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
34,893 found- Lower riskMedical device
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail, 125 DEG 11MM X 180MM
Zimmer Biomet recalls Affixus Hip Fracture Nails with potential assembly issues that could prevent proper function during hip fracture repair.
Zimmer BiometAug 7, 2017 - UnratedDrug
International Laboratories, Inc. recalls Pravastatin Sodium Tablets, USP, 40 mg, 30-count bottle, Rx only, Packaged for: International Laboratories, LLC. St.
International Laboratories recalls Pravast: 40mg tablets labeled as Pravastatin but contain Bupropion hydrochloride. This mix-up poses a risk of incorrect medication use. Consumers should check product labels and contact the company for details.
International LaboratoriesAug 7, 2017 - Lower riskFood
Taylor Farms Retail, Inc. recalls Taylor Farms Creamy Homestyle Coleslaw Kit, dressing included. Green Cabbage, Carrots, Red Cabbage and Creamy coleslaw
Taylor Farms recalls coleslaw kits with organic dressing containing egg and milk, not listed on labels. Consumers should check lot codes and contact for details.
Taylor FarmsAug 7, 2017 - Use cautionFood
Mary's Gone Crackers, Inc. recalls Mary's Gone Crackers Original Crackers: Organic, Gluten Free, Non-GMO, Vegan. 6.5 oz. (184 g) box; Ingredients: Whole
Mary's Gone Crackers recalls organic, gluten-free crackers due to plastic pieces found inside packages. Consumers should check UPC codes and contact the company for details.
Mary's Gone CrackersAug 7, 2017 - UnratedFood
Michele's Granola LLC recalls Michele s Toasted Muesli, 16 oz bags, 12 units per case
Michele's Granola LLC recalls 16oz Toasted Muesli bags from 2017 due to potential Listeria monocytogenes contamination. Consumers should avoid use until further notice.
Michele's GranolaAug 7, 2017 - Lower riskFood
Schnucks Markets Corporate Office recalls German chocolate cakes labeled as Schnucks Bakery Deluxe Petite Cake Chocolate Iced Yellow, Net Wt. 1 lb 1 oz (482 g),
Schnucks recalls German chocolate cakes labeled as 'Chocolate Iced Yellow' that contain pecans not listed on the label. Consumers should check product details for the specific recall.
SchnucksAug 7, 2017 - Stop using nowFood
Carla's Pasta, Inc. recalls CARLA'S PASTA, INC. BASIL PESTO SAUCE: BULK, Mfd. Date 06/20/17, KEEP FROZEN NET WT. 13.40 LBS (6.08 kg) 00021605014209
Carla's Pasta Inc. recalls basil pesto sauce produced June 20, 2017, due to potential Listeria monocytogenes contamination. Consumers should check product details and follow official recall instructions.
Carla's PastaAug 7, 2017 - Lower riskFood
Fresh Tex Produce, LLC recalls Valery Brand Maradol Papayas sold fresh in 35 pound boxes. Labeled grown and packed by Carica de Campeche
Fresh Tex Produce recalls Valery Brand Maradol papayas from July 10-13, 2017, due to Salmonella linked to a Mexican grower. Discard or avoid these papayas to prevent foodborne illness.
Valery BrandAug 7, 2017 - Stop using nowConsumer product
Firewood Recalls Vaporizers Due to Fire Hazard (Recall Alert)
Firewood is recalling all 4-inch vaporizers due to fire risk from electrical shorts. Consumers must stop using and contact Firewood for free repairs.
FirewoodAug 7, 2017 - Lower riskMeat & poultry
Hahn Brothers, Inc. Recalls Ready-To-Eat Ham Products Due To Misbranding and Undeclared Allergens
Hahn Brothers Inc. recalls 115,773 pounds of ready-to-eat ham products from Dec. 2015 to July 2017 due to malted barley, a known allergen, not being declared on labels.
