The Recall Desk

Archive

January 2017 recalls

913 recalls were announced in January 2017.

What the numbers show

Critical
104
Severe
443
High
205
Moderate
130
Low
31

Of the 913 recalls this month scored against our rubric, 11% are Critical, 49% are Severe.

Which agencies issued them

101–200 of 913

  • HighFDA (Devices)·Z-1046-2017·2017-01-25

    Merge Cardio software recalled for potential image loading errors

    Merge Healthcare is recalling Merge Cardio software versions 9.0 through 10.1.2 because a specific user action may cause images to be missing, potentially leading to incorrect diagnosis or treatment.

    Product
    Merge Cardio software. Product Usage: Merge Cardio is a system intended to be used to acquire, store, print, transfer, and archive clinical information including images, Hemodynamic studies and reports, measurements (via import from DICOM Structured Reporting, text files or
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1264-2017·2017-01-25

    Herr Foods Recalls Chipotle Potato Chips Due to Salmonella Risk

    Herr Foods is recalling 2.0 oz. Chipotle flavored Kettle Potato Chips because the seasoning contains a milk ingredient with a potential risk of Salmonella contamination.

    Product
    Dried Smoke Chipotle Flavored Kettle Cooked Potato Chips 2.0 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1034-2017·2017-01-25

    Ultradent NanoTips 30g Dental Tips Recalled for Loose Cannula

    Ultradent Products, Inc. is recalling NanoTips 30g dental tips because the stainless steel cannula may detach from the base, posing a risk during intra-oral procedures.

    Product
    NanoTips 30g 20pk, 100pk PN 1240, 1426 Description: NanoTips are injection molded royal blue tips that contain stainless steel 30-gauge cannula to aid in the delivery of chemicals. The NanoTip base is made from a polypropylene copolymer. The stainless steel cannula is made from
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1295-2017·2017-01-25

    High Liner Breaded Shrimp Recalled for Undeclared Milk and Eggs

    High Liner Foods is recalling breaded shrimp containing undeclared milk and eggs. The product was distributed in seven states.

    Product
    FPI Breaded Round Shrimp Tail-On 1001990, 12-8 oz. cartons per master case, Master case 6 lbs. (2.72 kg)
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-1259-2017·2017-01-25

    NY Rye Deli Loaf Recalled for Undeclared Soy Allergen

    Great Northern Bakehouse is recalling NY Rye Deli Loaves because they contain undeclared soy lecithin from a pan spray.

    Product
    NY Rye Deli Loaf, each loaf has a net wt. 32 oz.. No UPC as this is for food service only.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1253-2017·2017-01-25

    Birdman Bread Recalled for Undeclared Soy Allergen in Montana

    Great Northern Bakehouse is recalling Birdman Bread sold in Montana because it contains undeclared soy lecithin from a pan spray.

    Product
    Birdman Bread, each loaf has net wt. 24 oz and 32 oz.. The UPC code ia 6 36428 10200 4.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1286-2017·2017-01-25

    Bakers of Paris Croissants Recalled for Undeclared Egg Allergen

    Bakers of Paris is recalling assorted croissants sold in Northern California because the packaging fails to declare egg, a major allergen, in the ingredients list.

    Product
    Assorted Croissant:: sold in 4 pack clamshell package. Ingredients: Plain Croissant: ( dough [enriched unbleached flour (wheat flour, malted barley flour, niacin, iron, thiamin, mononitrate, riboflavin, folic acid) water, butter, sugar, milk, yeast, salt, ascorbic acid, enzymes}
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1272-2017·2017-01-25

    Hungry Heart Chocolate Chip Sea Salt Cookies Recalled for Undeclared Allergens

    Hungry Heart Bakery is recalling Chocolate Chip Sea Salt Cookies due to undeclared wheat and soy. The product was distributed in Oregon.

    Product
    Chocolate Chip Sea Salt Cookies, Hungry Heart brand. Product is packaged in a clear cello bags, heat sealed. 1 unit per bag. Net wt. 2.75 oz. (78g).
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1038-2017·2017-01-25

    Endologix AFX Endovascular AAA System Instructions for Use Update

    Endologix updated the Instructions for Use for the AFX Endovascular AAA System to address endoleak Type IIIB.

    Product
    AFX Endovascular AAA System, Endoleak Type IIIB; The AFX Endovascular AAA System is intended for endovascular treatment of patients with abdominal aortic or aortoiliac aneurysms (AAA).
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0433-2017·2017-01-25

    Novum Pharma Recalls Subpotent Novacort Gel Sample Packets

    Novum Pharma is recalling Novacort Gel sample packets because the pramoxine hydrochloride content was found to be out of specification.

    Product
    Novacort Gel Sample Packets (2% hydrocortisone acetate, 1% pramoxine HCl), 10-count Carton of 1.0 g sample packets), NDC 69646-704-38 (10 ct. Carton of 1gm samples) / NDC 69646-704-01 (Individual 1gm Samples within Carton), Rx Only, Novum Pharma LLC, Chicago, IL 60654
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1032-2017·2017-01-25

    Exactech Recalls Alteon Neck Preserving Stems Due to Incorrect GTIN Labels

    Exactech is recalling 98 Alteon Neck Preserving Stems because they were labeled with incorrect Global Trade Item Numbers (GTINs) that identify them as different devices.

