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Latest recalls
34,893 found- Stop using nowConsumer product
Fabri-Tech Recalls Infant Rompers Due to Choking Hazard; Sold Exclusively at Cracker Barrel Old Country Stores
Fabri-Tech recalls infant rompers with detachable shoulder buttons that pose a choking hazard. Return to Cracker Barrel stores for a full refund.
Fabri-TechAug 29, 2017 - Use cautionVehicle
HYUNDAI IONIQ ELECTRIC (2017) recall — Hybrid Propulsion System
Hyundai is recalling 2017 Ioniq Electric vehicles with a potential risk of crash if coolant contacts the EPCU. Owners will receive free repairs to fix the manufacturing defect.
HyundaiAug 28, 2017 - Use cautionVehicle
FORD F-350 SD (2017) recall — Seat Belts
Ford is recalling 2017 F-350 SD trucks with potentially inadequately attached left rear seat belt buckles. This could increase injury risk during crashes. Owners must have seat belt assemblies inspected and repaired by dealers.
FordAug 28, 2017 - Stop using nowVehicle
FORD EXPLORER (2017) recall — Wheels
Ford recalls certain wheel hub bearing assemblies for 2011-2017 Ford Explorer 4X2 vehicles due to a risk of the wheel separating.
FordAug 28, 2017 - Use cautionVehicle
FORD TAURUS (2017) recall — Steering
Ford is recalling 2017 Taurus vehicles with potentially detachable heat shields that could overheat steering gear, increasing crash risk. Owners must have heat shield fasteners inspected and replaced free by dealers.
FordAug 28, 2017 - Stop using nowVehicle
FORD MUSTANG (2017) recall — Air Bags
Ford is recalling 2017 Mustang vehicles with a potential air bag inflator rupture that could cause serious injury or death during a crash.
FordAug 28, 2017 - Use cautionVehicle
FORD FOCUS (2017) recall — Seat Belts
Ford is recalling 2017 Focus vehicles with potentially weak seat backs that could increase crash injury risk. Owners must have seat backs inspected and replaced free of charge by dealers.
FordAug 28, 2017 - Lower riskMedical device
St Jude Medical Inc. recalls Fortify VR - Model Numbers: CD1231-40 and CD1231-40Q; Fortify ST VR, Model Numbers: CD1241-40 and CD1241-40Q; Fortify
St Jude Medical is a leading manufacturer of medical devices, implants, and solutions for cardiac care, neurosurgery, and more. Explore their products and innovations.
St Jude MedicalAug 28, 2017 - Use cautionMedical device
Zimmer Biomet, Inc. recalls Persona Partial Knee System Product Usage: The Persona Partial Knee System instruments are used by a surgeon to
Zimmer Biomet recalls Persona Partial Knee System instruments due to potential fracture of the Impactor Pad during knee replacement surgery. Affected items have specific lot numbers and item numbers.
Zimmer BiometAug 28, 2017 - Lower riskMedical device
St Jude Medical Inc. recalls Assurity MRI Model Numbers: PM1272, PM2272 Implantation of a single-chamber pulse generator, dual-chamber pulse
St Jude Medical is a leading manufacturer of medical devices, including pacemakers, defibrillators, and other cardiac devices.
St Jude MedicalAug 28, 2017 - Lower riskDrug
Mckesson Packaging Services recalls Propafenone Hydrochloride tablets, 150 mg, packaged in 10 x 10 unit dose cards (100-count box), Rx only, Manufactured
Mckesson Packaging Services recalls 150mg Propafenone Hydrochloride tablets with moisture content out of specification. Rx-only medication may pose safety risks due to improper moisture levels.
Mckesson Packaging ServicesAug 28, 2017 - Lower riskFood
Tomanetti Food Products Inc recalls 12" homestyle pizza crusts packed 18 to a case (no consumer packaging) labeled as: Tomanetti Pizza Crusts with the
Tomanetti Food Products recalls 12" pizza crusts with small flexible plastic pieces. Consumers should check for the 18-12" Homestyle 9111 block code and keep frozen until contacted.
TomanettiAug 28, 2017 - Lower riskFood
Bateman Community Living recalls Breaded Fish with Vera Cruz Sauce; In 13.4 oz 3 compartment tray that has the fish, rice pilaf and green peas. Item
Bateman Community Living recalls 13.4oz breaded fish trays with missing allergen labels. The product may contain unlisted wheat and incorrect fish type. Consumers should check lot codes and contact for details.
Bateman Community LivingAug 28, 2017 - Lower riskFood
GONZALEZ WHOLESALE DISTRIBUTOR,L recalls Primera Negra, Artificial Vanilla Flavoring NET WT 4 OZ and 8 OZ
Gonzalez Wholesale recalls Primera Negra Artificial Vanilla Flavoring (4oz/8oz) due to coumarin content. Consumers should check lot numbers and contact for details.
Gonzalez WholesaleAug 28, 2017 - Use cautionMeat & poultry
Blossom Foods, LLC Recalls Frozen Meat Products Due to Misbranding and Undeclared Allergens
USDA recalls 15,092 pounds of frozen beef, chicken, and pork products due to soy and wheat allergens not declared on labels. Consumers urged to throw away or return recalled items.
Blossom FoodsAug 26, 2017 - Use cautionMeat & poultry
Ronald A. Chisholm, Ltd. Recalls Pork Belly Products Produced Without Benefit of Import Inspection
USDA FSIS recalls 12,169 pounds of skinless pork belly products from Canada that were not inspected at U.S. entry. Consumers urged not to consume; products should be thrown away or returned.
