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
34,894 found- Stop using nowConsumer product
John Deere Recalls Compact Utility Tractors Due to Injury Hazard (Recall Alert)
John Deere recalls 1023E and 1025R compact utility tractors due to rollover protective structure (ROPS) that can loosen and fail during rollovers, risking operator injury.
John DeereDec 12, 2017 - Stop using nowConsumer product
Dream On Me Recalls Crib & Toddler Bed Mattresses Due to Violation of Federal Mattress Flammability Standard
Dream On Me recalls crib and toddler bed mattresses from 2016 that fail federal flammability standards. Consumers must stop using and get a free fire-resistant cover to prevent fire risks.
Dream On MeDec 12, 2017 - Lower riskMedical device
Philips Electronics North America Corporation recalls digital x-ray detector ProGrade R1 - solid state X ray imager (flat panel/digital imager) As a part of a radiographic
Philips recalls ProGrade R1 digital X-ray detectors with weak WiFi connections that may cause images to fail transferring to the system, requiring re-takes. Affected units have specific serial numbers.
PhilipsDec 11, 2017 - Lower riskMedical device
Philips Medical Systems (Cleveland) Inc recalls Ingenuity TF PET/CT (model 882442) running software version 4.0.2 This device is a diagnostic imaging system that
Philips recalls Ingenuity TF PET/CT (model 882442) software version 4.0.2 due to intermittent PET reconstruction failures causing unusable scans. Affected units may show error messages during reconstruction.
PhilipsDec 11, 2017 - Lower riskMedical device
Boston Scientific Corporation recalls Boston Scientific Guider Softip XF Guide Catheter Product Usage: Is a neurovascular access catheter that creates a
GUIDER
GUIDERDec 11, 2017 - Lower riskMedical device
Smith & Nephew, Inc. recalls Smith & Nephew Whipknot Soft Tissue Cinch #5 Sutures. PN: 7211015
Smith & Nephew recalls specific sutures due to packaging that may allow sterile barrier breaches. Affected batches include 7211015 with batch numbers 50498479-50603355. Stop using if you have these items.
Smith & NephewDec 11, 2017 - Lower riskMedical device
Medical Action Industries Inc recalls Medical Action Industries Inc. Blue OR Towel Non X-Ray Detectable (6 Towels per Pack) / product # AVID266 Sterile This
Medical Action Industries recalls sterile blue OR towels that may have compromised sterility. These hospital-grade towels are for blood and bodily fluid absorption. Affected items have specific lot numbers and expiration dates.
Medical Action IndustriesDec 11, 2017 - UnratedMedical device
Sanofi Genzyme recalls Synvisc-One ¿ (hylan G-F 20), 6mL delivered from a 10mL syringe Product Usage: A elastoviscous high molecular weight
Sanofi Genzyme recalls Synvisc-One (hylan G-F 20) due to contamination with Methylbacterium thiocyanatum. This injectable treatment for knee osteoarthritis may pose health risks if used.
Sanofi GenzymeDec 11, 2017 - Lower riskMedical device
Smith & Nephew, Inc. recalls smith&nephew Mini-Fragment Plating System, VLP(R) Mini-Mod Small Bone Plating System, EVOS(R) Mini Plating system,
Smith & Nephew recalls specific bone plate models due to incorrect labeling causing potential use of wrong plate size during surgery. Affected units include VLP MINI-MOD 2.0MM STRAIGHT PLATE 8 HOLE with a Stout plate.
Smith & NephewDec 11, 2017 - Lower riskFood
Lovejoy Bakers Inc recalls Rosemary Poppyseed crackers, net wt. 6 oz., packaged in clear poly bag with a twist tie. No UPC code. The label is read
Lovejoy Bakers recalls 6oz Rosemary Poppy: undeclared wheat in ingredients poses allergy risk. Check labels for wheat flour. No UPC code.