    Product
    Alteon Neck Preserving Stem, Standard Offset, Plasma Coated, Size 6
    Category
    Medical Device
    Distribution
    13 states
  • ModerateFDA (Drugs)·D-0435-2017·2017-01-25

    Sandoz Recalls Subpotent Donepezil Hydrochloride Tablets

    Sandoz Inc. is recalling specific lots of Donepezil Hydrochloride 10 mg tablets because they failed potency tests. The medication may not contain the full prescribed dose.

    Product
    Donepezil Hydrochloride Tablets, 10 mg, packaged in a) 30-count bottles (NDC 0781-5275-31) and b) 1000-count bottles (NDC 0781-5275-10), Rx only, Manufactured in India by Sandoz Private Ltd for Sandoz Inc., Princeton, NJ 08540.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1042-2017·2017-01-25

    Smith & Nephew RENASYS GO Power Supply Recalled for Regulatory Clearance

    Smith & Nephew is recalling RENASYS GO Negative Pressure Wound Therapy External Power Supply Units because they lack 510(k) clearance for a design modification.

    Product
    Smith & Nephew, RENASYS GO Negative Pressure Wound Therapy External Power Supply Unit, Rx only. Intended for patients who would benefit from a suction device to help promote wound healing by removing fluids, including irrigation and body fluids, wound exudates and infectious
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1031-2017·2017-01-25

    Exactech Recalls Polyethylene Acetabular Liners Due to Incorrect GTIN Labels

    Exactech, Inc. is recalling 12 polyethylene acetabular liners because they were labeled with incorrect Global Trade Item Numbers (GTINs).

    Product
    AcuMatch A-Series Connexion GXL Enhanced Polyethylene Acetabular Liner, 15, +5 mm Lateralized, 36 mm I.D., Size J.
    Category
    Medical Device
    Distribution
    13 states
  • ModerateFDA (Drugs)·D-0434-2017·2017-01-25

    Perrigo Recalls Clindamycin and Benzoyl Peroxide Gel Due to Mold

    L. Perrigo Company is recalling 162,534 tubes of Clindamycin Phosphate and Benzoyl Peroxide Gel because a small number of tubes may contain mold on the cap.

    Product
    CLINDAMYCIN PHOSPHATE AND BENZOYL PEROXIDE — CLINDAMYCIN PHOSPHATE AND BENZOYL PEROXIDE (CLINDAMYCIN, BENZOYL PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1030-2017·2017-01-25

    Exactech Recalls Novation Cemented Plus Femoral Stems Due to Labeling Error

    Exactech is recalling 79 Novation Cemented Plus Femoral Stems because they were labeled with incorrect Global Trade Item Numbers (GTINs).

    Product
    Novation Cemented Plus Femoral Stem, 12/14, Collared, Standard Offset, Matte, Cemented, Size 15.
    Category
    Medical Device
    Distribution
    13 states
  • ModerateFDA (Devices)·Z-1024-2017·2017-01-25

    Zimmer Biomet Recalls ArComXL Polyethylene Liners Due to Labeling Mismatch

    Zimmer Biomet is recalling 36 units of ArComXL polyethylene liners because packaging labels did not match the physical product, posing a risk of surgical delay.

    Product
    RingLoc ArComXL Highly Crosslinked Polyethylene Liners ArComXL High Wall +3mm Liners Size 23 item XL-108323 ArComXL MaxRom +3mm Liners Size 23 item XL-108223
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1052-2017·2017-01-25

    Carestream Ultrasound Systems Recalled for Software Measurement Unit Error

    Carestream Health Inc. is recalling Touch Prime and Touch Prime XE ultrasound systems due to a software error that may display incorrect measurement units.

    Product
    Carestream Touch Prime, Catalog # 1738830, and Touch Prime XE, Catalog # 1738822, Ultrasound System Diagnostic ultrasound imaging or fluid flow analysis of the human body
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-1025-2017·2017-01-25

    Zimmer Biomet Recalls ArComXL Polyethylene Bearings Due to Labeling Mismatch

    Zimmer Biomet is recalling 19 ArComXL Polyethylene Bearings because packaging labels did not match the physical product inside, posing a risk of surgical delay.

    Product
    Active Articulation ArComXL Polyethylene Bearings Active Articulation ArComXL Bearings item XL-200152
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1035-2017·2017-01-25

    Endologix AFX Endovascular AAA System Clinical Data Correction

    Endologix is correcting cumulative clinical data reports for the AFX Endovascular AAA System and Powerlink System. This action applies to procedures conducted after June 2013.

    Product
    AFX Endovascular AAA System, Endoleak Type IIIA
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1037-2017·2017-01-25

    Endologix AFX Endovascular AAA System Instructions for Use Updated

    Endologix updated the Instructions for Use and modified the AFX Endovascular AAA System. The correction applies to procedures conducted after July 2015.

