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
34,959 found- Lower riskDrug
Lannett Company Inc. recalls Oxybutynin Chloride, Extended-Release Tablets USP, 10 mg, 100 Tablet, Rx Only, Distributed by: Lannett Company, Inc,
Lannett recalls 10mg Oxybutynin Extended-Release Tablets (NDC 62175-271-37) due to failed dissolution specifications. Rx-only medication with specific batch numbers and expiration dates.
LannettFeb 21, 2019 - Stop using nowDrug
Macleods Pharma Usa Inc recalls Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/25 mg, 90 count bottles, Rx Only, Manufactured for:
Macleods Pharma recalls 90-count bottles of Losartan Potassium and Hydrochlorothiazide tablets due to carcinogen impurity. Check your lot number.
Macleods PharmaFeb 21, 2019 - Stop using nowDrug
Health Solutions Pharmacy Center Inc dba Professional Compounding Pharmacy recalls PAPAVERINE-PHENTOLAMINE-PGE1 17.44-0.64MG-5.8MCG/ML* INJECTABLE, 5 ml, Professional Compounding Pharmacy, 996 NW Circle
Professional Compounding Pharmacy recalls a sterile injectable drug due to insanitary compounding conditions. Check lot numbers and distribution details.
Professional Compounding PharmacyFeb 21, 2019 - Stop using nowConsumer product
SRAM Recalls Bicycle Gear Hubs Due to Crash and Injury Hazards
SRAM recalls i-Motion 3 coaster brake hubs for bicycles due to brake failure risks. Affected models include Electra Cruiser Custom 3i and other Electra models. Consumers should stop using and contact SRAM for refund instructions.
SRAMFeb 21, 2019 - Stop using nowConsumer product
Shearwater Recalls Diving Transmitters Due to Drowning Hazard
Shearwater yellow diving transmitters may fail to signal tank pressure during dives, risking drowning. Recalled units require immediate stop use and repair or exchange.
ShearwaterFeb 21, 2019 - Use cautionVehicle
PORSCHE 718 CAYMAN (2017) recall — Fuel System, Gasoline
Porsche recalls 2017-2019 718 Cayman models due to potential fuel leaks during crashes that could cause fire. Owners must contact Porsche for free crossmember reinforcement.
PorscheFeb 20, 2019 - Use cautionVehicle
VOLKSWAGEN JETTA (2019) recall — Air Bags
Volkswagen recalls 2019 Jetta vehicles with incorrect driver airbags that may not deploy properly in crashes, risking injury. Owners must contact customer service for free replacement.
VolkswagenFeb 20, 2019 - Use cautionVehicle
PORSCHE CAYENNE (2019) recall — Electrical System
Porsche recalls 2019 Cayenne models with brake pad wear warnings that may not alert drivers, risking loss of vehicle control during braking. Affected owners should contact Porsche for free software update.
PorscheFeb 20, 2019 - Use cautionVehicle
PORSCHE CAYENNE (2019) recall — Suspension
Porsche recalls one 2019 Cayenne Turbo vehicle with potentially loose shock absorbers that could impair steering and increase crash risk. Owners will receive free replacement forks.
PorscheFeb 20, 2019 - Use cautionVehicle
AUDI S5 (2019) recall — Suspension
Audi is recalling 2019 S5 vehicles with potentially loose shock absorbers that could impair steering and increase crash risk. Owners must have shock absorbers replaced free by dealers.
AudiFeb 20, 2019 - UnratedMedical device
Karl Storz Endoscopy recalls FLEXIBLE NEURO-FIBERSCOPE, 3.7MM X 34CM, Model # 11282BN1
Karl Storz recalls FLEXIBLE NEURO-FIBERSCOPE models with incorrect channel port. Affected units have specific serial numbers. No remedy provided in this recall.
Karl Storz EndoscopyFeb 20, 2019 - Lower riskMedical device
Luminex Corporation recalls ARIES HSV 1&2 Assay , REF 50-10017, UDI # 00840487100295
Luminex recalls ARIES HSV 1&2 Assay (REF 50-10017) due to potential partial sealing of side cassette assemblies, which may decrease solution volume and assay sensitivity. Affected units include specific lot numbers with discontinuation dates.
LuminexFeb 20, 2019 - Lower riskMedical device
Ortho-Clinical Diagnostics recalls VITROS¿ 3600 Immunoassay System-Software V3.3.2 & below Product Code: 6802783 For use in the in vitro quantitative,
Ortho-Clinical Diagnostics recalls VITROS 3600 software versions 3.3.2 and below due to potential luminometer malfunction causing inability to process microwell assays. Affected units include specific product codes and serial numbers.
Ortho-Clinical DiagnosticsFeb 20, 2019 - Lower riskMedical device
Abbott Laboratories recalls CELL-DYN Emerald analyzer, REF 09H39-01. The CELL-DYN Emerald is an automated hematology analyzer intended for in-vitro
Abbott recalls CELL-DYN Emerald analyzers with serial numbers below 7765 due to potential QC low results for RBC and PLT. Affected units may need correction to avoid inaccurate blood tests.
AbbottFeb 20, 2019 - UnratedDrug
Vi-Jon, Inc. recalls Topical Solution USP Hydrogen Peroxide First Aid Antiseptic Oral Debriding Agent 32 Fl. Oz. (1 QT) 946 mL bottle,
Vi-Jon recalls 32 fl oz hydrogen peroxide antiseptic solution due to cross contamination with isopropyl alcohol. This may cause unintended effects when used for first aid. No remedy specified in official notice.
