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
35,004 found- Lower riskMedical device
Qualigen Inc recalls The FastPack System Comlete Immunoassay Kit Immunoassay for the Quantitative Measurement of SHBG is a chemiluminescent
Qualigen recalls FastPack SHBG immunoassay kits due to potential inaccurate hormone binding globulin measurements. This may affect medical testing for hormone disorders.
QualigenNov 6, 2019 - Lower riskMedical device
The Binding Site Group, Ltd. recalls Rheumatoid Factor (RF) Kit for use on SPAPLUS, for in-vitro diagnostic use, Product code: LK151.S.A. , UDI:
The Binding Site Group recalls Rheumatoid Factor (RF) Kit for false positive test results due to calibrator values over recovering. Affected kits may cause unnecessary testing.
The Binding Site GroupNov 6, 2019 - Use cautionMedical device
Stryker Instruments Div. of Stryker Corporation recalls Color Cuff Disposable Tourniquet Cuff, 18 inch X 3 inch, 1BLA (Single Bladder), 2PRT(Dual Port) Quick Connect
Stryker recalls disposable tourniquet cuffs that may leak air, causing loss of blood flow during surgery. Affected units have specific model and lot numbers. Consumers should contact Stryker for details.
StrykerNov 6, 2019 - Lower riskMedical device
Allergan PLC recalls Natrelle Silicone Filled Breast Implants for the following Styles and Sizes: Style 10, Style 15, Style 20, Style 40,
Allergan, PLC. - Allergan
Allergan, PLC.Nov 6, 2019 - UnratedDrug
Golden State Medical Supply Inc. recalls GSMS: Ranitidine Capsules 150 mg, Rx only, 500 count bottles (NDC 51407-097-05) Manufactured by Novitium Pharma LLC, 70
Golden State Medical Supply recalls 150mg ranitidine capsules (Rx only) with NDMA impurity. Products manufactured by Novitium Pharma LLC, NDC 51407-097-05, may pose health risks.
Golden State Medical SupplyNov 6, 2019 - UnratedDrug
AuroMedics Pharma LLC recalls Ranitidine Syrup (Ranitidine Oral Solution, USP), 15 mg/mL (75 mg/5mL) 474 mL bottle, Rx only Distributed by: Aurobindo
AuroMedics Pharma LLC recalls Ranitidine Syrup (15 mg/mL) due to detected N-nitrosodimethylamine (NDMA) contamination. This chemical is a potential carcinogen. Consumers with this product should contact the manufacturer for guidance.
AuroMedicsNov 6, 2019 - Stop using nowFood
Amazon recalls Amazon Go Tzatziki Dip with Veggies, refrigerated. Net weight: 6.2 ounces. UPC: 8 42379 12607 9.
Amazon recalls refrigerated Tzatziki dip with veggies (6.2 oz) due to potential Listeria monocytogenes contamination. All units with Best By dates through November 6, 2019 are affected.
AmazonNov 6, 2019 - Use cautionConsumer product
Skacel Collection Recalls FlipStix Knitting Needles Due to Laceration Hazard
Skacel recalls US 6 FlipStix knitting needles due to risk of shaft splitting causing lacerations. Consumers should stop using and get a refund via store voucher.
SkacelNov 6, 2019 - Lower riskMedical device
Dako Denmark A/S recalls Dako Autostainer instruments: Autostainer Link 48, Model AS480; Autostainer Plus Link Instrument, Model AS100;
Dako recalls Autostainer Link 48 (AS480) and Plus Link (AS100) models with potential buffer leakage if syringe tray is missing. Updated guide reduces false negatives.
DakoNov 5, 2019 - Lower riskMedical device
King Systems Corp. dba Ambu, Inc. recalls King Vision Video Adapter Size 1/2. Laryngoscope used to examine and visualize a patients upper airway and aid in the
King Systems recalls specific laryngoscope video adapters due to reversed image display causing user actions to appear reversed left/right during airway exams.