    Product
    AFX Endovascular AAA System, Endoleak Type IIIA Common Name: AFX Bifurcated and Accessory Stent Grafts Classification Name: System, Endovascular Graft, Aortic Aneurysm Treatment The AFX Endovascular AAA System is intended for endovascular treatment of patients with abdomin
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1039-2017·2017-01-25

    Endologix AFX Endovascular AAA System Instructions for Use Update

    Endologix is updating the Instructions for Use and implementing modifications to the AFX Endovascular AAA System.

    Product
    AFX Endovascular AAA System, Endoleak Type: IIIB Common Name: AFX Bifurcated and Accessory Stent Grafts Classification Name: System, Endovascular Graft, Aortic Aneurysm Treatment The AFX Endovascular AAA System is intended for endovascular treatment of patients with abdomi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1040-2017·2017-01-25

    Beckman Coulter AutoMate 2500 Family Recalled for Operating System Update

    Beckman Coulter is recalling four AutoMate 2500 Family units in Maryland to update the PC image for Windows 10 compatibility.

    Product
    AutoMate 2500 Family Catalog No. ODL25120 AutoMate 1200, ODL25125, AutoMate 1250, ODL25250 AutoMate 2500, ODL25255 Automate 2550. AutoMate 1200/1250/2500/2550 System Series is a semi-open, pre- and post-analytical sample processing and sorting system. The base system automates
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1023-2017·2017-01-25

    Medacta M.U.S.T. Rods Recalled for Damaged Packaging and Sterility Issues

    Medacta USA Inc. is recalling 82 M.U.S.T. Rods due to damaged packaging and lack of sterility assurance. The recall covers units distributed in the US and several international countries.

    Product
    Medacta International SA, M.U.S.T. Rod, REF 03.50.433, Size 5.5mm, Length 480mm, Type Straight, Mat Co-Cr-Mo The rods act as a connector between the different pedicle screws to create a stable construct for the stabilization and fusion of the lumbar and thoracic spine. Indic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1045-2017·2017-01-25

    DICOM GRID Recalls Ambra PACS Software Due to Image Display Error

    DICOM GRID Inc. is recalling Ambra PACS software version V3.16.13.0 because a defect causes diagnostic images to appear washed out, potentially affecting image analysis.

    Product
    Ambra PACS UDI: +AMBRHEALTHSOLUTIONS0/$$+7_V3.16.13.0R Software Version Number: V3.16.13.0 Intended for use as a primary diagnostic and analysis tool for diagnostic images.
    Category
    Medical Device
    Distribution
    27 states
  • ModerateFDA (Drugs)·D-0436-2017·2017-01-25

    Town and Country Recalls Subpotent HCG Vials Due to Failed Potency

    Town and Country Compounding is recalling 101 vials of HCG because potency testing showed 74%, below the required 80-125% range.

    Product
    HCG (Chorionic Gonadotropin Lyopholized) II, 1000 unit vial, Rx only, Prepared by Town & Country, Compounding & Consultation Services, 106 Prospect St - 1st FL, Ridgewood, NJ 07459
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0977-2017·2017-01-25

    BioMerieux NucliSENS magnetic extraction reagents recalled for performance drift

    BioMerieux SA is recalling NucliSENS magnetic extraction reagents because a performance drift was observed in BK virus testing for certain silica batches.

    Product
    NucliSENS magnetic extraction reagents, For in vitro diagnostic use, Product Usage: NucliSENS miniMAG¿ is intended to be used for the extraction of total nucleic acids from biological specimens.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1261-2017·2017-01-25

    Safeway Signature Kitchens Tuna Chunk Light Recalled for Decomposition

    Safeway is recalling Signature Kitchens Tuna Chunk Light in 20 oz, 12 oz, and 5 oz sizes due to failed sensory analysis and decomposition.

    Product
    Signature Kitchens Tuna Chunk Light 20 oz. (4 pack), 12 oz., 5 oz. UPC Codes: 2113033549, 2113035609, 2113035612
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1049-2017·2017-01-25

    Endologix AFX2 Endovascular AAA System Recall for Updated Endoleak Information

    Endologix is recalling the AFX2 Endovascular AAA System to provide updated information regarding Type III endoleak rates and patient surveillance.

    Product
    AFX2 Endovascular AAA System Item No. Item Description F00820-01 BEA28-120/I20-40 F00820-02 BEA28-100/I20-40 F00820-03 BEA28-80/I20-40 F00820-06 BEA28-120/I16-40 F00820-07 BEA28-100/I16-40 F00820-08 BEA28-80/I16-40 F00820-09 BEA28-60/I16-40 F00820-16 BEA28-110/I20
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1262-2017·2017-01-25

    Safeway Recalls Signature Kitchens Tuna Due to Decomposition

    Safeway is recalling 177 cases of Signature Kitchens Tuna Solid White 12 oz. cans because they failed sensory analysis and showed signs of decomposition.

    Product
    Signature Kitchens Tuna Solid White 12 oz. UPC Codes: 2113035611
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1050-2017·2017-01-25

    Binding Site Freelite Human Lambda Free SPAPlus Kit Recalled for Calibration Drift

    The Binding Site Group is recalling 1,002 units of the Freelite Human Lambda Free SPAPlus Kit because calibration curve activity increased over time.

