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- Lower riskFood
Bell Plantation Inc. recalls Ready-to-Eat Powdered Peanut Butter in 1 lb (16 oz.) plastic jars
Bell Plantation recalls 16 oz. powdered peanut butter jars with E. coli levels exceeding safety standards. Consumers should check lot codes and contact the company for details.
Bell PlantationJan 24, 2018 - Stop using nowFood
Panera, LLC recalls Panera Reduced-Fat Plain Cream Cheese, 2 oz. and 8 oz.
Panera recalls reduced-fat plain cream cheese due to potential Listeria monocytogenes contamination. Consumers should avoid products with the listed lot numbers.
PaneraJan 24, 2018 - Stop using nowConsumer product
Fashion Accessory Bazaar Recalls Fidget Spinner Keychains Due to Choking Hazard
Fashion Accessory Bazaar recalls Pokemon-themed fidget spinner keychains due to choking hazard from loose center posts. Consumers must stop using and get refunds.
Fashion Accessory BazaarJan 24, 2018 - Use cautionMeat & poultry
Perdue Foods LLC Recalls Chicken Products due to Misbranding and Undeclared Allergens
Perdue Foods recalls chicken fritters containing undeclared egg allergens. Consumers should stop using these products immediately to avoid potential allergic reactions.
PerdueJan 23, 2018 - Lower riskMedical device
Biomerieux Inc recalls bioM¿rieux VITEK 2 NH ID Test Kit Product Usage: Is an automated system consisting of instruments, software and reagent
Biomerieux recalls VITEK 2 NH ID Test Kit due to missing desiccant, which may cause reagent degradation. Affected units have batch 2450570: 245057043, expired June 19, 2019.
BiomerieuxJan 23, 2018 - Use cautionMedical device
3M Company - Health Care Business recalls 3M Bair Hugger(M) Normothermia System, Full Access Underbody Warming Blanket, REF 63500 The 3M Bair Hugger Temperature
3M recalls specific models of Bair Hugger warming blankets due to potential airflow issues causing limited inflation. Affected units include lot numbers R10359-R10366. Contact 3M for details.
3MJan 23, 2018 - Lower riskMedical device
Implant Direct Sybron Manufacturing, LLC recalls Implant Direct, INTERACTIVE HEALING COLLAR, PART NUMBER 6530-15, 5.0mmL: 3.0mmD Platform
Implant Direct recalls a specific Interactive Healing Collar model due to improper sterilization before labeling as sterile. Affected units may pose infection risks if used.
Implant DirectJan 23, 2018 - Stop using nowFood
Bulletproof 360 Inc recalls Bulletproof Unflavored Collagen Protein High Performance Building Blocks Dietary Supplement, packaged in a 16-oz.
Bulletproof recalls unflavored collagen protein due to undeclared milk. People with milk allergies face serious risks from this mislabeled supplement.
BulletproofJan 23, 2018 - Use cautionVehicle
SUZUKI GSX-R1000 (2018) recall — Engine And Engine Cooling
Suzuki recalls 2017-2018 GSX-R1000 models due to potential drive chain breakage causing power loss and crash risk. Free replacement of engine control module and drive chain.
SuzukiJan 22, 2018 - Use cautionVehicle
FOREST RIVER CHEROKEE (2018) recall — Exterior Lighting
Forest River recalls 2018 Cherokee trailers with amber side marker lights too far back or missing reflectors, risking crashes. Owners get free fixes.
Forest RiverJan 22, 2018 - Use cautionMedical device
DeRoyal Industries Inc recalls Custom sterile surgical packs labeled as follows: GEO-MED CABG PACK PGYBK A & B, REF 89-5985.07, STERILE EO Use:
DeRoyal recalls custom sterile surgical packs with Terumo Over Pressure Safety Valve due to reported 'No Flow' issues. Affected packs have specific lot numbers and labels.
DeRoyalJan 22, 2018 - Lower riskMedical device
Valeris Medical, LLC recalls Apollo XT Suture Anchor, 5.5 x 15 Product Usage: Apollo XT Suture Anchors are intended for: Shoulder - Rotator Cuff
Valeris Medical recalls Apollo XT Suture Anchors (model XT-5515, lots 2358/2362/2363) due to incorrect material label. This could lead to improper use in shoulder, knee, and other repairs.
Valeris MedicalJan 22, 2018 - Lower riskMedical device
Aesculap Implant Systems LLC recalls DS Titanium Ligation Clip, used in laparoscopic surgery
Aesculap recalls DS Titanium Ligation Clips used in laparoscopic surgery for living donor kidney transplants. The clips were not approved for this use per 2017 publication.
AesculapJan 22, 2018 - Lower riskDrug
Astellas Pharma US Inc recalls Mycamine (micafungin) for Injection 100 mg/vial Single-Dose Vial Rx only Marketed by: Astellas Pharma US, Inc.
Astellas recalls Mycamine (micafungin) injection vials due to labeling error on declared strength. Affected vials have specific NDC and expiration dates. No action needed for safety, but verify your product.
AstellasJan 22, 2018 - Lower riskDrug
AbbVie Inc. recalls Ultane (sevoflurane), 250 mL, Inhalation Anesthetic, Rx only, Manufactured by: AbbVie Inc., North Chicago, IL 60064,
AbbVie recalls Ultane (sevoflurane) inhalation anesthetics due to potential container leaks from cap liner holes. This is a prescription-only product with specific lot numbers.
