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
35,025 found- UnratedDrug
Sunstar Americas, Inc. recalls Paroex (Chlorhexidine Gluconate) Oral Rinse, USP 0.12%, Alcohol Free, Rx only, packaged in: a) 1 pint (473mL) NDC
Sunstar recalls Paroex oral rinse due to potential Burkholderia cepacia contamination from manufacturing issues. Affected lots were sold from Dec 2020 to Sep 2022. Consumers should check their product details and contact Sunstar for guidance.
SunstarDec 28, 2020 - Lower riskFood
Hill Pharma Inc recalls Pisiva Pea Protein 80% 20 kg (44 lbs) packaged in poly lined kraft paper bags.
Hill Pharma recalls Pisiva Pea Protein 80% 20kg bags due to possible salmonella Worthington contamination. Consumers should check lot numbers and contact Hill Pharma for details.
Hill PharmaDec 28, 2020 - Use cautionMedical device
Philips North America recalls PHILIPS Incisive Computed tomography X-ray system Incisive CT Software Upgrade from V4.5.1.41921 to
Philips recalls specific Incisive CT software versions due to risk of patient table moving during scans, potentially causing collisions with operators.
PhilipsDec 24, 2020 - Use cautionMedical device
Philips Ultrasound Inc recalls Philips EPIQ Diagnostic Ultrasound System, Models EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W,
Philips recalls EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx & EPIQ CVxi ultrasound systems due to risk of control panel arm assembly failure from missing or loose screws under pressure.
PhilipsDec 24, 2020 - Lower riskFood
Lipari Foods Operating Company, LLC. recalls Backroad Country Spicy Cajun Mix 9 oz (255g) plastic bag. Packed by Troyer Manufacturing Millersburg, OH 44654.
Lipari Foods recalls Backroad Country Spicy Cajun Mix (9oz) due to undeclared milk allergen. Consumers should check lot numbers M24501, M26902, M28201 for affected products.
Lipari FoodsDec 24, 2020 - Lower riskMeat & poultry
CLS Gourmet CL Saigon Food Company Recalls Meat Products Produced Without Benefit of Inspection
USDA recalls 128,841 pounds of meat products made without federal inspection. Consumers urged not to eat these items; throw away or return to store.
CLS Gourmet CL SaigonDec 23, 2020 - Use cautionVehicle
INTERNATIONAL HV (2020) recall — Engine And Engine Cooling
Navistar recalls 2020-2021 International HV vehicles with potential engine movement when parking brake is engaged, risking crashes. Owners must update ECM parameters for safety.
NavistarDec 23, 2020 - Use cautionVehicle
CHEVROLET BOLT EV (2020) recall — Seat Belts
General Motors recalls 2020 Chevrolet Bolt EVs with potentially unsafe seat belt bolts that could fail in crashes, increasing injury risk. Owners must have bolts replaced free by dealers.
ChevroletDec 23, 2020 - Lower riskMedical device
Becton Dickinson & Company recalls BD Hypodermic Syringe 10 ml, eccentric tip. Catalog (Ref No.) 305482
Becton Dickinson recalls 10ml eccentric tip syringes with open seals that could compromise sterility. Affected units have catalog number 305482 and expire May 2023. Consumers should check packaging for open seals.
Becton DickinsonDec 23, 2020 - Lower riskMedical device
Draegar Medical Systems, Inc. recalls Infinity Acute Care System (IACS) Monitoring Solution: The IACS is intended for multi-parameter, physiologic patient
Draegar Medical Systems recalls Infinity M540 patient monitors (model MS25510, MS25520, MS26372, revisions 24-29) that may randomly reboot causing temporary disconnection from patient monitoring. This could lead to interrupted care if the error repeats.
Draegar Medical SystemsDec 23, 2020 - Stop using nowMedical device
Biomet, Inc. recalls A.L.P.S. Clavicle Plating System, Plate, Fixation, Bone, Item Number 233500004 - Product Usage: indicated for fixation
Biomet recalls clavicle plating system item 233500004 due to cold welding risk during surgery. This may cause drill fracture. Affected units have specific lot numbers.