    Product
    Human Lambda Free SPAPlus Kit Product Code: LK018.S Freelite aids in the detection and monitoring of Multiple Myeloma and related diseases.
    Category
    Medical Device
    Distribution
    11 states
  • ModerateFDA (Food)·F-1331-2017·2017-01-25

    O'Pelle Bakery Egg Bagels Recalled for Missing Yellow 5 Labeling

    O'Pelle Enterprises is recalling frozen raw Egg Bagels because the label fails to declare Yellow 5. The product was distributed only within Florida.

    Product
    Opelle Bakery Egg Bagel (B-105), case of 96 (4 oz.), Frozen Raw.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1041-2017·2017-01-25

    Smith & Nephew RENASYS GO Wound Therapy Recall for Clearance Issue

    Smith & Nephew is recalling RENASYS GO Negative Pressure Wound Therapy devices because they lack 510(k) clearance for a design modification.

    Product
    Smith & Nephew, RENASYS GO Negative Pressure Wound Therapy, Rx only. Intended for patients who would benefit from a suction device to help promote wound healing by removing fluids, including irrigation and body fluids, wound exudates and infectious materials. Used for chronic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1043-2017·2017-01-25

    Optilite Freelite Lambda Free Kit Recalled for Inaccurate Test Results

    The Binding Site Group is recalling 809 Optilite Freelite Lambda Free Kits because specific lots produce test results that are approximately 33% lower than expected.

    Product
    Optilite Freelite Lambda Free Kit Product Code: LK018.OPT, LK018.OPT.A Protein testing kit.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Food)·F-1330-2017·2017-01-25

    O'Pelle Bakery Egg Bagels Recalled for Missing Yellow 5 Labeling

    O'Pelle Enterprises is recalling frozen raw Egg Bagels because the label fails to declare Yellow 5, a common food dye.

    Product
    Opelle Bakery Egg Bagel (C-105), case of 60 (3.5 oz.), Frozen Raw.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1055-2017·2017-01-25

    Binding Site Digital RID Plate Reader Recalled for Software Defect

    The Binding Site Group is recalling Digital RID Plate Readers and software because a defect may prevent the system from flagging out-of-range quality control results.

    Product
    Digital RID Plate Reader and Software Product Code: AD400
    Category
    Medical Device
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-1048-2017·2017-01-25

    Endologix AFX Endovascular AAA System Recall for Updated Endoleak Information

    Endologix is recalling 34 units of the AFX Endovascular AAA System to provide updated information regarding Type III endoleak rates and patient surveillance.

    Product
    AFX Endovascular AAA System Item Number Item Description F0070305 A2525/C75 V F0070308 A2828/C75 V F0070312 A3434/C80 V f00553 I1616/C55F SA F00556 I2013/C70F SA F00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1333-2017·2017-01-25

    Starkey Spring Water Recalled for Arsenic Detection in Sample

    Starkey Water is recalling 300 cases of 16.9 oz glass bottles of Starkey Spring Water because 12 ppb of arsenic was detected in a water sample.

    Product
    Starkey Spring Water, 16.9 FL oz. (500 mL) glass bottle. packed 15 bottles in cardboard box. Product UPC 8 11904 02000 7. Case UPC 8 11904 02002 1.
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-1047-2017·2017-01-25

    Endologix Updates Instructions for Use for AFX Endovascular AAA System

    Endologix is updating the Instructions for Use and making modifications to the AFX Endovascular AAA System. This applies to procedures conducted after October 2015.

    Product
    AFX Endovascular AAA System, Endoleak Type IIIA Product Usage: The AFX Endovascular AAA System is intended for endovascular treatment of patients with abdominal aortic or aortoiliac aneurysms (AAA).
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1054-2017·2017-01-25

    Endologix Updates Instructions for Use for AFX Endovascular AAA System

    Endologix is recalling 17,139 units of the AFX Endovascular AAA System to update the Instructions for Use and implement device modifications.

    Product
    AFX Endovascular AAA System, Endoleak Type IIIB Common Name: AFX Bifurcated and Accessory Stent Grafts Classification Name: System, Endovascular Graft, Aortic Aneurysm Treatment
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Drugs)·D-0431-2017·2017-01-25

    Teva Recalls Risedronate Sodium Tablets for Failed Dissolution Specifications

    Teva Pharmaceuticals is recalling 6,800 cartons of Risedronate Sodium Delayed-release Tablets, 35 mg, because they failed dissolution specifications.

    Product
    Risedronate Sodium Delayed-release Tablets, 35 mg, Once-a-Week, 1 tablet per blister (NDC 0093-5509-19), packaged in 4 blisters per carton (NDC 0093-5509-44), Rx only, TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·010-2017·2017-01-25

    Atlas Meat Company Recalls Pork Sausage Due To Undeclared MSG

    Atlas Meat Company is recalling pork sausage products because they may contain monosodium glutamate (MSG), which is not declared on the label.

    Product
    Atlas Meat Company — Atlas Meat Company Recalls Pork Products Due To Misbranding
    Category
    Food
    Distribution
    2 states
  • LowFDA (Devices)·Z-0976-2017·2017-01-25

    BioMerieux Recalls MagSIL Magnetic Silica Reagents Due to Performance Drift

    BioMerieux SA is recalling 3,723 units of MagSIL (NucliSENS easyMAG Magnetic Silica) worldwide due to observed performance drift in BK virus testing.

