results when 13 sample tubes are used without adapters.
RocheDec 18, 2017 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls ADVIA Centaur TSH3-Ultra (Thyroid Stimulating Hormone 3 Ultra), Catalog Numbers: 06491072 (100 tests), 06491080 (500
Siemens Healthcare recalls ADVIA Centaur TSH3-Ultra thyroid tests with specific catalog numbers and lot numbers due to potential reduced dilution recovery or inoperability when used with certain reagents.
Siemens HealthcareDec 18, 2017 - Use cautionMedical device
Terumo Cardiovascular Systems Corp recalls Terumo Cardiovascular Procedure Kits containing Pall LG6NS LeukoGuard¿ Leukocyte Reduction Arterial Blood Filters. The
Terumo recalls procedure kits with Pall LG6NS LeukoGuard arterial blood filters due to possible blood leaks. Affected kits may cause bleeding risks during heart surgery. Consumers should contact Terumo for details.
TerumoDec 18, 2017 - Lower riskMedical device
Johnson & Johnson Vision Care, Inc. recalls ACUVUE OASYS for ASTIGMATISM Brand Contact Lenses. Lot no. B00NKM0G. Base Curve 8.6, Refractive Power -3.00D-1.25/90.
Johnson & Johnson Vision Care recalls ACUVUE OASYS contact lenses with lot number B00NKM0G due to potential package integrity failure observed during testing. Consumers should check their lenses for the specific lot number and model details.
Johnson & Johnson Vision CareDec 18, 2017
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