Hahn BrothersAug 5, 2017 - Use cautionVehicle
FOREST RIVER XLR TOYHAULER (2017) recall — Tires
Forest River recalls 2017 XLR ToyHauler trailers with incorrect tire pressure placard (50psi vs 80psi) that could cause tire failure and crashes. Owners must get corrected placard installed free by dealers.
Forest RiverAug 5, 2017 - Lower riskMedical device
Encore Medical, Lp recalls MODIFIED/SPECIAL INSTRUMENT, TURON GLENOID REAMER, REAM AND RUN, Catalog Numbers: REF S-200956 - 5mm PIN, SIZE 46 REF
Encore Medical recalls specific Turon Glenoid Reamer models with incorrect spherical radius cutting surface that may cause improper bone cutting during surgery.
Encore MedicalAug 4, 2017 - Lower riskMedical device
Fujifilm Medical Systems U.S.A., Inc. recalls Fuji Computed Radiography Mammography Suite, FCRMS (for CR-IR363AWS) The Fuji Computed Radiography Mammography Suite
Fujifilm recalls mammography software that may assign duplicate image IDs, causing overwritten images in PACS systems. Affected units include specific software versions of the FCRMS system.
Fujifilm Medical SystemsAug 4, 2017 - Lower riskMedical device
Ultradent Products, Inc. recalls Ultradent Products, Inc. Paper Points, Size 50 PN #1559, 200 per container, sterile. Product Usage: The product is used
Ultradent recalls sterile Paper Points Size 50 (PN #1559) due to barcode label being placed under sterile barrier, risking contamination during dental procedures.
UltradentAug 4, 2017 - Use cautionMedical device
ZOLL Medical Corporation recalls OneStep CPR Complete, Adult Multi Function Electrodes, Part Numbers: 8900 0214 01 (case of 8 single electrodes, UDI:
ZOLL recalls adult CPR electrodes that may deliver pediatric energy levels with R Series defibrillators, causing potential harm. Affected units have a specific part number and lot number.
ZOLLAug 4, 2017 - Stop using nowDrug
Amgen, Inc. recalls Procrit Epoetin Alfa 40,000 units/mL single use vial For Intravenouse or Subcutaneous Use Only, Rx only, Manufactured
Amgen recalls Procrit Epoet: 40,000 units/mL vials with visible glass flakes that could cause injury during injection. Check NDC 59676-340-01, lots G290491A/B, expiring 06/18.
AmgenAug 4, 2017 - UnratedDrug
Pfizer Inc. recalls Quillivant XR methylphenidate HCl, for extended-release oral suspension, 750mg/150 mL total volume (When constituted
Pfizer recalls Quillivant XR methylphenidate HCl oral suspension due to failed dissolution specifications. This medication may not release properly when taken, potentially affecting effectiveness. Contact Pfizer for details.
PfizerAug 4, 2017 - Use cautionDrug
Degasa Sa De Cv recalls Povidone Iodine, USP Prep Solution, 10%, packaged in 1 gallon bottle, OTC, Manufactured for PSS World Medical, Inc.
Degasa recalls 1-gallon bottles of Povidone Iodine USP Prep Solution due to a labeling error where 7.5% product was labeled as 10%. Check your lot number.
DegasaAug 4, 2017 - Lower riskFood
EL Chilar Huff recalls El Chilar Whole Ginger, NET WT 1.25 Oz (35g)
El Chilar recalls 1.25 oz ginger with undeclared sulfites. Consumers should check lot number 918 (expiring 09/2018) for affected products.
El Chilar HuffAug 4, 2017 - Use cautionFood
Kilby Cream recalls Kilby Cream Ice Cream, Peach Size: 2.5 Gal
Kilby Cream recalls 2.5-gallon containers of Peach Ice Cream (Lot P1717) distributed in MD, PA, and DE due to improper temperature control during production.
Kilby CreamAug 4, 2017 - Use cautionVehicle
HYUNDAI SONATA HYBRID (2015) recall — Seat Belts
Hyundai recalls 2015 Sonata Hybrid vehicles with seat belt linkages that may detach during crashes, increasing injury risk. Owners must have seat belt connections inspected and repaired free by dealers starting April 7, 2017.