    Product
    MagSIL (NucliSENS easyMAG Magnetic Silica), Product Usage: The NucliSENS¿ easyMAG¿ system is an in vitro diagnostic medical device and is intended for the automated isolation (purification and concentration) of total nucleic acids (RNA/DNA) from biological specimens.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V052000·2017-01-24

    Ford Recalls 2016 Focus and C-Max for Floor Pan Welding Defect

    Ford is recalling 2016 Focus and C-Max vehicles because improperly welded floor pan joints may reduce structural integrity, increasing injury risk in a crash.

    Product
    FORD — FORD C-MAX, FOCUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17071·2017-01-24

    HP Recalls Lithium-Ion Notebook Batteries Due to Fire and Burn Hazards

    HP is expanding a recall of about 101,000 lithium-ion batteries for HP and Compaq notebook computers because they can overheat, posing fire and burn risks.

    Product
    Lithium-ion batteries used in HP notebook computers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V051000·2017-01-24

    Toyota Recalls 2016-2017 Tundra Trucks for Rear Bumper Defect

    Toyota is recalling 2016-2017 Tundra trucks with resin rear bumpers because the brackets may break if stepped on, posing an injury risk.

    Product
    TOYOTA — TOYOTA TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V053000·2017-01-24

    Ford Recalls 2017 F-150 Trucks Due to Instrument Cluster Power Loss

    Ford is recalling 2017 F-150 trucks because the instrument cluster may lose power in cold weather, potentially hiding the transmission gear position and increasing crash risk.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V050000·2017-01-23

    Autocar Recalls 2013-2016 Xpeditor Trucks Due to Brake Defect

    Autocar is recalling 38 Xpeditor trucks from 2013-2016 because over-braking can cause S-cam tube bolts to loosen, leading to unexpected brake engagement and increased crash risk.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E005000·2017-01-23

    IH Parts Recalls Steering Tie Rod Adjusters for Fracture Risk

    IH Parts America Inc. is recalling specific steering tie rod adjusters for International Scout vehicles because they may fracture, affecting steering capability and increasing crash risk.

    Product
    STEERING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·17V047000·2017-01-20

    BMW Recalls 2000-2003 Models for Driver Air Bag Inflator Rupture Risk

    BMW is recalling specific 2000-2003 3, 5, and X5 series vehicles because replacement driver-side air bag inflators may rupture during deployment, posing a risk of serious injury or death.

    Product
    BMW — BMW 323, 320, 325, 330
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·009-2017·2017-01-20

    Hans Kissle Recalls Ready-To-Eat Chicken Bowls Due to Processing Defect

    Hans Kissle Company is recalling approximately 6,348 pounds of ready-to-eat chicken bowls due to a potential process defect that could allow bacterial pathogens to survive.

    Product
    Hans Kissle Company, LLC — Hans Kissle Company, LLC. Recalls Ready-To-Eat Chicken Products Due To Potential Processing Deviation
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V046000·2017-01-20

    Maserati Recalls 2014-2017 Models for Seat Wiring Fire Risk

    Maserati is recalling 39,381 vehicles due to a front seat wiring harness defect that may cause an electrical short and increase the risk of a fire.

    Product
    MASERATI — MASERATI QUATTROPORTE, GHIBLI, LEVANTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V048000·2017-01-20

    Walker Recalls 2014-2017 Food Grade Tank Trailers for Underride Guard Defect

    Walker is recalling 2014-2017 Food Grade Tank Trailers because weld joints on the underride guard may crack, potentially causing the guard to detach and become a road hazard.

    Product
    WALKER — WALKER FOOD GRADE TANK TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17E004000·2017-01-20

    New Haven Recalls Wheelchair Securement Tiedowns Due to Crash Risk

    The New Haven Companies is recalling Safe Haven Wheelchair Securement Tiedowns because they may not adequately secure a wheelchair in a crash, increasing injury risk.

    Product
    EQUIPMENT ADAPTIVE/MOBILITY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V044000·2017-01-20

    Airstream Recalls 2017 Trailers Due to Incorrect Tire Certification Labels

    Airstream is recalling 2017 Sport, International, and Flying Cloud trailers because incorrect tire labels could lead to overinflation and tire blowouts.

    Product
    AIRSTREAM — AIRSTREAM SPORT, INTERNATIONAL, FLYING CLOUD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17070·2017-01-19

    Trek Recalls 720 Disc Bicycles Due to Wheel Spoke Fall Hazard

    Trek is recalling 720 Disc bicycles and wheel sets because broken spokes can contact the brake caliper, posing a fall hazard to riders.

    Product
    Trek 720 Disc bicycles and wheel sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V041000·2017-01-19

    Pratt Recalls 2014 ISO Tank Chassis Due to Axle Spindle Defect

    Pratt Industries is recalling 126 units of 2014 DC432LS9 and DC432LS9HL ISO Tank Chassis because a defective axle spindle may cause the wheel end to separate, increasing crash risk.

