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- Lower riskMedical device
Integra LifeSciences Corp. recalls CODMAN HAKIM BACTISEAL Shunt System Clear with Barium Stripe Peritoneal Catheter 120cm, with drainage Holes and
Integra LifeSciences recalls CODMAN HAK: BACTISEAL shunt systems with incorrect labeling that may affect peritoneal catheter function. Learn if your device is affected and what to do.
Integra LifeSciencesMar 17, 2021 - Lower riskMedical device
Becton Dickinson & Co. recalls BD BBL Martin-Lewis Agar, 100 Ea - Product Usage: used for the isolation of pathogenic Neisseria from specimens
Becton Dickinson recalls BD BBL Martin-Lewis Agar due to heavy C. albicans growth after 24 hours, risking delayed Neisseria diagnosis. Affected lots: 0317559 (exp 2021-03-11) and 0345695 (exp 2021-04-06).
Becton DickinsonMar 17, 2021 - Lower riskMedical device
Medtronic Sofamor Danek USA, Inc recalls Endoskeleton TC Interbody System with Titan nanoLOCK Surface Technology, 6 Degree, Large, 8 mm, Product Number
Medtronic recalls Endoskeleton TC Interbody System with Titan nanoLOCK Surface Technology due to shelf box mislabeling. This may cause confusion about device size. No immediate action needed.
Medtr: a short, human brand name for headings (e.g.Mar 17, 2021 - Lower riskMedical device
CHANGE HEALTHCARE CANADA COMPANY recalls Change Healthcare Enterprise Viewer
Change Healthcare recalls Enterprise Viewer software versions 2.0 and 2:1 due to a software defect that may cause anchor study failures. Affected users should contact the company for updates.
Change HealthcareMar 17, 2021 - Lower riskDrug
Alembic Pharmaceuticals Limited recalls Telmisartan Tablets, USP 20 mg, 30-count bottles, Rx only, Manufactured by: Alembic Pharmaceuticals Limited
Alembic Pharmaceuticals recalls 20mg Telmisartan tablets due to label mixup. This medication is prescription-only and may be confused with other products. Consumers should contact the manufacturer for details.
Alembic PharmaceuticalsMar 17, 2021 - Lower riskFood
Power Selles Imports dba Culinary Collective recalls Blanxart Milk Chocolate with Hazelnuts Cacao 33% Min. Net wt.7 oz. Product is packaged with paper and internal foil
Culinary Collective recalls Blan: 7oz Blanxart Milk Chocolate with Hazelnuts Cacao 33% Min. containing a 0.5-inch metal fragment. Stop using immediately to avoid potential injury.
Culinary CollectiveMar 17, 2021 - Stop using nowFood
Real Water, Inc. recalls Real Alkalized Water, concentrate. 4 oz. glass bottle . Drinkrealwater.com
Real Water Inc. recalls alkalized water concentrate due to FDA-reported acute liver failure cases after consumption. Consumers should stop using affected products immediately.
Real WaterMar 17, 2021 - Stop using nowConsumer product

HOFISH Recalls Mattresses Due to Violation of Federal Flammability Standard; Sold Exclusively on Amazon.com
HOFISH recalls 10-inch hybrid mattresses sold on Amazon for failing federal flammability standards. Consumers must stop using and get a free fitted cover to comply with safety regulations.
HOFISHMar 17, 2021 - Stop using nowConsumer product

Global Home Imports Recalls Platform Bed Frames Due to Serious Injury Hazard
Global Home Imports recalls HR Platform bed frames (models HR33, HR33XL, HR46, HR50, HR60, HR6: Twin, Twin xl, Full, Queen, King, Cal King) due to collapse risk causing crush injuries or death. Consumers must stop using and get a free repair kit.
Global Home ImportsMar 17, 2021 - Use cautionVehicle
KEYSTONE COUGAR (2021) recall — Electrical System
Keystone is recalling 2021 Cougar RVs with Off the Grid Solar package due to potential electrical shock from energized shore power connections. Owners must contact customer service for free inverter testing and rewiring.
