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
35,006 found- Use cautionVehicle
NISSAN LEAF (2020) recall — Back Over Prevention
Nissan is recalling 2020 LEAF electric vehicles where back-up camera images can disappear while reversing, failing to meet federal safety standards. Owners will receive free software updates.
NissanJul 17, 2020 - Stop using nowVehicle
LINCOLN NAUTILUS (2020) recall — Seats
Ford recalls certain Lincoln Nautilus vehicles due to seat cushion frames potentially damaging airbag wiring. Dealers will repair the harness free of charge.
LincolnJul 17, 2020 - Use cautionVehicle
FORD ESCAPE (2020) recall — Air Bags
Ford is recalling 2020 Escape vehicles with improperly crimped side curtain air bag diffusers that may detach during deployment, increasing injury risk. Owners must have the air bag modules replaced free of charge.
FordJul 17, 2020 - Lower riskMedical device
Materialise N.V. recalls Match Point System The Match Point System is intended to by uses as a surgical instrument to assist in the
Materialise recalls Match Point System surgical instruments due to incorrect procedure side labeling in Shoulder Case Planning Reports, which could lead to surgical errors.
MaterialiseJul 17, 2020 - Lower riskMedical device
Cytocell Ltd. recalls Cytocell LPH533-A NUP98 Distal Probe Green - Product Usage:The NUP98 Distal probe, labelled in green, consists of a
Cytocell recalls LPH533-A NUP98 Distal Probe Green due to potential false positive results with certain lab tests. This low-risk issue affects specific lot numbers.
CytocellJul 17, 2020 - Lower riskMedical device
Ortho Clinical Diagnostics recalls VITROS Anti-SARS-CoV-2 IgG Reagent Pack, COV2IgG, VITROS CoV2G. Catalog number 6199919, UDI 10758750033355 - Product
Ortho Clinical Diagnostics recalls VITROS Anti-SARS-CoV-2 IgG Reagent Packs due to potential false negatives or delayed results from swapped bottles. Affected lots 0010-0013.
Ortho Clinical DiagnosticsJul 17, 2020 - Lower riskMedical device
Medtronic Neuromodulation recalls Restore Clinician Programmer Application Software, model number A71100, used with the Restore Neurostimulators.
Medtronic recalls version 1.0.4232 of the Restore Clinician Programmer Application Software (model A71100) due to compatibility issues with some legacy software, preventing communication with implanted neurostimulators.
Medtr: a short, human brand name for headings (e.g. "Trsmima")Jul 17, 2020 - Lower riskMedical device
Diasorin Inc. recalls Parvovirus B19 IgG EIA kit Part No. V519IGUS
Diasorin recalls Parvovirus B19 IgG EIA kit (Part No. V519IGUS) due to incorrect label value. This may affect test accuracy. No remedy specified in recall notice.
Diasor:inJul 17, 2020 - UnratedMedical device
Ion Beam Applications S.A. recalls Proteus 235 The Proton Therapy System - Proteus 235 (brand names: Proteus Plus and Proteus ONE) is a medical device
Ion Beam Applications S.A. recalls Proteus 235 proton therapy systems due to inability to load treatment plans after abortion. Affected units have specific serial numbers from May 2019 (US) and October 2019 (EU).
Ion Beam Applications S.A.Jul 17, 2020 - Lower riskDrug
Lupin Pharmaceuticals Inc. recalls Lisinopril Tablets USP, 10 mg, 1000 count bottles, Manufactured by: Lupin Limited, Nagpur INDIA, For BluePoint
Lupin Pharmaceuticals recalls 10mg Lisinopril tablets due to foreign 20mg tablets in some bottles. Affected lots may contain unsafe medication.
Lupin PharmaceuticalsJul 17, 2020 - Lower riskFood
Giant Eagle recalls Giant Eagle Dried Island Fruit Mix , Net Wt. 10 oz. , 6 units per case. Packaging is a gusseted plastic resealable bag.
Giant Eagle recalls 10oz dried island fruit mix (expiring Jan 2021) due to potential undeclared peanut, almond, milk, and soy allergens. Consumers should check packaging for recall details.
Giant EagleJul 17, 2020 - Lower riskMedical device
Smith & Nephew, Inc. recalls Tibial knee prosthesis
Smith & Nephew recalls specific lots of Tibial knee prosthesis models due to potential internal material defects that could affect safety. Affected units include model numbers 71420164, 71420166, 71420184 and listed lot numbers.
Smith & NephewJul 16, 2020 - Lower riskMedical device
Oxford Immunotec recalls Model No:T-SPOT.TB8, Catalogue No.: TB.300; UDI: 1505171600030 - Product Usage: intended for use as an aid in the
Oxford Immunotec recalls T-SPOT.TB8 TB test kits with incorrect expiration dates on labels or substrate components. Affected kits may not be reliable for tuberculosis diagnosis.
Oxford ImmunotecJul 16, 2020 - Use cautionMedical device
Philips North America, LLC recalls Philips HeartStart MRx, Monitor/Defibrillators with model numbers M3535A, M3536A, M3536M, M3536MC, M3536M2, M3536M3,
Philips recalls HeartStart MRx defibrillators (models M3535A-M3536M9) due to potential therapy switch failure causing delayed or failed shocks. Affected devices may not deliver intended therapy during cardiac emergencies.
PhilipsJul 16, 2020 - Use cautionMedical device
Shanghai United Imaging Healthcare Co., Ltd. recalls uEXPLORER PET/CT Diagnostic Imaging System - Product Usage: This system is intended to be operated by qualified
Shanghai United Imaging Healthcare recalls uEXPLORER PET/CT scanners that may cause image artifacts and scanning interruptions due to signal drift. Affected units have serial numbers starting with F00002.