    Product
    PRATT — PRATT DC432LS9 ISO TANK CHASSIS, DC432LS9HL ISO TANK CHASS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·008-2017·2017-01-19

    Mountain View Packaging Recalls Sweet Chili Chicken Due to Undeclared Allergens

    Mountain View Packaging is recalling 1,080 pounds of sweet chili chicken products because they contain undeclared wheat, egg, and milk allergens.

    Product
    Mountain View Packaging, LLC — Mountain View Packaging, LLC Recalls Chicken Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1129-2017·2017-01-18

    Sabra Hummus Bold & Spicy Recalled for Listeria Contamination Risk

    Sabra Dipping Company is recalling Sabra Hummus Bold & Spicy due to potential Listeria monocytogenes contamination. The product was distributed in the US and three foreign countries.

    Product
    Sabra Hummus Bold & Spicy, 4.56OZ; UPC 040822342506; SKU301430
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1118-2017·2017-01-18

    Sabra Jalapeno Hummus Recalled for Potential Listeria Contamination

    Sabra Dipping Company is recalling 10,498 cases of 10-ounce Jalapeno Hummus due to potential Listeria monocytogenes contamination. The product was distributed in the US and three foreign countries.

    Product
    Sabra Hummus Jalapeno, 10OZ UPC 040822011921, SKU 300106
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1195-2017·2017-01-18

    All American Seasonings Recalls Habanero Ranch Seasoning Due to Salmonella Risk

    All American Seasonings is recalling 69 bags of Habanero Ranch Seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canada.

    Product
    Habanero Ranch Seasoning / Shearer's. Product Code: T4053. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1221-2017·2017-01-18

    Lenny & Larry's Coconut Chocolate Chip Cookies Recalled for Undeclared Milk

    Lenny & Larry's is recalling Coconut Chocolate Chip cookies due to the possible presence of undeclared milk in the dark chocolate chips.

    Product
    4 oz. Complete Cookie, Coconut Chocolate Chip, UPC Code: 7 87692-83538 6, 12pks: 15,834 sleeves (contains 12 cookies) Total cookies from pack sizes above: 190,008
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1121-2017·2017-01-18

    Sabra Recalls Hummus Taco for Potential Listeria Contamination

    Sabra Dipping Company is recalling 10-ounce Hummus Taco products due to potential Listeria monocytogenes contamination. The products were distributed throughout the US and three foreign countries.

    Product
    Sabra Hummus Taco, 10OZ; UPC 040822343671; SKU 301640
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1199-2017·2017-01-18

    All American Seasonings Recalls Nacho Snack Seasoning Due to Salmonella Risk

    All American Seasonings, Inc. is recalling approximately 29 bags of 50 lb Nacho Snack Seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canada.

    Product
    Nacho Snack Seasoning / Harvest Pride /Tom Smith. Product Code: T3809. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1187-2017·2017-01-18

    FONA International Recalls Chai Tea Flavor Due to Salmonella Risk

    FONA International is recalling 300 lbs of N-C Chai Tea Flavor due to possible Salmonella contamination. The product was distributed in Illinois, Wisconsin, New Jersey, Texas, and Canada.

    Product
    N-C Chai Tea Flavor, Nat & Art, NET WEIGHT: 50 LBS, FONA International, Inc., 1900 Averill road, Geneva, IL 60134
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-0875-2017·2017-01-18

    Blue Bell Ice Cream Recalled for Potential Listeria Contamination

    Blue Bell Creameries is recalling specific ice cream products containing cookie dough from Aspen Hills, Inc. due to the potential for Listeria monocytogenes contamination.

    Product
    BLUE BELL(R) ICE CREAM Blue Monster, 3 Gallons
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-1190-2017·2017-01-18

    Valley Milk Products Recalls Sweet Cream Buttermilk Powder for Salmonella Risk

    Valley Milk Products is recalling Sweet Cream Buttermilk Powder in 50-pound bags due to potential Salmonella contamination. The product was distributed to brokers and direct accounts in nine states.

    Product
    Sweet Cream Buttermilk Powder in 50 # bags , manufactured by Valley Milk Products. Stasburg, Virginia 22657 Plant No. 519410 Net Weight - 50 LBS
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-1228-2017·2017-01-18

    St. Clair Pineapple Nut Delight Recalled for Salmonella Risk

    St. Clair Foods is recalling Pineapple Nut Delight because it was made with milk powder potentially contaminated with Salmonella.

    Product
    Pineapple Nut Delight, packaged under the following brands: (a) St. Clair, product code 104003, ST. CLAIR FOODS, INC., NET WT. 5 LBS (2.27 kg), MEMPHIS, TN 38116, UPC 7717114003 (b) Classic SYSCO(R), product code 7166358, NET WT. 5 LBS(2.27 kg), DISTRIBUTED BY SYSCO CORPORATION
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Food)·F-1128-2017·2017-01-18

    Sabra Hummus Lemon Recalled for Potential Listeria Contamination

    Sabra Dipping Company is recalling Sabra Hummus Lemon due to potential Listeria monocytogenes contamination. The product was distributed in the US and three foreign countries.

    Product
    Sabra Hummus Lemon, 10OZ; UPC 040822011648; SKU 301483
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1123-2017·2017-01-18

    Sabra Hummus Recalled for Potential Listeria Contamination

    Sabra Dipping Company is recalling specific lots of Rosemary/Sea Salt Hummus due to potential Listeria monocytogenes contamination.