BiometDec 23, 2020 - UnratedMedical device
Tenderneeds Fertility LLC recalls At Home Semi-Flex/Rigid Insemination Device (SKU 644042787903)
Tenderneeds Fertility LLC recalls all At Home Semi-Flex/Rigid Insemination Devices (SKU 644042787903) due to distribution without proper marketing authorization. No remedy specified in official notice.
Tenderneeds FertilityDec 23, 2020 - Lower riskMedical device
Tenderneeds Fertility LLC recalls Deluxe IntraCervical Insemination (ICI) Kit (3), SKU 382903096046
Tenderneeds Fertility recalls Deluxe IntraCervical Insemination Kits sold before Dec 9, 2019 due to lack of proper marketing authorization. No action needed as the product is unapproved but not dangerous.
Tenderneeds FertilityDec 23, 2020 - Use cautionMedical device
Combat Medical Systems, LLC recalls Fresh Whole Blood Donor Set (P/N 80-801-D NSN 6515016640306) . Blood convenience kit. The Fresh Whole Blood Doner Set
Combat Medical Systems recalls Fresh Whole Blood Donor Sets with potential bent or disconnected needles. Affected lots include MFG2977 through MFG3857. Stop using if you have these kits.
Combat Medical SystemsDec 23, 2020 - Use cautionDrug
Fresenius Kabi USA, LLC recalls Ketorolac Tromethamine Injection, USP, 30 mg per mL, packaged in 1 mL Single Dose Vials (NDC 63323-162-00); 25 x 1 mL
Fresenius Kabi recalls Ketorolac injection vials due to particulate matter found in some samples. This may cause serious injury if injected. Check your vial's lot number and contact the company for details.
Fresenius KabiDec 23, 2020 - Stop using nowDrug
Genus Lifesciences Inc. recalls Oxycodone Hydrochloride Oral Solution, USP 5 mg/5mL unit dose cups, Rx Only, Genus Lifesciences Inc. NDC 64950-354-05
Genus Lifesciences recalls 5 mg/5mL oxycodone oral solution units with particulate matter. Affected lots have specific NDC and expiration dates. Stop using if you have these products.
Genus LifesciencesDec 23, 2020 - Stop using nowDrug
Shane Erickson Inc recalls IMC Wash-Free Hand Sanitizer, (ethyl alcohol), 75%, 1.7 fl. oz. (50 ml) bottles, Distributed by IMC 4284 Shoreline Dr,
IMC recalls 36,505 bottles of Wash-Free Hand Sanitizer due to CGMP deviations. The product may contain methanol and be subpotent for ethanol.
IMCDec 23, 2020 - Stop using nowFood
B & I Overseas Trading Inc. recalls Herring in Oil with Italian Spices: Ingredients: Herring fillet pieces (fish) sunflower oil refined deodorized, edible
B & I Overseas Trading recalls herring in oil with Italian spices due to Listeria monocytogenes contamination. Products sold in the US with UPC 40823097903896 from 2021.
B & I Overseas TradingDec 23, 2020 - Stop using nowConsumer product
Urban Outfitters Recalls Taper Candle Holders Due to Fire Hazard
Urban Outfitters recalls Swirled and Sofia Taper candle holders due to fire risk from candle flames. Affected items include amber, green, moss, lavender, and peach colors with specific SKU numbers. Return for full refund or prepaid label.
Urban OutfittersDec 23, 2020 - Use cautionConsumer product
King of Fans Recalls Hampton Bay Mara Ceiling Fans Due to Injury Hazard; Sold Exclusively at Home Depot
King of Fans recalls Hampton Bay Mara ceiling fans due to risk of blade detachment causing injury. Affected fans sold exclusively at Home Depot with specific UPCs. Consumers should stop using and inspect for blade movement or gaps.
