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Latest recalls
35,025 found- Use cautionMeat & poultry
FSIS Issues Public Health Alert for Raw Ground Beef Product Due to Possible E. Coli O157:H7 Contamination
FSIS recalls raw ground beef from Greater Omaha Packing Co. produced Jan 14, 2021, with possible E. coli O157:H7 contamination. Discard or return products purchased between Jan 28-31, 2021, from Art's Food Market in Sandwich, Illinois.
Greater Omaha Packing CoFeb 2, 2021 - Use cautionVehicle
SPARTAN K2 (2020) recall — Steering
Shyft Group recalls certain 2020-2021 RV Chassis K2, K3, K4 vehicles due to steering gear fasteners potentially loosening and causing steering difficulty, increasing crash risk. Owners must have fasteners replaced free of charge.
Shyft GroupFeb 2, 2021 - Lower riskMedical device
Alcon Research, LLC recalls Alcon Custom Ophthalmic Surgical Procedure Packs
Alcon Research LLC
Alcon Research LLCFeb 2, 2021 - Lower riskMedical device
Philips North America Llc recalls IntelliVue MX40 Patient Monitor, Model Number: 865350 (US) 865352 (OUS) Software version number B.06.59 - Product
Philips recalls IntelliVue MX40 Patient Monitors with specific model numbers and software versions due to manufacturing defects that could lead to potential device failure in hospital use.
PhilipsFeb 2, 2021 - Lower riskDrug
Teligent Pharma, Inc. recalls Betamethasone Dipropionate Ointment USP, 0.05% (Augmented), packaged in 15 grams tubes, Manufactured by: Teligent
Teligent recalls Betamethasone Dipropionate Ointment 0.05% (Augmented) tubes due to impurities that could cause harm. Affected lots from 2021-2022.
TeligentFeb 2, 2021 - Lower riskDrug
Apotex Corp. recalls Enoxaparin Sodium Injection, USP 100 mg/mL Single Dose Syringes with Automatic Safety Device For Subcutaneous Injection
Apotex recalls 10x1mL Enoxaparin syringes with incorrect labeling that may cause dosing errors. Affected units have 150mg/mL markings instead of 100mg/mL. Contact for return instructions.
ApotexFeb 2, 2021 - Stop using nowFood
Ohio Hickory Harvest Brand Products, Inc. recalls Sprout's Vanilla Flavored Yogurt Covered Cranberries UPC 646670463778 12 Ounce Stand-Up Pouch Bag Ambient Storage
Sprout's Vanilla Flavored Yogurt Covered Cranberries recalled due to undeclared tree nuts (almonds). Check your UPC and batch number.
Sprout'sFeb 2, 2021 - Lower riskMedical device
Thermo Fisher Scientific recalls Cascadion SM Clinical Analyzer, REF 99990000 SN Type: 9910
Thermo Fisher recalls Cascadion SM Clinical Analyzer (SN 9910) due to software defect causing false Vitamin D results. Affected units may indicate severe Vitamin D deficiency. No remedy specified in recall notice.
Thermo FisherFeb 1, 2021 - Lower riskMedical device
Epimed International, Inc. recalls Feth-R-Kath Catheter, 19g x 24". Intended Use:Radlo Opaque Epidural Catheter Catalog #: 157-1924 Intended for epidural
Epimed recalls 19g x 24" epidural catheters (catalog #157-1924) due to potential coating cracking. Affected units have specific lot numbers. Contact for return instructions.
EpimedFeb 1, 2021 - Lower riskMedical device
Bovie Medical Corporation recalls ConMed Disposable Bipolar Ablators - Product Usage: intended to be used for cutting, vaporization, and coagulation of
Bovie Medical recalls specific ConMed Disposable Bipolar Ablators due to potential pinholes in sterile packaging that could compromise sterility during surgery.