AbbVieJan 22, 2018 - Use cautionDrug
Ascent Pharmaceuticals, Inc. recalls Oxycodone Hydrochloride Tablets, USP 15 mg, 100 count bottles, Rx only, Manufactured for Camber Pharmaceuticals, Inc.,
Camber Pharmaceuticals recalls 45,875 bottles of 15mg Oxycodone tablets because the label is missing the required CII controlled substance symbol.
Camber PharmaceuticalsJan 22, 2018 - Lower riskFood
Mountain Rose Inc recalls Prickly Ash Bark Powder Herbal Supplement, packaged in food grade stand up plastic pouches or plastic bags depending on
Mountain Rose Inc recalls Prickly Ash Bark Powder herbal supplements due to potential Salmonella contamination. Consumers should check product labels for lot #23574-P and take appropriate action.
Mountain RoseJan 22, 2018 - Lower riskFood
Sun Noodle New Jersey, LLC recalls Sun Noodle brand Tonkotsu Ramen, Packaged in plastic clear clamshell, Banded with Tonkotsu label, distinguishable with
Sun Noodle recalls Tonkotsu Ramen due to incorrect flavor packet containing sardines instead of labeled tonkotsu. Check packaging for yellow band and UPC 085315400035.
Sun NoodleJan 22, 2018 - Lower riskFood
Divine Living recalls Divine Living Silver with harmonically structured frequencies A Wellness Solution 8 oz Ingredients: Structured Water,
Divine Living recalls 8oz Silver Wellness Solution products for containing unverified health claims. The Ohio Department of Agriculture notified the firm of dietary and health claims violations.
Divine LivingJan 22, 2018 - Lower riskMedical device
SIE AG, Surgical Instrument Engineering recalls The FEMTO LDV(TM)Z8 Femtosecond Surgical Laser The FEMTO LDV(TM)Z8 Femtosecond Surgical Laser is an ophthalmic surgical
SIE AG recalls FEMTO LDV Z8 Femtosecond Surgical Lasers after customer complaints of cataract procedure complications. The recall addresses usability and performance improvements for safer ophthalmic surgery.
SIE AGJan 21, 2018 - Use cautionMedical device
Hologic, Inc recalls Hologic Panther(R) Fusion(TM), Catalog number ASY-09600 Product Usage: The Panther instrument is a fully automated
Hologic recalls Panther Fusion devices with serial numbers 2090002307-2492 due to risk of glass panel falling and hitting operators during use.
HologicJan 20, 2018 - Stop using nowFood
ABH Nature's Products, Inc. recalls Arthri-D 120ct
ABH Nature's Products recalls Arthri-D 120ct due to potential Salmonella contamination. Check your lot number and distribution area for details.
ABH Nature's ProductsJan 20, 2018 - Use cautionVehicle
NEWMAR DUTCH STAR (2018) recall — Exterior Lighting
Newmar recalls 2017-2018 Dutch Star motorhomes because low beam headlights may not illuminate when high beams are on, reducing visibility.
NewmarJan 19, 2018 - Use cautionVehicle
KZRV DURANGO GOLD (2018) recall — Structure
KZRV is recalling 2017-2018 Durango Gold trailers with rear sofas that may block exit window visibility or access during emergencies. Owners should contact KZRV for a free back replacement.
KZRVJan 19, 2018 - Lower riskMedical device
Terumo Cardiovascular Systems Corporation recalls Flowmeter Module (accessory to Terumo Advanced Perfusion System 1). Provides the interface between the flow sensor and
Terumo recalls Flowmeter Module (accessory for Advanced Perfusion System 1) due to inaccurate flow readings that may not be easily detected during setup or use. Affected units have specific serial numbers.
TerumoJan 19, 2018 - Lower riskMedical device
Beckman Coulter Inc. recalls AutoMate 1200 Catalog Number ODL25120; AutoMate 1250 Catalog Number ODL25125; AutoMate 2500 Catalog Number ODL25250;
Beckman Coulter recalls AutoMate 1200, 1250, 2500, and 2550 lab systems with 2015 belts that may fail, causing cross-contamination. Affected units have specific serial numbers and catalog numbers.
Beckman CoulterJan 19, 2018 - Stop using nowMedical device
Mako Surgical Corporation recalls Restoris MCK Onlay Insert Extractor.
Mako Surgical recalls Restoris MCK Onlay Insert Extractor with possible hinge pin disassociation. Affected items include specific lot numbers from 2019-2023. Stop using immediately if you own this surgical device.
Mako SurgicalJan 19, 2018 - Lower riskMedical device
Implant Direct Sybron Manufacturing, LLC recalls SwishPlus Implant Intended for use in support for fixed bridgework.
Implant Direct recalls SwishPlus Implant for potential incorrect packaging that could lead to misuse in dental bridgework. Affected units include specific part numbers and lots.
Implant DirectJan 19, 2018 - Lower riskMedical device
Allison Medical, Inc. recalls InControl Insulin Syringes, Short Needle, 29 Gauge, 1CC
Allison Medical recalls InControl Insulin Syringes labeled as 'Short Needle' due to incorrect labeling. This may cause confusion about needle length for safe insulin administration.
Allison MedicalJan 19, 2018 - UnratedDrug
AMERICAN HEALTH PACKAGING recalls Aripiprazole Tablets, USP, 10 mg, 100 Tablets (10 x 10) unit dose blisters [NDC60687-179-11; UPC (01) 003 60687 179 11
American Health Packaging recalls 10 mg Aripiprazole tablets due to CGMP deviations affecting quality. No remedy specified in official notice.
American Health PackagingJan 19, 2018
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