    Product
    Sabra Hummus SF Rosemary/Sea Salt, 10OZ; UPC 040822342988, SKU 301566
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1116-2017·2017-01-18

    Sabra Recalls Spinach Hummus Due to Listeria Risk

    Sabra Dipping Company is recalling specific sizes of Spinach/Art Hummus because the products have the potential to be contaminated with Listeria monocytogenes.

    Product
    Sabra Hummus Spinach/Art, 10 OZ, 17 OZ, 32OZ UPC SKU ITEM 040822027700 300266 Sabra Hummus Spinach/Art 32OZ 040822027588 300298 Sabra Hummus Spinach/Art 17OZ
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1113-2017·2017-01-18

    Sabra Pine Nut Hummus Recalled for Listeria Contamination Risk

    Sabra Dipping Company is recalling various sizes of Pine Nut Hummus due to potential Listeria monocytogenes contamination. The products were distributed across the US and three foreign countries.

    Product
    Sabra Hummus Pine Nut, 7 OZ, 10 OZ, 17 OZ, 32 OZ UPC SKU ITEM 040822011747 300132 Sabra Hummus Pine Nut 10OZ 040822127530 300134 Sabra Hummus Pine Nut 7OZ 040822990011 300136 Sab
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0876-2017·2017-01-18

    Blue Bell Ice Cream Recalled for Potential Listeria Contamination

    Blue Bell Creameries is recalling four ice cream products containing cookie dough from Aspen Hills, Inc. due to the potential presence of Listeria monocytogenes.

    Product
    BLUE BELL(R) ICE CREAM Krazy Kookie Dough, 3 Gallons
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-1226-2017·2017-01-18

    St. Clair Tropical Fruit Supreme Recalled for Salmonella Risk

    St. Clair Foods is recalling Tropical Fruit Supreme products due to potential salmonella contamination from Valley Milk Dry Milk.

    Product
    Tropical Fruit Supreme, packaged under the following brands: (a) St. Clair, product code 104001, ST. CLAIR FOODS, INC., NET WT. 5 LBS (2.27 kg), MEMPHIS, TN 38116, UPC 7717114001 (b) Classic SYSCO(R), product code 1527001, NET WT. 5 LBS (2.27 kg), DISTRIBUTED BY SYSCO CORPORATIO
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Food)·F-1183-2017·2017-01-18

    FONA International Recalls Butter Flavor Product for Salmonella Contamination

    FONA International is recalling 400 lbs of N-C Butter Flavor Nat WONF due to possible Salmonella contamination. The product was distributed in Illinois, Wisconsin, New Jersey, Texas, and Canada.

    Product
    N-C Butter Flavor Nat WONF, NET WEIGHT: 50 LBS, FONA International, Inc., 1900 Averill road, Geneva, IL 60134
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-0873-2017·2017-01-18

    Blue Bell Ice Cream Recalled for Potential Listeria Contamination

    Blue Bell Creameries is recalling specific ice cream products due to the potential presence of Listeria monocytogenes from a supplier.

    Product
    BLUE BELL(R) ICE CREAM Chocolate Chip Cookie Dough, Half Gallon, Pint, and 3 Gallon sizes.
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-1125-2017·2017-01-18

    Sabra Honey Mustard Spread Recalled for Listeria Contamination Risk

    Sabra Dipping Company is recalling 8.5-ounce jars of Honey Mustard spread due to potential Listeria monocytogenes contamination.

    Product
    Sabra Spreads Honey Mustard, 8.5OZ; UPC 040822343121; SKU301587
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1127-2017·2017-01-18

    Sabra Hummus Basil Pesto Recalled for Listeria Contamination Risk

    Sabra Dipping Company is recalling 10-ounce jars of Hummus Basil-Pesto due to potential Listeria monocytogenes contamination. The product was distributed across the US and three foreign countries.

    Product
    Sabra Hummus Basil-¿Pesto ,10OZ; UPC 040822020114; SKU300593
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1112-2017·2017-01-18

    Sabra Garlic Hummus Recalled for Potential Listeria Contamination

    Sabra Dipping Company is recalling various sizes of Garlic Hummus due to potential Listeria monocytogenes contamination. The product was distributed throughout the US and three foreign countries.

    Product
    Sabra Hummus Garlic, 7 OZ, 10 OZ, 17 OZ, 32 OZ, 30 OZ, 4.56 OZ, 23.5 OZ, UPC SKU ITEM 040822011235 300094 Sabra Hummus Garlic 7OZ 040822011242 300095 Sabra Hummus Garlic 10OZ 040822017510
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1119-2017·2017-01-18

    Sabra Hummus Olive Recalled for Potential Listeria Contamination

    Sabra Dipping Company is recalling 10,094 cases of 10-ounce Sabra Hummus Olive due to potential Listeria monocytogenes contamination.

    Product
    Sabra Hummus Olive, 10OZ; UPC 040822011341; SKU 300117
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1184-2017·2017-01-18

    FONA International Recalls Butter Flavor Product Due to Salmonella Risk

    FONA International is recalling 1,450 pounds of N-C Butter Flavor product due to possible Salmonella contamination. The product was distributed in Illinois, Wisconsin, New Jersey, Texas, and Ontario, Canada.