BovieFeb 1, 2021 - Lower riskMedical device
Insulet Corporation recalls Omnipod DASH Insulin Management System User Guide (OUS Only) Product Catalog Number: PT 000002 XXX XXX XX PT 000318 PT
Insulet recalls Omnipod DASH insulin management system user guides with a misprint that could cause incorrect insulin doses and hypoglycemia for users outside the US. Affected guides include specific language versions sold in Canada, Germany, France, and other countries.
InsuletFeb 1, 2021 - Lower riskDrug
Kimberly-Clark Corporation recalls Scott¿ Moisturizing Foam Hand Sanitizer, 1.2 Liters (40.5 fl oz), Distributed in the U.S. by Kimberly-Clark Global
Kimberly-Clark recalls Scott Moisturizing Foam Hand Sanitizer due to incorrect labeling with some bottles containing Foam Skin Cleanser soap.
Kimberly-ClarkFeb 1, 2021 - Lower riskFood
KEWPIE TRADING EUROPE B.V. recalls Kewpie Deep Roasted Sesame Dressing; 8 oz.(263ml/243g) and 64 oz. (1893 ml/1950g) bottles (glass and plastic)
Kewpie recalls deep roasted sesame dressings that exceeded EU pesticide limits. Check UPCs and lot codes for affected bottles. No action needed if product is unopened.
KewpieJan 31, 2021 - Use cautionVehicle
TESLA MODEL S (2014) recall — Back Over Prevention
Tesla recalls 2014 Model S vehicles with center display using 8GB eMMC NAND flash memory. The recall addresses potential loss of rearview camera, defrost settings, and turn signals due to eMMC wear-out, increasing crash risk. Owners must update firmware or get free replacement.
TeslaJan 29, 2021 - Use cautionVehicle
MERCEDES-BENZ AMG A35 (2021) recall — Child Seat
Mercedes-Benz USA is recalling 2021 A35 AMG vehicles with missing ISOFIX bracket anchoring bars. This could cause child seat detachment during a crash, increasing injury risk. Owners must have brackets inspected and replaced by dealers.
Mercedes-BenzJan 29, 2021 - Use cautionVehicle
BMW X5 (2021) recall — Steering
BMW is recalling certain 2021 X5 models due to a loose steering column connection that may cause handling issues and crash risk. Owners must contact BMW for free inspection and repair.
BMWJan 29, 2021 - Lower riskMedical device
Confirm Biosciences Inc recalls Healgen COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) REF GCC)V-402a - Product Usage: is a lateral
Confirm Biosciences recalls Healgen COVID-19 IgG/IgM Rapid Test Cassette (REF GCC)V-402a due to distribution outside Emergency Use Authorization and inadequate validation for fingerstick home testing. Affected units include specific lot numbers.
Confirm BiosciencesJan 29, 2021 - Use cautionMedical device
Stryker Communications recalls S-Series Equipment Management System; Model Number(s):0682400550; UDI: 07613327400502 Components that are affected
Stryker recalls S-Series Equipment Management System models with capacitive touch controls that may disengage when electrocautery devices are used, posing a risk of equipment malfunction during medical procedures.
StrykerJan 29, 2021 - Use cautionMedical device
Getinge Group Logistics America, LLC recalls Anesthesia gas-machine - Product Usage: intended for use in administering anesthesia while controlling the entire
Getinge recalls Flow i anesthesia machines with FiCO2 value errors or system check failures. Affected models include Flow i C20, C30, C40 and Flow c systems with specific serial numbers. Users should contact Getinge for remedy.
GetingeJan 29, 2021 - Stop using nowMedical device
Draeger Medical, Inc. recalls ID Circuit Basic (N) 180-Drager Breathing Circuits/Anesthesia Sets Order Number: MP01327 - Product Usage: Breathing
Draeger Medical recalls ID Circuit Basic (N) 180 breathing circuits due to potential detachment causing ventilation leaks. All units are affected. Contact for replacement.