Vi-JonFeb 20, 2019 - Lower riskFood
Gilster-Mary Lee Corp. recalls Best Choice Pancake & Waffle Complete Mix Original 32oz. retail carton, 12 retail units per wholesale case. UPC# 70038
Best Choice recalls pancake mix due to undeclared milk. Consumers may face allergic reactions if they have milk allergies. Check UPC 70038 for affected products.
Best ChoiceFeb 20, 2019 - Stop using nowFood
LEAN CULINARY SERVICES, LLC recalls DeliverLean Chicken Salad Triangle Sandwich, Net WT. 7.3 oz (206g)
Lean Culinary recalls chicken salad sandwiches from February 2019 due to Listeria monocytogenes contamination. Consumers should check product date and contact company for details.
Lean CulinaryFeb 20, 2019 - Lower riskFood
Meijer recalls Meijer Ultimate Chocolate Mint Chip Cookie Cookies in clear plastic clamshell 12 count UPC 4125014563 20 count UPC
Meijer recalls 12-count and 20-count chocolate mint chip cookies sold from Feb 6-20, 2019, due to undeclared soy content. Consumers should check UPCs and contact Meijer for details.
MeijerFeb 20, 2019 - Lower riskFood
B&G Foods North America, Inc recalls Victoria Marinara Sauce, 40 oz. (2.5 lb) 1133g, 6Jars / Case
B&G Foods recalls Victoria Marinara Sauce due to potential undeclared cashews. Consumers should check for the specific batch and contact the company for details.
B&G FoodsFeb 20, 2019 - Stop using nowConsumer product
Crate and Barrel Recalls Holiday Milk Bottles Due To Laceration Hazard
Crate and Barrel recalls Holiday Bear Acrylic Milk Bottles due to plastic straws cracking and causing lacerations. Consumers must stop using and get refunds.
Crate and BarrelFeb 20, 2019 - Stop using nowMeat & poultry
Lean Culinary Services, LLC Recalls Ready To Eat Chicken Salad Products Due to Possible Listeria Contamination
Lean Culinary Services recalls ~223 lbs of chicken salad due to possible Listeria contamination. Check dates and discard or return immediately.
DeliverLeanFeb 19, 2019 - Use cautionVehicle
KIA SEDONA (2018) recall — Electrical System
Kia recalls 2018 Sedona vehicles with front passenger seats that may deploy airbags when a child is in a child seat, risking injury. Free repairs to prevent harness breakage.
KiaFeb 19, 2019 - Use cautionVehicle
CROSSROADS REDWOOD (2019) recall — Trailer Hitches
Keystone is recalling 2019 Crossroad Redwood trailers with MORryde Rubber Pin Boxes due to potential trailer separation from tow vehicles, increasing crash risk. Owners can get free bolt tightening at dealers.
KeystoneFeb 19, 2019 - Lower riskMedical device
The Binding Site Group, Ltd. recalls Optilite C-Reactive Protein Kit - Product Usage: The Optilite C-Reactive Protein Reagent is intended for the
The Binding Site recalls Optilite C-Reactive Protein Kits due to potential reagent deterioration causing inaccurate test results. Affected kits include model NK044.OPT.A with lot 437705. Users should contact for guidance.
The Binding SiteFeb 19, 2019 - Lower riskMedical device
Beaver Visitec recalls Micro Knife 5.0mm 30¿, Part Number 0001522 The Beaver¿ Micro Knife 5.0mm 30¿ is a sharp pointed tip intended for
Beaver Visitec recalls Micro Knife 5.0mm 30° with misprinted expiration date on peel pack (lot number 180615). This may cause confusion but does not pose a safety risk.
Beaver VisitecFeb 19, 2019 - Use cautionMedical device
Philips Medical Systems Nederlands recalls Foot Switches used with Philips MultiDiagnost Eleva with Flat Detector; Product Codes: 708037, 708038 Product The
Philips recalls foot switches for MultiDiagnost Eleva with Flat Detector that may bend on non-flat surfaces, causing fluoroscopy image issues. Affected product codes include 708037, 708038.
Philips Medical SystemsFeb 19, 2019 - Lower riskMedical device
Smith & Nephew, Inc. recalls smith&nephew SMF(TM) HIGH OFFSET STIKTITE(TM) COATED STEM 12/14 TAPER -1H SIZE, STEM, REF 713552511
Smith & Nephew recalls specific stem sizes due to incorrect label indicating size 1 instead of -1. This may cause confusion in medical use. Affected items have unique reference numbers.
Smith & NephewFeb 19, 2019 - UnratedDrug
American Health Packaging recalls Lovastatin Tablets USP, 40 mg, packaged in a) 100-count bottles (NDC 68001-316-00) and b)1000-count bottles (NDC
American Health Packaging recalls 40mg Lovastatin Tablets due to impurities in drug substance. This may affect safety. Check NDC codes 68001-316-00 and 68001-316-08 for affected products.
American Health PackagingFeb 19, 2019 - Stop using nowDrug
Leiter's Enterprises, Inc. recalls Cefuroxime 10 mg/mL in Sodium Chloride, Intravitreal injection, 1 mL in a 2mL Vial, Ophthalmic Use Only, Office Use
Leiter's Enterprises recalls 569 vials of Cefuroxime intravitreal injection because it was reconstituted with sterile water instead of sodium chloride.
Leiter's EnterprisesFeb 19, 2019 - Lower riskDrug
Amerigen Pharmaceuticals Inc. recalls Temozolomide Capsules, 5 mg, packaged in a) 5-count bottle (NDC 43975-252-05) b) 14-count bottle (NDC 43975-252-14), Rx
Amerigen Pharmaceuticals recalls 5mg Temozolomide capsules (5-count and 14-count bottles) due to failed dissolution specifications. This is a prescription-only medication.
Amerigen PharmaceuticalsFeb 19, 2019
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