King SystemsNov 5, 2019 - Lower riskMedical device
Collagen Matrix Inc recalls GIBSON Healthcare Membrane Extended, 20mm x 30mm, Reference Number 5303-324 - Product Usage: Indicated for use in oral
Collagen Matrix Inc recalls GIBSON Healthcare Membrane Extended (20mm x 30mm) for possible incorrect instructions. This oral surgical product may cause confusion in use. Consumers should check product details and contact the company for guidance.
Collagen MatrixNov 5, 2019 - Use cautionMedical device
Avanos Medical, Inc. recalls Haylard Closed Suction System for Neonates/Pediatrics, 5 Fr, 1. REF 195, Y-Adapter, SAP Finished Product Code
Avanos Medical recalls Haylard Closed Suction Systems for neonates/pediatrics with potential blocked catheters that may cause inadequate suction and oxygen desaturation. Affected units include specific model numbers and lot codes from 2022-2024.
Avanos MedicalNov 5, 2019 - Lower riskFood
Beatrice Bakery Co recalls Nut Bread Net Wt. 16 oz (454 g), Maufactured by Beatrice Bakery Co, Beatrice, NE.
Beatrice Bakery Co recalls 16 oz nut bread due to mold growth before best by date. Consumers should check for mold and discard if present.
Beatrice Bakery CoNov 5, 2019 - Stop using nowFood
Peekay International, Inc. recalls Dry dates packaged under the following brands: Keshav Dry Yellow Dates, 7oz., UPC: 643864233124 and 14oz., UPC:
Peekay International recalls Keshav and Swan brand dry yellow dates due to undeclared sulfites, which pose a risk to those with allergies. Check your UPCs.
Keshav / SwanNov 5, 2019 - UnratedFood
Hart Freeze Pack, LLC recalls 3/8" diced IQF zucchini in 45 pound poly lined carton
Hart Freeze Pack recalls 3/8" diced IQF zucchini in 45-pound poly lined cartons due to potential Listeria Monocytogenes contamination. Consumers should check product codes and take action if affected.
Hart Freeze PackNov 5, 2019 - Lower riskFood
Cain Food Industries, Inc recalls OXIBAKE YF packaged in 50 lb. Multi-wall paper bag with polyethylene liner
Cain Food Industries recalls OXIBAKE YF packaged in 50 lb. paper bags with polyethylene liners due to possible Salmonella contamination. Consumers should check lot numbers for affected products.
Cain Food IndustriesNov 5, 2019 - UnratedFood
RMJV, LP DBA Fresh Creative Foods recalls Broccoli Cheddar Pasta Salad Kit V 1/3.7625 LBS Distributed By: Russ Davis Wholesale Wadena, MN 56482 UPC 1345435840
Fresh Creative Foods recalls Broccoli Cheddar Pasta Salad Kit V due to potential Listeria monocytogenes contamination. Consumers should check UPCs and lot dates for affected items.
Fresh Creative FoodsNov 5, 2019 - Stop using nowFood
Russ Davis Wholesale, Inc. recalls Veggie Pizza Mix, 2.5 lbs, packaged with a small generic white label on a plastic bag for foodservice use. Contains
Russ Davis Wholesale recalls 2.5 lb Veggie Pizza Mix due to potential Listeria monocytogenes contamination. Check your sell-by date and UPC.
Russ Davis WholesaleNov 5, 2019 - Lower riskMeat & poultry
Padrino Foods, LLC Recalls Beef Tamales Products due to Mislabeling
USDA recalls 1,931 pounds of beef tamales from Padrino Foods due to mislabeling with pork. Consumers urged not to consume; products should be thrown away or returned.
Padrino FoodsNov 4, 2019 - Lower riskMeat & poultry
Cay Thi Queentrees Food USA Recalls Poultry Products Produced Without Benefit of Import Inspection
USDA FSIS recalls 43,848 pounds of poultry products imported from Vietnam without required import inspection. Consumers urged not to consume these products.