    Product
    N-C Butter Flv Nat & Art , NET WEIGHT 50 LBS, FONA International, Inc., 1900 Averill road, Geneva, IL 60134
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-1114-2017·2017-01-18

    Sabra Red Pepper Hummus Recalled for Potential Listeria Contamination

    Sabra Dipping Company is recalling multiple sizes of Red Pepper Hummus due to potential Listeria monocytogenes contamination. The product was distributed across the US and three foreign countries.

    Product
    Sabra Hummus Red Pepper, 2 OZ, 4.56 OZ, 5 LB, 7 OZ, 10 OZ, 17 OZ, 30 OZ, 32 OZ UPC SKU ITEM 040822012430 300142 Sabra Hummus Red Pepper 7OZ 040822011549 300143 Sabra Hummus Red Pepper 10OZ 04082201
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0874-2017·2017-01-18

    Blue Bell Ice Cream Recalled for Potential Listeria Contamination

    Blue Bell Creameries is recalling specific ice cream products due to potential Listeria monocytogenes contamination from cookie dough supplied by Aspen Hills, Inc.

    Product
    BLUE BELL(R) ICE CREAM Cookie Two Step, Half Gallon and Pint sizes
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·F-1117-2017·2017-01-18

    Sabra Sun-Dried Tomato Hummus Recalled for Listeria Risk

    Sabra Dipping Company is recalling 10-ounce containers of Sun-Dried Tomato Hummus due to potential Listeria monocytogenes contamination.

    Product
    Sabra Hummus Sun Dried Tomato, 10OZ UPC SKU ITEM 040822014731 300166 Sabra Hummus Sun Dried Tomato 10OZ
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1126-2017·2017-01-18

    Sabra Hummus Recalled for Potential Listeria Contamination

    Sabra Dipping Company is recalling specific lots of 10-ounce Sabra Hummus 3 Pepper Chili due to the potential for Listeria monocytogenes contamination.

    Product
    Sabra Hummus 3 Pepper Chili, 10OZ; UPC 040822344043; SKU301705
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1111-2017·2017-01-18

    Sabra Hummus Classic Recalled for Potential Listeria Contamination

    Sabra Dipping Company is recalling various sizes of Sabra Hummus Classic due to potential Listeria monocytogenes contamination. The product was distributed throughout the US and three foreign countries.

    Product
    Sabra Hummus Classic, 7 OZ, 10 OZ, 17 OZ, 30 OZ, 5 LB, 2 OZ, 4.56 OZ; UPC SKU ITEM 040822000017 300066 Sabra Hummus Classic 7OZ 040822011143 300067 Sabra Hummus Classi
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1202-2017·2017-01-18

    All American Seasonings Recalls OC Ranch French Fry Seasoning Due to Salmonella Risk

    All American Seasonings is recalling specific lots of OC Ranch French Fry Seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canada.

    Product
    OC Ranch French Fry Seasoning/CraftWorks. Product Code: T3996. 12 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1203-2017·2017-01-18

    All American Seasonings Recalls Four Cheese Sauce Mix Due to Salmonella Risk

    All American Seasonings is recalling Four Cheese Sauce Mix drums due to potential Salmonella contamination. The product was distributed nationwide and to Canada.

    Product
    Four Cheese Sauce Mix CR. Product Code: T1729-200. 200/1 lb drums
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1207-2017·2017-01-18

    All American Seasonings Recalls Super Otirod Due to Salmonella Risk

    All American Seasonings, Inc. is recalling 219 bags of Super Otirod seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canada.

    Product
    Super Otirod. Product Code: T3188. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1201-2017·2017-01-18

    All American Seasonings Recalls Broccoli Cheese Soup Due to Salmonella Risk

    All American Seasonings is recalling 13 bags of 50 lb Broccoli Cheese Soup due to potential Salmonella contamination. The product was distributed nationwide and to Canada.

    Product
    Broccoli Cheese Soup / Comfort Foods. Product Code: T3872. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1208-2017·2017-01-18

    Condor Snacks Sour Cream & Onion Seasoning Recalled for Salmonella Risk

    All American Seasonings is recalling 238 bags of Condor Snacks Sour Cream & Onion seasoning due to potential Salmonella contamination.

    Product
    Condor Snacks Sour Cream & Onion W/O MSG. Product Code: T3235. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1251-2017·2017-01-18

    Po Folks Cornbread Mix Recalled for Possible Salmonella Contamination

    House-Autry Mills is recalling Po Folks Cornbread Mix because it contains milk product from a supplier recalling for possible Salmonella presence.

    Product
    Po Folks Cornbread Mix, Net Wt., 5 lb bags, UPC Code 0 73484 22509 2
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-1209-2017·2017-01-18

    All American Seasonings Recalls Spicy Nacho Seasoning Due to Salmonella Risk

    All American Seasonings, Inc. is recalling 211 bags of 50 lb Spicy Nacho seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canadian consignees.

    Product
    Spicy Nacho. Product Code: T3552. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide

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