KeystoneMar 16, 2021 - Lower riskMedical device
Medtronic Inc. recalls Medtronic Abre Venous Self-expanding Sent System, Catalog number REF AB9U16080090 - Product Usage: intended for use in
Medtronic recalls Abre Venous Self-expanding System due to incorrect size printed on device, packaging labeled correctly. Affected units may have size mismatch risks.
MedtronicMar 16, 2021 - Lower riskMedical device
Boston Scientific Corporation recalls EXALT Controller - Product Usage: intended for use with a Boston Scientific endoscope for endoscopic diagnosis,
Boston Scientific recalls EXALT Controller devices with potential darker image settings for endoscopic procedures. Affected units have specific serial numbers and were sold with endoscopes for diagnosis.
Boston ScientificMar 16, 2021 - Use cautionMedical device
K2M, Inc recalls Chesapeake Cervical-Ti 10mm Drill Guide Inserter- a multi-screw construct providing stability to the anterior column
K2M recalls Chesapeake Cervical-Ti 10mm Drill Guide Inserter due to risk of spinal cord injury from improper implant seating. Affected units have catalog number 3608-90033 and lot number MNAJ.
K2MMar 16, 2021 - Lower riskMedical device
Biomerieux Inc recalls VIDAS¿ CMV IgM 30 Tests
Biomerieux recalls VIDAS CMV IgM 30 Tests with calibration issues in specific lots. Affected units may give inaccurate results; stop using and contact for replacement.
BiomerieuxMar 16, 2021 - Lower riskMedical device
Cardinal Health Inc. recalls OPTICHAMBER DIAMOND SPACER WITH LARGE MASK Item Number: 4742326
Cardinal Health recalls Diamond Spacer with Large Mask (Item 4742326) due to temperature exposure during shipping, which may cause inaccurate results. Affected units shipped between Feb 23, 2021 and March 10, 2021.
Cardinal HealthMar 16, 2021 - Lower riskMedical device
ICU Medical, Inc. recalls REF CL3946 Oncology Kit w/5" (13 cm) Add-On Set w/ChemoLock Additive Port, Vented Cap; ChemoLock , Spinning Spiros
ICU Medical recalls specific oncology kits due to potential leakage in certain lots of Sprios male luer fittings. This could lead to fluid leakage during patient administration. Affected kits have lot number 5142959.
ICU MedicalMar 16, 2021 - Lower riskFood
Bonduelle USA Inc. recalls El Sembrador Peas and Carrots, poly bags, 12/16 oz
Bonduelle USA recalls 12/16 oz El Sembrador Peas and Carrots bags due to possible blue plastic foreign object. Consumers should check product codes and contact for details.
Bondu:elMar 16, 2021 - Use cautionVehicle
BMW M440I (2021) recall — Air Bags
BMW recalls 2021 M440i convertibles due to potential head-thorax air bag failure in side crashes. Affected vehicles need software update from dealers.
BMWMar 15, 2021 - Lower riskMedical device
B. Braun Medical, Inc. recalls Filtered Triple-Leg Extension Set - Intravascular administration set. Product Catalog number: 477034 - Product Usage:
B. Braun recalls Filtered Triple-Leg Extension Set (catalog 477034) due to potential occlusion or inability to prime. Affected lots: 00SL713784, 0061741483, 0061755034, 0061755296.
B. BraunMar 15, 2021 - Use cautionMedical device
Medtronic Minimed recalls MiniMed 670G Insulin Pump: Models: PUMP MMT-1740KX 670G V6.3 SF MG CLIN;¿ PUMP MMT-1740KX 670G V6.3 CLIN 020 MG;¿ PUMP
Medtronic MiniMed recalls specific 670G insulin pump models due to a software issue that may cause insulin over-delivery if a user adds an additional bolus after a large insulin delivery. Affected models include PUMP MMT-1740KX 670G V6.3 SF MG CLIN and others with serial numbers listed.
