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
35,021 found- Lower riskMedical device
Pentax of America Inc recalls 9372HD Digital Capture (ver. 1.1.0 + w/ 9263 endoPortal),
Pentax recalls 9372HD Digital Capture systems with version 1.1.0+ where exam videos could be copied between patients during follow-up reviews. Affected units have specific computer serial numbers listed.
PentaxSep 22, 2020 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls ADVIA Chemistry Systems-Fructosamine (FRUC)-For in vitro diagnostic use in the quantitative measurement of glycated
Siemens Healthcare recalls ADVIA Fructosamine test kits that may show 60 umol/L higher glucose levels than actual, risking incorrect diabetes treatment adjustments. Affected kits have specific Siemens Material Numbers.
Siemens HealthcareSep 22, 2020 - Stop using nowFood
Advanced Spice & Trading, Inc. recalls Ground Cinnamon 2% (CASSIA) packaged in 50 pound bag
Advanced Spice & Trading recalls 7,400 lbs of Ground Cinnamon due to potential Salmonella contamination. Check your lot numbers.
Advanced Spice & TradingSep 22, 2020 - Use cautionVehicle
GENESIS G70 (2021) recall — Fuel System, Gasoline
Hyundai recalls certain 2021 Genesis G70 vehicles with 2.0L GDI engines due to a potential fuel pump issue that could cause engine stalling and crash risk. Owners will receive free repairs.
HyundaiSep 21, 2020 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Siemens Artis one systems with a Display Port transceiver-Fluoroscopic X-Ray System Model: 10848600 - Product Usage: he
Siemens recalls Artis One systems with specific model numbers due to potential display monitor issues during X-ray procedures. Affected units may show no display, flickering, or incorrect resolution.
SiemensSep 21, 2020 - Lower riskMedical device
Smith & Nephew, Inc. recalls Genesis (GII) - Product Usage: designed for use in patients in primary and revision surgery, where the posterior
Smith & Nephew recalls Genesis (GII) surgical devices due to a design flaw in the anterior locking detail that may not meet specifications. Affected models include 71420966 with lot 18JY09702.
Smith & Neph: Inc.Sep 21, 2020 - Use cautionMedical device
Stereotaxis Inc recalls Niobe ES System, Models 001-006000-1 and 001-006100-1
Stereotaxis recalls Niobe ES System models 001-006000-1 and 001-006100-1 due to potential fire in the computer cabinet. Affected units have specific serial numbers listed in the recall notice.
StereotaxisSep 21, 2020 - UnratedMedical device
Conformis, Inc. recalls iTotal Hip Replacement System, Model number HAA-050-D020-020102 The Conformis Hip System includes standard hip
Conformis recalls iTotal Hip Replacement System model HAA-050-D02: Incorrect hip components in kits may lead to improper joint replacement. Affected units have serial numbers 0469255.
ConformisSep 21, 2020 - Lower riskMedical device
GE Healthcare, LLC recalls Revolution Apex, Revolution CT with Apex Edition, Model 5995000-5 - Product Usage: The system is intended for head,
GE Healthcare recalls Revolution Apex and Revolution CT with Apex Edition models 5995000-5 for potential smudge artifacts that could affect medical imaging accuracy.
GE HealthcareSep 21, 2020 - Use cautionMedical device
Stryker Neurovascular recalls Trevo XP ProVue Retriever, REF (Size): 90182 (4MM x 20MM); 90185 (4MM x 30MM); 90186 (6MM x 25MM). Procedure Pack REF:
Stryker recalls specific models of Trevo XP ProVue Retriever due to increased risk of stent retriever separation from core wire during procedures, potentially leaving devices in vasculature. Affected units include certain sizes and reference numbers.
StrykerSep 21, 2020 - UnratedMedical device
Synthes (USA) Products LLC recalls END RING 17MM X 22MM LATERAL OR ANTERIOR/5 DEG (TI) Product Number: 495.394 - Product Usage: is a vertebral body
Synthes recalls END RING 17mm x 22mm spinal implants due to incorrect labeling as a general medical device instead of specially controlled medical device. Affected units have specific product numbers and lot numbers.
SynthesSep 21, 2020 - Lower riskMedical device
Smith & Nephew, Inc. recalls 5.5MM Arthrogarde Hip Access Cannula
Smith & Nephew recalls 5.5MM Arthrogarde Hip Access Cannulas with faulty J Lock that may not lock correctly into irrigation extenders or arthroscopes during surgery.
Smith & Neph: Inc.Sep 21, 2020 - Lower riskFood
Wismettac Asian Foods, INC recalls Shirakiku brand Black Fungus (Kikurage); 5 lb. bag, 6 x 5 lb. bags per case Item # 60403; UPC 0 74410 60403 5
Wismettac Asian Foods recalls Shirakiku Black Fungus (Kikurage) bags due to Salmonella ssp. serogroup B contamination. Consumers should check product codes and follow safety steps.
WismettacSep 21, 2020 - Stop using nowFood
Renaissance Food Group LLC recalls Trader Joe's Southwest Style Sweet Potato Saut¿ Bowl NET WT. 21.05oz (1 LB 5.5 OZ) 610g UPC 00661126 packaged in a
Trader Joe's recalls Southwest Style Sweet Potato Sauté Bowls due to undeclared eggs and milk. Check your Best By dates and lot codes for details.
Trader Joe'sSep 20, 2020 - Lower riskFood
Dianne's Fine Desserts recalls Devonshire Bake Shop brand Lemon Italian Cream Cake, 10 , Yellow Cake Filled With Italian Lemon Cream, 12 slices
Dianne's Fine Desserts recalls Devonshire Bake Shop brand Lemon Italian Cream Cake due to undeclared peanuts. Consumers should check lot numbers for affected items.