Ronald A. ChisholmAug 26, 2017 - Use cautionMeat & poultry
DiLuigi Foods Inc. Recalls Chicken Sausage Products Due to Misbranding and Undeclared Allergens
USDA recalls DiLuigi chicken breakfast sausage products from 2017 due to undeclared soy lecithin allergen. Consumers urged to stop using recalled items.
DiLuigi FoodsAug 25, 2017 - Use cautionVehicle
FOREST RIVER XLR (2018) recall — Equipment
Forest River is recalling 2018 XLR ToyHaulers with incorrect tire and rim placards that could lead to crashes if wrong tires are installed. Owners must get a corrected placard to comply with safety standards.
Forest RiverAug 25, 2017 - Lower riskMedical device
Keystone Dental Inc recalls Stage-1¿ RDS Indexed Abutment for RDS Stage-1¿ Single Stage Implants Keystone s implants are intended for use in
Keystone Dental recalls Stage-1 RDS Indexed Abutments with incorrect expiration date (2202-06 instead of 2:2022-06). Affected units may expire prematurely. Contact for replacement.
Keystone DentalAug 25, 2017 - Lower riskMedical device
Zimmer Biomet, Inc. recalls AGC 2000 LP Patella, labeled as AGC Porous Patellar SM, Model Number 150802. Product Usage: For use in Total Knee
Zimmer Biomet recalls AGC 2000 LP Patella implants (Model 150802) due to over-molding causing nonconforming outside diameter. This may affect surgical fit in total knee replacements.
Zimmer BiometAug 25, 2017 - Lower riskMedical device
Zimmer Biomet, Inc. recalls G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended for use in hip arthroplasty cases which involves the removal of
Zimmer Biomet recalls G7 Dual Mobility Liner 4:44MM F products due to potential size mismatch with E-42MM liners. This could affect hip replacement surgery outcomes. Learn if your product is affected and what to do.
Zimmer BiometAug 25, 2017 - Lower riskMedical device
Biomerieux Inc recalls VITEK(R) 2 GP, REF 21342, IVD, UDI 03573026131920, bioMerieux, Inc. VITEK(R) 2 is an automated system consisting of
BioMérieux recalls VITEK 2 GP ID system with specific lot numbers due to atypical negative reactions in Enterococcus casseliflavus QC testing, potentially causing false negative results.
BioMérieuxAug 25, 2017 - Use cautionVehicle
THOR MOTOR COACH FREEDOM ELITE (2018) recall — Equipment
Thor Motor Coach is recalling 2018 Freedom Elite RVs due to propane hose sagging that could cause leaks and fire. Owners must contact TMC for free repairs by October 13, 2017 deadline.
Thor Motor CoachAug 24, 2017 - Lower riskMedical device
Smiths Medical ASD Inc. recalls Graseby 3300 Pump and Graseby 3000 Series Pump Accessories Patient controlled syringe pump. Use for Infusion
Smiths Medical recalls Graseby 3300 Patient Controlled Syringe Pumps with mismatched lock and key. Affected models include 0128-0001 to 069850. Contact for remedy.
Smiths MedicalAug 24, 2017 - Lower riskMedical device
Beckman Coulter Inc. recalls Lyophilized Chemistry Calibrator Level 1 Product Usage: Beckman Coulter Chemistry Calibrators are intended for use when
Beckman Coulter recalls two specific lots of lyophilized chemistry calibrators (6101K51 and 6101K61) that must be used in exact pairs to avoid calibration errors. Using mismatched pairs may cause inaccurate test results.
Beckman CoulterAug 24, 2017 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls AArtis Q/ Q.Zen biplane Artis zee biplane Product Usage: Artis is a family of dedicated angiography systems developed
Siemens recalls Artis Q and Q.Zen biplane angiography systems due to potential ceiling mount screw quality issues that could affect safety standards.
SiemensAug 24, 2017 - Lower riskMedical device
Firefly Medical, Inc. recalls IVEA Product Part Number 16100 Model 500A
Firefly Medical recalls IVEA Model 500A (serial numbers listed) due to dowel pins that can rotate out of leg castings after repeated use, potentially causing instability.
Firefly MedicalAug 24, 2017 - Lower riskFood
Dedinas Franzak Enterprises dba Cheeze Kurls Inc.c. recalls Big Win Butter Popcorn, 5 oz., Butter Popcorn Artificially Flavored; Uncle Ray's 10 oz., Gourmet Select 12 oz., Gold
Cheeze Kurls recalls Big Win Butter Popcorn and Uncle Ray's popcorn products due to undeclared milk allergen. Consumers should check UPCs and stop using if they have these items.
Cheeze KurlsAug 24, 2017 - Lower riskFood
House of Spices India, Inc. recalls Laxmi Rusks, 10.58 OZ (300 gram) bags; UPC Code: 7 23246 26482 0
House of Spices India, Inc. recalls Laxmi Rusks bags due to potential undeclared soy content. Affected products include specific UPC codes and batch numbers. Consumers should check their purchases and contact the company for details.
House of SpicesAug 24, 2017 - Lower riskFood
Handsome Brook Farm, LLC recalls Handsome Brook Farm Soy-Free Organic Pasture-Raised Eggs, UPC 8-66332-00011-4. The product is packaged in a tan, paper
Handsome Brook Farm Soy-Free Organic Pasture-Raised Eggs with Julian Date Codes 201, 208, or 222 may have mold. Consumers should check carton labels and discard if mold is present.
Handsome Brook FarmAug 24, 2017
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