Lovejoy BakersDec 11, 2017 - Use cautionConsumer product
Ravin Crossbows Recalls Arrow Nocks Due to Injury Hazard
Ravin Crossbows recalls white plastic arrow nocks that can cause injury if not fully engaged with the bowstring, leading to potential discharge during re-nocking. Consumers should stop using and get free replacements.
Ravin CrossbowsDec 11, 2017 - Use cautionVehicle
VICTORY MAGNUM (2017) recall — Service Brakes, Hydraulic
Polaris recalls 2017 Victory Magnum motorcycles with a risk of brake line melting due to catalytic converter heat, potentially causing crashes. Owners must have brake line re-routed by dealers.
PolarisDec 10, 2017 - Use cautionVehicle
KEYSTONE RAPTOR (2018) recall — Suspension
Keystone is recalling 2018 Raptor toy haulers with faulty suspension equalizers that could fail during travel, increasing crash risk. Owners must contact customer service for free replacement.
KeystoneDec 10, 2017 - Use cautionVehicle
RAM 2500 (2017) recall — Engine And Engine Cooling
Chrysler is recalling 2013-2017 RAM 2500 trucks with leaking Concentric water pumps that could cause engine compartment fires. Owners must get free water pump replacements.
ChryslerDec 9, 2017 - Lower riskMedical device
Remel Inc recalls Remel Shigella sonnei Phase 1 & 2 Agglutinating Serum, Ref R30164201 ZH01. Product Usage: Suitable for the use in slide
Remel recalls Shigella sonnei Phase 1 & 2 Agglutinating Serum (Ref R30164201 ZH01) due to potential failure to agglutinate within specified time. Affected kits and bottles from specific lots are listed in the recall notice.
RemelDec 8, 2017 - Stop using nowMedical device
Hitachi Ltd., Medical System Operations Group recalls MHI-TM2000 Linear Accelerator System Product Usage: MHI-TM2000 Linear Accelerator System is intended for radiation
Hitachi recalls MHI-TM2000 Linear Accelerator Systems due to software issues that may cause incorrect patient radiation targeting during cancer treatment. Affected units have specific serial numbers.
HitachiDec 8, 2017 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Humeral Stem 83mm(Size 17) Product Usage: Intended for primary and revision total shoulder arthroplasty as well as
Zimmer Biomet recalls Humeral Stem 83mm (Size 17) due to incorrect lot numbers causing size mismatch. Affected patients should contact the manufacturer for guidance.
Zimmer BiometDec 8, 2017 - Lower riskMedical device
Abbott Laboratories, Inc recalls ARCHITECT c8000 Cuvette Segment, Part #01G46-01/01G06, a component to the ARCHITECT Clinical Chemistry system. There
Abbott recalls ARCHITECT c8000 Cuvette Segments (Part #01G46-01/01G06) that may cause falsely low test results. Affected units include 165 cuvettes per reaction carousel. Consumers should contact Abbott for details.
AbbottDec 8, 2017 - Lower riskMedical device
Datex-Ohmeda, Inc. recalls CARESCAPE R860 ventilators with software version 10SP05 Product Usage: The CARESCAPE R860 ventilator is designed to
Datex-Ohmeda Inc is a leading manufacturer of medical equipment, including ventilators, monitors, and patient care systems. Their products are designed to improve patient outcomes and healthcare delivery.
Datex-Ohmeda IncDec 8, 2017 - Use cautionMedical device
Heidelberg Engineering recalls Widefield OCT software feature for the Spectralis HRA+OCT and variants
Heidelberg Engineering recalls Spectralis HRA+OCT devices with Widefield OCT software feature until FDA 510(k) clearance is obtained. This software feature requires specific hardware and licensing.
Heidelberg EngineeringDec 8, 2017 - Lower riskFood
AMS LLC dba Gagne Foods recalls Sensations cinnamon roll UNCOOKED DOUGH 450g, UPC: 236821197
Gagne Foods recalls Sensations cinnamon roll uncooked dough (450g) due to undeclared pecans visible to consumers. Affected products contain pecans that may cause allergic reactions.