Dianne's Fine DessertsSep 19, 2020 - Use cautionVehicle
NEWMAR VENTANA (2019) recall — Tires
Newmar recalls 2018-2019 Ventana motorhomes due to potential tire valve stem damage causing loss of pressure and crash risk. Owners should contact customer service for free repairs.
NewmarSep 18, 2020 - Use cautionVehicle
FOREST RIVER WILDWOOD (2020) recall — Trailer Hitches
Forest River recalls 2020 Wildwood trailers with faulty brake safety switches that may not activate during trailer separation, risking loss of vehicle control. Owners should contact customer service for free repairs.
Forest RiverSep 18, 2020 - Use cautionVehicle
BRAXTON CREEK BUSHWACKER (2020) recall — Structure
Braxton Creek is recalling 2020-2021 Bushwhacker 10FB and 10SS trailers due to lag bolts that may pull through the floor, risking trailer separation and crashes.
Braxton Creek RVSep 18, 2020 - Lower riskMedical device
Merete Medical GmbH recalls OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (tibia)
Merete Medical recalls OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails for tibia with mislabeling issues. Affected lots have specific use-by dates. Consumers should check their product labels.
Merete MedicalSep 18, 2020 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls ARTIS Icono Interventional Fluoroscopic X-Ray system - Product Usage: Intended Use: ARTIS is a family of dedicated
Siemens recalls ARTIS Icono Interventional Fluoroscopic X-Ray systems with software version VE20B due to a rare risk of incorrect catheter visualization during procedures, potentially endangering patients.
SiemensSep 18, 2020 - Use cautionVehicle
HONDA RIDGELINE (2020) recall — Equipment
Honda recalls 2017-2020 Ridgeline trucks with unsecured tonneau covers that may separate, causing road hazards and crashes. Owners must get free tethers installed by dealers.
HondaSep 17, 2020 - Use cautionVehicle
FOREST RIVER BERKSHIRE (2020) recall — Tires
Forest River recalls 2020 Berkshire motorhomes for potential tire valve stem damage that could cause loss of tire pressure, increasing crash risk. Owners should contact customer service for free inspection or replacement.
Forest RiverSep 17, 2020 - Lower riskMedical device
THREAD COUNSEL INC DBA LAWS OF MOTION recalls LOM Disposable Surgical Gowns/Medical Gowns, Single-Use
Laws of Motion recalls single-use disposable surgical gowns that lack proper labeling and may not meet FDA standards for surgical gowns. Affected lots 1-47.
Laws of MotionSep 17, 2020 - Lower riskMedical device
Quidel Corporation recalls Sofia SARS Antigen FIA Package Insert The Sofia SARS Antigen FIA is a lateral flow immunofluorescent sandwich assay
Quidel recalls Sofia SARS Antigen FIA tests that may give false positive results if viral transport media is used. Consumers should test directly from swabs without transport media.
QuidelSep 17, 2020 - Use cautionMedical device
Genicon, Inc. recalls A Li-Gator Single Use Laparoscopic Clip Applier, 10 mm X 29 cm - Product Usage: intended for use on tubular structures
Genicon recalls single-use laparoscopic clip appliers (model 360-010-001) due to jamming and clip loading failures. Affected units sold with specific lot codes.
GeniconSep 17, 2020 - Lower riskMedical device
GE Healthcare, LLC recalls Flow Sensor Service Part, Catalog 2089610-001-S
GE Healthcare recalls flow sensors from August 2020 with potential small punctures in tubes. Affected models include Aespire 7100/11, Aespire 7900, and others. Stop using if you have these parts.
GE HealthcareSep 17, 2020 - Lower riskMedical device
Getinge Group Logistics America, LLC recalls Servo-i Ventilator, Part No. 6487800, UDI Code 07325710000823 - Product Usage: intended for general and critical
Getinge recalls Servo-i Ventilators with specific serial numbers due to a potentially shorter nebulizer connector that may cause difficulty installing the Aeroneb Nebulizer module. Affected units can be identified by serial numbers listed in the recall notice.
GetingeSep 17, 2020 - Lower riskDrug
PD-Rx Pharmaceuticals, Inc. recalls Nature-Throid 1 GR (65 mg), Each Tablet Contains: Thyroid USP 1 GR (65 mg), Liothyronine (T3) 9 mcg, Levothyroxine (T4)
PD-Rx Pharmaceuticals recalls Nature-Throid 1 GR (65 mg) tablets due to manufacturing deviations causing potential sub-potent levels. Affected products were repackaged under the same conditions as sub-potent products. No specific remedy is listed in the recall notice.
PD-Rx PharmaceuticalsSep 17, 2020 - Lower riskDrug
Acella Pharmaceuticals, LLC recalls NP Thyroid 15,Thyroid Tablets, USP 1/4 grain (15 mg) 100-count bottles, Rx Only, Manufactured For: Acella
Acella Pharmaceuticals recalls 100-count NP Thyroid 15 tablets (15 mg) due to subpotent levothyroxine content. FDA analysis shows these products contain less active ingredient than labeled, potentially causing inadequate thyroid hormone levels.
AcellaSep 17, 2020 - UnratedDrug
Grato Holdings, Inc. recalls Homeopathic Energy Catalyst, 1 fl oz (30 mL) Distributed by: Deseret Biologicals, Inc. 469 W. Parkland Drive Sandy, UT
Grato Holdings recalls Homeopathic Energy Catalyst 1 fl oz (30 mL) due to undeclared active ingredients and incorrect formulation. Consumers should check product labels for lot numbers Z60852 or Z60012.
Grato HoldingsSep 17, 2020
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