Draeger MedicalJan 29, 2021 - Use cautionDrug
Akebia Therapeutics dba Keryx Biopharmaceutials, Inc recalls Auryxia (ferric citrate) tablets, 210 mg*, 200 tablets bottle, RX ONLY, Manufactured for and distributed by: KERYX
Keryx Biopharmaceuticals recalls Auryxia tablets due to failed dissolution specifications. Check lot numbers CDKSN, CDPPH, and CDPPK for expiration dates in Jan/Feb 2022.
AuryxiaJan 29, 2021 - Use cautionFood
Renaissance Food Group, LLC recalls BUFFALO STYLE CHICKEN Sliders NET WT. 5OZ (141g) Ingredients: Tuna Salad*** CONTAINS: EGG, FISH (TUNA), MILK, WHEAT
Renaissance Food Group recalls Buffalo Style Chicken Sliders because the label fails to list soy, posing a risk to those with allergies.
Renaissance Food GroupJan 29, 2021 - Use cautionVehicle
AUTOCAR XPEDITOR (2021) recall — Seat Belts
Autocar recalls 2018-2021 Xpeditor vehicles with seat belt harness routing too close to seat mechanism. This could cause engine stalling without warning, increasing crash risk. Owners must contact Autocar for free repairs.
AutocarJan 28, 2021 - Use cautionVehicle
JEEP GLADIATOR (2020) recall — Power Train
Chrysler recalls 2020 Jeep Gladiator vehicles with manual transmissions due to overheated clutch components that may cause fire or debris falling onto roads, increasing crash risk.
JeepJan 28, 2021 - Lower riskMedical device
OriGen Biomedical, Inc. recalls Evolve Cell Culture Bags, part numbers: EV1000N and EV3000N The Evolve bag is made of Ethyl Vinyl Olefin (EVO) and
OriGen Biomedical recalls Evolve Cell Culture Bags (EV1000N, EV3000N) due to incorrect labeling as phthalate-free. These bags are made of EVO and contain no BPA or latex.
OriGen BiomedicalJan 28, 2021 - Lower riskMedical device
Biomerieux Inc recalls VITEK 2 Compact (version numbers 8.01, 8.02 (8.0x) and 9.01, 9.02 (9.0x) with the external communication configured to
Biomerieux recalls VITEK 2 Compact (versions 8.01-9.02) with HL7 configured external communication due to potential false susceptible test results. Lab technicians may need to manually correct LIS results, risking incorrect treatment decisions.
BiomerieuxJan 28, 2021 - Lower riskMedical device
Baxter Healthcare Corporation recalls Prismaflex Control Unit - Product Usage: Used for Continuous Renal Replacement Therapy (CRRT).
Baxter Healthcare recalls Prismaflex Control Units used for CRRT due to tubing variability causing alarm situations during self-tests. Affected units have specific serial numbers listed in the recall notice.
Baxter HealthcareJan 28, 2021 - Use cautionMedical device
Olympus Corporation of the Americas recalls Duodenoscope and accessories, flexible/rigid - Product Usage: used with an Olympus video system center, light source,
Olympus recalls TJF-Q190V duodenoscopes after reports of mucosal injuries from forceps elevator regions. Affected units include specific models used with Olympus video systems.
OlympusJan 28, 2021 - Lower riskDrug
Accord Healthcare, Inc. recalls Glycopyrrolate Injection, USP 0.4 mg/2 mL (0.2 mg/mL) 25 x 2 mL Single Dose Vials Rx Only, Manufactured for: Accord
Accord Healthcare recalls 25x2mL Glycopyrrolate injection vials due to label mix-up with 1mL vials. Correctly labeled vials were packaged into blister strips intended for 1mL vials.
Accord HealthcareJan 28, 2021 - Lower riskFood
Dole Fresh Vegetables Inc recalls Dole Endless Summer Salad Kit; 13 oz. bag UPC: 0-71430-01073-0 Contains Milk, Wheat Distributed by Dole Fresh
Dole recalls 13 oz. Endless Summer Salad Kits with undeclared fish and eggs in Caesar dressing. Consumers may check UPC 0-71430-01073-0 for affected items.
DoleJan 28, 2021
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