Gagne FoodsDec 8, 2017 - Use cautionConsumer product
One Stop Shop Recalls Children's Pajamas Due to Violation of Federal Flammability Standard: Sold Exclusively at Foreman Mills
One Stop Shop recalls children's pajamas that fail federal flammability standards, risking burn injuries. Consumers should stop using and get a refund.
One Stop ShopDec 8, 2017 - Lower riskMedical device
Zimmer Biomet, Inc. recalls 6.5mm x 125mm x 16mm Cannulated Screw, Item Number: 110009948 (UDI: (01)00887868111327 (17)270421 (10)120910) Product
Zimmer Biomet recalls 6.5mm x 125mm x 16mm Cannulated Screws due to incorrect labeling of a smaller screw size. This could lead to improper use in medical procedures.
Zimmer BiometDec 7, 2017 - Lower riskMedical device
Helena Laboratories, Corp. recalls Cascade Abrazo aPTT Test Card, Model 5722, For Export Only. The firm name on the label is Helena Laboratories,
Helena Laboratories recalls export-only Cascade Abrazo aPTT Test Card Model 5722 due to potential false negatives from shorter clot times. Affected units sold with lot 2-17-5722 expiring 2018-09-30.
Helena LaboratoriesDec 7, 2017 - Lower riskMedical device
Boston Scientific Corporation recalls PROPONENT SR Pacemaker
Boston Scientific recalls PROPONENT SR pacemakers (Model L200) due to intermittent over-sensing of Minute Ventilation sensor signals, which may cause improper heart rhythm management.
Boston ScientificDec 7, 2017 - Lower riskDrug
SCA Pharmaceuticals recalls Ephedrine sulfate 5 mg/mL in 0.9% Sodium Chloride 10 mL in Single Dose Syringe, Total Volume 10 mL, Rx only, SCA
SCA Pharmaceuticals recalls 10mL single-dose ephedrine sulfate syringes due to missing lot and expiration dates on labels. This affects prescription-only medications sold in the US.
SCA PharmaceuticalsDec 7, 2017 - Use cautionDrug
Johnson & Johnson recalls Neutrogena deep clean purifying whipped foam cleanser, (Salicylic Acid 0.5%), aerosolized product in a can, NET WT. 5
Johnson & Johnson recalls Neutrogena deep clean purifying whipped foam cleanser due to leakage from container valve. Products may leak propellant and product, causing potential skin irritation. Stop using affected items immediately.
NeutrogenaDec 7, 2017 - Stop using nowDrug
BotanicalNow recalls BodySlim Herbal Advanced technology & Strong formula capsules, 400 mg, 30-count bottle, Barcode: 9567153432481
BotanicalNow recalls BodySlim Herbal Advanced capsules due to undeclared sibutramine. Check your bottle barcode and expiration date for details.
BotanicalNowDec 7, 2017 - Lower riskFood
World Finer Foods, Inc. recalls Rapunzel Vegetable Bouillon ( no added salt ), 2.4 oz. net weight, in a thick paper sleeve containing 8 foil-wrapped
World Finer Foods recalls Rapunzel Vegetable Bouillon (no added salt) due to incorrect labeling showing sea salt in ingredients. Affected lots include 112075, 113390, 114805, 116205, 118230, 119631.
World Finer FoodsDec 7, 2017 - Lower riskFood
The Hain Celestial Group, Inc. - Worldwide HQ recalls BluePrint ORGANIC Beet Blast Vegetable & Fruit Drink 16 fl.oz.(473mL) USDA Organic. Keep Refrigerated.
Hain Celestial recalls BluePrint Organic Beet Blast Vegetable & Fruit Drink due to potential incorrect product labeling. Consumers should check labels and contact the company for details.
Hain CelestialDec 7, 2017
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