Medtronic MiniMedMar 15, 2021 - Lower riskMedical device
Medline Industries Inc recalls Diluent, Stat-Site B-HB, 6x 3ML - Product Usage: Intended to be used with the Stat-Site test strips or KetoSite test
Medline recalls Diluent products that may cause false negative or positive test results due to shipment damage. Affected lots include 163878, 192821, 191991, 160795. Consumers should check their lot numbers.
MedlineMar 15, 2021 - Lower riskMedical device
St. Jude Medical, Cardian Rhythm Management Division recalls ENDURITY Pulse Generator REF PM**** SN ********* St. Jude Medical Cardiac Rhythm Assurity and Endurity pacemakers are
St. Jude Medical is a leading manufacturer of cardiac rhythm management products, including pacemakers, defibrillators, and other cardiac devices.
St. Jude MedicalMar 15, 2021 - UnratedDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Ganirelix Acetate Injection, 250 mcg/0.5 mL, Sterile Prefilled Syringe, Rx only, Distributor: Ferring Pharmaceuticals,
Sun Pharmaceutical recalls Ganire: 250 mcg/0.5 mL sterile prefilled syringes with failed impurities/degradation specs. Rx only. Check NDC 55566-1000-1 and lot numbers JKU1212A-JKU3314A.
Sun PharmaceuticalMar 15, 2021 - Lower riskDrug
Cardinal Health Inc. recalls Edarbi (azilsartan medoxomil) tablets 80 mg 30 Tablets Rx Only NDC 60631-080-30 Manufactured for: arbor Pharmaceuticals
Cardinal Health recalls Edar: 80mg tablets due to potential temperature exposure during storage. This may affect drug stability. Check NDC 60631-080-30 for affected units.
Cardinal HealthMar 15, 2021 - Lower riskFood
The Toasted Oat recalls The Toasted Oat Bakehouse Macadamia Chunk Soft Granola (6 - 10oz pouches per case); and Soft Granola Crumble Bars
Toasted Oat recalls Macadamia Chunk Soft Granola pouches and crumble bars with mold risk. Products sold between 2021-10-24 and 2021-12-03 may be affected. Check batch numbers for details.
The Toasted OatMar 15, 2021 - Lower riskFood
Nuts.com recalls Nuts.com brand Diced Dried Figs packaged in 1lb stand up gusset pouches.
Nuts.com recalls diced dried figs pouches containing undeclared almonds. Consumers should check product codes and stop using if they have these items.
Nuts.comMar 15, 2021 - Use cautionMeat & poultry
FSIS Issues Public Health Alert for Chicken Soup Product Due to Misbranding
FSIS public health alert: Albertsons chicken noodle soup labeled gluten-free but contains wheat. Consumers with gluten allergies should not eat these products, which are no longer available.
Albertsons CompaniesMar 12, 2021 - Stop using nowFood
Lehi Valley Trading Co, Inc recalls Buc-ee's Butter Toffee Almonds, 12 oz., packaged in clear zip top bag with stickered label, UPC: 0 9524842002 4,
Buc-ee's is recalling 12 oz. Butter Toffee Almonds because they are mislabeled and may contain peanuts, posing a risk to those with allergies.
Buc-ee'sMar 12, 2021 - Use cautionVehicle
VOLKSWAGEN TIGUAN (2022) recall — Service Brakes, Hydraulic
Volkswagen recalls 2022 Tiguan vehicles with loose brake pipe nuts that may cause brake fluid leaks and longer stopping distances, increasing crash risk. Owners can get free brake inspections.
VolkswagenMar 11, 2021 - Use cautionVehicle
VOLKSWAGEN ID.4 (2021) recall — Steering
Volkswagen recalls one 2021 ID.4 vehicle due to potential steering control loss from an incorrectly assembled or missing drive bushing. Owners must have their steering gear replaced at a dealer.
VolkswagenMar 11, 2021
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