King of FansDec 23, 2020 - Use cautionConsumer product
GSK Consumer Health Recalls Five Excedrin Brands Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning
GSK recalls Excedrin migraine and headache caplets with possible holes in the bottom that could allow children to access contents, risking poisoning. Check bottles for holes and contact for refunds if needed.
GSK Consumer HealthDec 23, 2020 - Use cautionVehicle
CHEVROLET BOLT EV (2020) recall — Service Brakes, Hydraulic
General Motors recalls 2020 Chevrolet Bolt EVs with potentially flawed front left brake calipers that could fracture during hard braking, risking reduced brake performance and crashes.
ChevroletDec 22, 2020 - Lower riskMedical device
Fujifilm Medical Systems U.S.A., Inc. recalls Wako HDL-C/LDL-C Calibrator - Product Usage: designed to be used with Wako L-Type HDL-C or L-Type LDL-C for the
Fujifilm recalls Wako HDL-C/LDL-C Calibrator (Lot EL62:9) due to incorrect concentration values on labels, which may lead to inaccurate cholesterol test results. Affected units should be checked for the specific lot number.
FujifilmDec 22, 2020 - Lower riskMedical device
EOS Imaging recalls The EOSedge system may acquire two simultaneous orthogonal planar images for a standing or seated patient at low dose.
EOS Imaging recalls specific EOSedge systems that may produce inaccurate images if patient is not positioned correctly during scans. Affected units can be identified by serial numbers listed in the recall notice.
EOS ImagingDec 22, 2020 - Lower riskMedical device
Cytocell Ltd. recalls Aquarius LPH 511-A CRLF2 Distal Probe Green, model no. LPH 511-A The CRLF2 Distal probe, labelled in green, consists of
Cytocell recalls Aquarius LPH 511-A CRLF2 Distal Probe Green due to potential false lab test results. This may cause normal samples to be incorrectly reported as abnormal in certain tests.
CytocellDec 22, 2020 - Lower riskMedical device
Abbott Point Of Care Inc. recalls Abbott i-STAT CG8+ cartridges - IVD Intended for quantitative measurement of sodium, potassium, ionized calcium,
Abbott recalls i-STAT CG8+ cartridges that may show higher than expected calcium results when stored at room temperature for more than 3 days (lots *20100-*20339) or 7 days (lots *20340+).
AbbottDec 22, 2020 - Lower riskDrug
Edge Pharma, LLC recalls Epinephrine/Lidocaine HCl, Sterile Ophthalmic Solution for Injection, 0.8 mL per syringe, Single Use Syringe,
Edge Pharma recalls sterile ophthalmic solution for injection with missing lot or expiration date. This affects prescription-only 0.8mL syringes sold in 2020. Contact for replacement.
Edge PharmaDec 22, 2020 - UnratedDrug
Strides Pharma Inc. recalls NDC 64380-721-06 TACROLIMUS CAPSULES, USP 1mg 100 Capsules Rx Only Manufactured by: Strides Pharma Science Ltd.
Strides Pharma recalls 1mg Tacrolimus capsules due to failed moisture limits. This may affect drug stability and safety. Consumers should contact the manufacturer for details.
Strides PharmaDec 22, 2020 - Lower riskFood
Gem City Fine Foods, LLC recalls Vegan Chocolate Cake, 25 oz., packaged in plastic base/cake dome, UPC 855026001421, Gem City Fine Foods,
Gem City Fine Foods recalls 25 oz. Vegan Chocolate Cake with mislabeled nutrition facts and ingredients. Products sold online with UPC 855026001421 may be affected. No remedy provided.
Gem City Fine FoodsDec 22, 2020 - Lower riskFood
American Blue Ribbon Holdings LLC recalls 9" French Silk Base, Item 7545, Count per case 6 Ea., Case Weight 12 lb. 3 oz. UPC 50796220075458. Keep Frozen.
American Blue Ribbon Holdings LLC recalls 9" French Silk Base (Item 7545) due to undeclared pecan in frozen product. Consumers should check for lot code CH20322CPS on pie tin.
American Blue RibbonDec 22, 2020
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