HyundaiAug 3, 2017 - Lower riskMedical device
Gyrus ACMI, Inc. recalls Gyrus ACMI Round Cutting Burrs - to be used with the Diego Elite system
Gyrus ACMI recalls round cutting burrs for Diego Elite systems made before August 2017 due to chattering when cutting bone. Affected units have specific catalog numbers and lots.
Gyrus ACMIAug 3, 2017 - Lower riskMedical device
Beckman Coulter Inc. recalls Power Processor 1K Stockyard. The Power Processor performs all pre-analytical sample tube preparation.
Beckman Coulter recalls Power Processor 1K Stockyard due to software issue that may cause sample tube retrieval during rack loading. Affected units have software version PLC V26R10.
Beckman Coul: 1K StockyardAug 3, 2017 - Lower riskMedical device
OrthoPediatrics Corp recalls Response 5.5/6.0 Spine System 7.0mm x 40mm Pedicle Screw Product Usage: Posterior non-cervical pedicle screw fixation
OrthoPediatrics recalls 7.0mm x 40mm pedicle screws for posterior non-cervical spine fixation due to color anodizing error with smaller screws. Affected units have model 00-1300-0: M82791-1 lot.
OrthoPediatricsAug 3, 2017 - Lower riskMedical device
Ivoclar Vivadent, Inc. recalls Heliomolar Refill 20x0.25g 110/A1, Product code 541501AN, Catalog number 541501
Ivoclar Vivadent recalls Heliomolar Refill 20x0.25g 110/A1 product due to overly sticky material causing handling issues during dental work. Affected units have specific batch numbers and expiration dates.
Ivoclar VivadentAug 3, 2017 - Lower riskDrug
Amneal Pharmaceuticals of New York, LLC recalls Lorazepam Oral Concentrate, USP, 2 mg/mL, 30 mL bottle, Rx only, Manufactured by: Amneal Pharmaceuticals Branchburg, NJ
Amneal Pharmaceuticals recalls Lorazepam Oral Concentrate 2 mg/mL 30mL bottles due to potential reversed dropper markings. This could lead to incorrect dosing. Check NDC codes and expiration dates for affected lots.
Amneal PharmaceuticalsAug 3, 2017 - Lower riskDrug
MEDLINE INDUSTRIES INC recalls Vitamin A&D Ointment (petroleum 93.5%), Skin Protectant, NET Wt. 0.18 OZ (5g), Manufactured for Medline Industries,
Medline recalls Vitamin A&D Ointment (petroleum 93.5%) due to labeling mixup where foil packets are incorrectly labeled as petroleum jelly. The boxes and outer case are correctly labeled as A&D ointment.
MedlineAug 3, 2017 - Lower riskDrug
KVK-Tech, Inc. recalls Phentermine HCL Capsules, USP 15 mg, packaged in a) 100-count bottles (NDC 10702-026-01), and b) 1000-count bottles
KVK Tech recalls 100-count and 1000-count 15mg Phentermine capsules due to impurities found in stability testing. These capsules may pose a risk of serious injury if taken.
KVK TechAug 3, 2017 - Lower riskFood
AGROSONS LLC recalls Papayas Maradol cavi, Grown and Packed by: CARICA DE CAMPECHE, DISTRIBUTED BY: AGROSONS LLC
Agrosons LLC recalls Papayas Maradol cavi due to potential Salmonella contamination. Consumers should avoid these products from lots 3044, 3045, and 3050.
AgrosonsAug 3, 2017 - Lower riskFood
Mary's Harvest Fresh Foods, Inc. recalls Kroger (QFC and Fred Meyer) brand, VEGETABLE MEDLEY KFK, Net wt. 10 oz, UPC 8 2676618505 4. Kroger Main & Vine brand,
Mary's Harvest Vegetable Medley KFK products recalled from Kroger stores due to potential E. coli O26 contamination. Consumers should avoid using these products.
Mary's HarvestAug 3, 2017
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