Shanghai United Imaging HealthcareJul 16, 2020 - Use cautionMedical device
Brainlab AG recalls BRAINLAB Kick 2; Model/catalogue (article) numbers for Kick: 18170; 18070 UDI (GTIN) for Kick: 04056481006655
Brainlab recalls Kick 2 navigation stations with incorrect calibration that may cause inaccurate measurements during surgery. Affected units have specific model and serial numbers listed in the recall notice.
BrainlabJul 16, 2020 - UnratedDrug
Grato Holdings, Inc. recalls HGH Vitality Homeopathic, 90 tablets, NDC 43742-1299-1, Dist. by Deseret Biologicals, Inc. 469 W. Parkland Drive,
Grato Holdings recalls HGH Vitality Homeopathic tablets due to a labeling error regarding the declared strength. Check your bottle's lot number.
HGH VitalityJul 16, 2020 - Lower riskFood
Greenhead Lobster Products recalls 1. FRESH CLAW AND KNUCKLE MEAT, 1 and 2 lbs. 2. FRESH CLAW, KNUCKLE, AND TAIL MEAT, 1 and 2 lbs 3. FROZEN CLAW AND
Greenhead Lobster Products recalls fresh and frozen lobster meat products that may be contaminated with Listeria monocytogenes. Consumers should check product dates and lot codes to determine if affected.
Greenhead Lobster ProductsJul 16, 2020 - Lower riskFood
Provident Nutraceutical div. of Ortho Molecular Products Inc recalls Dietary supplements, 60 capsules, UPC 15033-61832, Product # 832060, labeled under the following brands and product
Ortho Molecular recalls dietary supplements with UPC 15033-61832 that may contain undeclared soy. Consumers should check product labels for affected brands and contact the manufacturer for details.
Ortho MolecularJul 16, 2020 - Lower riskFood
J F C International Inc recalls Kasugai brand Matcha Ame (Green tea candy); 4.58 oz. plastic bag; 2 x 12 individual items per case Product of Japan
J F C International recalls Kasugai brand green tea candy due to undeclared soybean in mold lubricant. Check product details to determine if affected.
Kasug: the brand name from the titleJul 16, 2020 - Stop using nowConsumer product
Rocky Mountain Bicycles Recalls Non-Electric Instinct, Instinct BC and Pipeline Bicycles with Alloy Frames Due to Fall and Injury Hazards
Rocky Mountain recalls 2018-2020 Instinct, Instinct BC and Pipeline trail bikes with alloy frames due to risk of front frame cracking and falls. Affected models have serial numbers starting with PRK17, PRK18 or PRK19.
Rocky MountainJul 16, 2020 - Stop using nowConsumer product
Polaris Recalls Snowmobiles Due to Fire Hazard (Recall Alert)
Polaris recalls 2015-2020 AXYS Trail Performance and Crossover snowmobiles due to fire risk from improperly secured fuel hoses. Owners must stop using and contact a dealer for free repair or inspection.
PolarisJul 16, 2020 - Use cautionVehicle
BLUE BIRD ALL AMERICAN (2019) recall — Seat Belts
Blue Bird is recalling 2019-2021 All American buses with seat belts that may not stay anchored during crashes, risking injury. Owners should contact Blue Bird for free inspection and repair.
Blue BirdJul 15, 2020 - Use cautionVehicle
BLUE BIRD ALL AMERICAN (2019) recall — Seat Belts
Blue Bird is recalling 2019 All American school buses with seat belts that may not stay anchored in crashes, risking injury. Owners must have seat belt hardware inspected by dealers by August 2020.
Blue BirdJul 15, 2020 - Use cautionVehicle
TOYOTA TUNDRA (2020) recall — Exterior Lighting
Toyota recalls 2020 Tundra vehicles with faulty turn signals that may not flash brightly enough, increasing crash risk. Owners must have wire harness modified free by dealers.
ToyotaJul 15, 2020 - Lower riskMedical device
OraSure Technologies, Inc. recalls Pointts sistema de ellmlnact!;o de verrugas OTC - Brazil Catalog Number: 1001-0280 - Product Usage: indicated for
OraSure recalls Brazil-cataloged Pointts skin tag cryosurgical system (lot 9214, 9256) due to unsealed unit boxes. Consumers should check for unsealed packaging before use.
OraSureJul 15, 2020 - Lower riskMedical device
Medtronic Inc. recalls The Guardian Connect App CSS7200 iOS - Product Usage: intended for use by patients with a compatible consumer mobile
Medtronic recalls iOS app CSS7200 for patients with diabetes that stops automatically uploading glucose data to CareLink Personal website after software update.
MedtronicJul 15, 2020 - Use cautionMedical device
NeuroLogica Corporation recalls OmniTom Computed tomography x-ray system, Model NL5000, all NL5000 systems with software version before 05.01.01 -
NeuroLogica recalls all OmniTom NL5000 CT scanners with software version before 05.01.01 due to potential transport issues and system shutdowns that could delay patient treatment.
NeuroLogicaJul 15, 2020 - Lower riskMedical device
Qiagen Sciences LLC recalls QIAstat-Dx Respiratory SARS-CoV-2 Panel REF 691223 (US IVD under FDA EUA) - Product Usage: intended for the qualitative
Qiagen recalls QIAstat-Dx Respiratory SARS-CoV-2 Panel REF 691223 due to increased false positives for Influenza A, risking incorrect treatment and delayed diagnosis. Affected units include specific lots.
QiagenJul 15, 2020 - Lower riskMedical device
SICAT GMBH & CO. KG recalls SICAT IMPLANT V2.0
SICAT recalls IMPLANT V2.0 software due to incorrect export of implant positions in CMG.DXD format, potentially causing planning errors during dental procedures.
SICATJul 15, 2020
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