Cay Thi Queentrees Food USANov 4, 2019 - Use cautionVehicle
SUBARU LEGACY (2014) recall — Electrical System
Subaru is recalling 2014 Legacy vehicles with mechanical key ignition switches that may unexpectedly turn off the engine, increasing crash risk and airbag failure. Owners must have ignition switch inspected and replaced if needed.
SubaruNov 4, 2019 - Use cautionVehicle
DODGE DART (2016) recall — Power Train
Chrysler recalls 2016 Dodge Darts with 6-speed automatic transmissions due to shifter cable bushing failure that may cause vehicle to roll away or not shift properly, increasing crash risk. Owners must contact Chrysler for free transmission side shifter cable bushing replacement.
ChryslerNov 4, 2019 - Stop using nowVehicle
DYNAMAX ISATA (2018) recall — Power Train
Forest River recalls 2018 Dynamax Isata vehicles with column shift for unintended transmission shifts causing rollaway. Owners must contact for free software update and BTSI inspection.
Forest RiverNov 4, 2019 - Lower riskMedical device
Medacta Usa Inc recalls Medacta Shoulder SYSTEM HUMERAL ANATOMICAL METAPHYSIS, REF 04.01.0023 through 04.01.0055, all sizes - Product Usage:
Medacta recalls specific shoulder implant models (ref 04.01.0023-04.01.0055) due to potential screw insertion issues. Affected users should check their implant lot numbers.
MedactaNov 4, 2019 - Use cautionMedical device
Becton Dickinson & Company recalls Site~Rite 8 Ultrasound Systems-intended for diagnostic ultrasound imaging of the human body. Site~Rite 8 Ultrasound
Becton Dickinson recalls Site~Rite 8 Ultrasound Systems that may abruptly shut down without warning when running on battery power. This could cause interruptions in medical imaging.
Becton DickinsonNov 4, 2019 - Lower riskMedical device
Integra Lifesciences Sales Llc recalls Ascension¿ Silicone PIP-Silicone PIP Sz 1, Model Number: SPIP5201WW - Product Usage: The Ascension Silicone PIP implant
Integra Lifesciences recalls Ascension Silicone PIP implants mislabeled as size 1 when actually size 0. This labeling error may cause incorrect implant placement. Consumers should contact the manufacturer for details.
Integra LifesciencesNov 4, 2019 - Lower riskMedical device
Immuno-Mycologics, Inc recalls Histoplasma Immunodiffusion (ID) Antigen; The IFU labeling is for multiple products which included Fungal Antigens,
Immuno-Mycologics recalls specific Histoplasma Immunodiffusion antigen products due to potential false positive results from reagent contamination. Affected items include Lot L106909 with UDI # (01) 008163870:20391. No action needed if not affected.
Immuno-MycologicsNov 4, 2019 - Lower riskMedical device
Shimadzu Medical Systems recalls Trinias DAP Meter, a component of the Digital Anglo System Trinias contained within the DAR-9500f - Product Usage: It
Shimadzu recalls Trinias DAP meters (serials LR051A58B027-029) used in Digital Anglo System for medical procedures due to being outside tolerance. Affected users should contact Shimadzu for details.
Shimadzu Medical SystemsNov 4, 2019 - Use cautionMedical device
Villa Sistemi Medicali S.P.A. recalls Juno DRF, Model Number 709020 - Product Usage: General. multi-function x-ray systems capable of routine radiographs and
Villa Sistemi recalls Juno DRF model 709020 x-ray systems due to potential angulation chain failure after 8 years of use, risking metal fatigue under heavy workload.
Villa SistemiNov 4, 2019 - Lower riskMedical device
Trilliant Surgical, LLC recalls 8mm HTR Sterile Hammer Toe Reaming Kit, Material: Stainless Steel, Sterile: R, PX only, UDI:
Trilliant Surgical recalls 8mm HTR Sterile Hammer Toe Reaming Kit (lot TSL007202) due to potential incorrect reamer types. Affected kits may have two of the same reamer instead of one concave and one convex. Contact for remedy.
Trilliant SurgicalNov 4, 2019
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