The Recall Desk

Archive

October 2019 recalls

807 recalls were announced in October 2019.

What the numbers show

Critical
64
Severe
328
High
307
Moderate
88
Low
20

Of the 807 recalls this month scored against our rubric, 8% are Critical, 41% are Severe.

101–200 of 807

  • SevereNHTSA·19V767000·2019-10-25

    Ford Recalls 2015-2017 Transit Vehicles for Driveshaft Coupling Failure

    Ford is recalling 2015-2017 Transit vehicles because the flexible coupling connecting the transmission to the driveshaft may prematurely fail, potentially causing loss of power or vehicle movement.

    Product
    FORD — FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V766000·2019-10-25

    Ford Recalls 2019 Edge Vehicles Due to Seat Belt Anchor Defect

    Ford is recalling 2019 Edge vehicles because the driver-side seat belt pretensioner anchor may be improperly crimped, risking webbing detachment in a crash.

    Product
    FORD — FORD EDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V765000·2019-10-25

    Blue Bird Recalls 2018-2019 School Buses Due to Software Error

    Blue Bird is recalling 2018-2019 Vision and All American school buses because a software error may cause unexpected vehicle movement.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN, VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V772000·2019-10-25

    Forest River Recalls 2020 Surveyor Trailers Due to Fire Risk

    Forest River is recalling 2020 Surveyor trailers because an incorrect fuse may allow wiring to overheat, increasing the risk of fire.

    Product
    FOREST RIVER — FOREST RIVER SURVEYOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·103-2019·2019-10-25

    Taylor's Sausage Recalls Ready-to-Eat Products Due to Undeclared Casings

    Taylor's Sausage Inc. is recalling approximately 1,086 pounds of ready-to-eat meat and poultry products because they may contain undeclared pork or sheep casings.

    Product
    Taylor's Sausage, Inc. — Taylor’s Sausage Inc. Recalls Ready-To-Eat Meat and Poultry Products Due to Mislabeling
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·19V761000·2019-10-24

    GM Recalls 2014-2020 Trucks and SUVs for Braking Software Defect

    General Motors is recalling specific 2014-2020 Chevrolet and GMC vehicles because a software defect may cause unintended braking and vehicle pulling.

    Product
    GMC — GMC, CHEVROLET YUKON, TAHOE, SUBURBAN, SILVERADO 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V756000·2019-10-24

    Volvo Recalls 2020 VNL and VNR Trucks for Steering Gear Defect

    Volvo Trucks is recalling 2,287 2020 VNL and VNR trucks because steering gear fasteners may be loose, risking loss of vehicle control.

    Product
    VOLVO — VOLVO VNR, VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V758000·2019-10-24

    Dodge Charger and Challenger Recall for Front Wheel and Brake Defect

    FCA US is recalling 2019 Dodge Charger and Challenger vehicles because an incompatible front wheel and brake package may allow the front tire to contact the steering knuckle, causing tire damage.

    Product
    DODGE — DODGE CHARGER, CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V757000·2019-10-24

    Ram 1500 Recall: EGR Cooler Crack May Cause Intake Manifold Fire

    Chrysler is recalling 2014-2019 Ram 1500 trucks with 3.0L Eco Diesel engines because a cracked EGR cooler may allow coolant vapor to combust, increasing fire risk.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V759000·2019-10-24

    Dodge Grand Caravan Recall for Rear Seat Striker Weld Defects

    FCA US LLC is recalling 2019 Dodge Grand Caravan vehicles because seat striker welds may fail in crashes, increasing injury risk.

    Product
    DODGE — DODGE GRAND CARAVAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V762000·2019-10-24

    GM Recalls 2019-2020 Buick Regal for Front Seat Weld Defect

    General Motors is recalling 2019-2020 Buick Regal vehicles because improperly welded front seat frames may not provide adequate crash protection, increasing injury risk.

    Product
    BUICK — BUICK REGAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V760000·2019-10-24

    Southern Pride Recalls 2019 Lakeline Rail Trailers Due to Short Safety Chains

    Southern Pride is recalling 2019 Lakeline Rail trailers because safety chains may be too short to attach to the tow vehicle, increasing the risk of detachment and a crash.

    Product
    SOUTHERN PRIDE — SOUTHERN PRIDE LAKELINE RAIL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0111-2020·2019-10-23

    E.A. Sween Recalls Ranch Chicken Salad Croissants for Listeria Risk

    E.A. Sween Co. is recalling Market Sandwich Ranch chicken Salad on a Croissant nationwide due to potential Listeria monocytogenes contamination.

    Product
    Market Sandwich Ranch chicken Salad on a Croissant. Net Wt. 6.8 oz. (193g) UPC 41433-02351. Keep Refrigerated. EA Sween Company, Eden Prairie, MN 55344.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0112-2020·2019-10-23

    E.A. Sween Recalls Archer Farms Turkey and Havarti Sandwiches

    E.A. Sween Co. is recalling Archer Farms Turkey & Havarti sandwiches due to potential Listeria monocytogenes contamination.

    Product
    archer farms Turkey & Havarti sandwich on wheat bread Net Wt 5.7 oz (162g) Perishable / Keep Refrigerated. UPC: 85239-03283 Dist By Target Corporation, Minneapolis, MN 55403.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0048-2020·2019-10-23

    Lyons Magnus Recalls Dunkin' Mocha Swirl for Undeclared Milk

    Lyons Magnus, Inc. is recalling Dunkin' Mocha Swirl because the product was mislabeled and contains undeclared milk.

    Product
    Dunkin' Mocha Swirl Prepared Exclusively for Dunkin' Brands Canton, MA 02021 Net Contents 64 FL OZ/1.89L Not For Resale
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0115-2020·2019-10-23

    E.A. Sween Recalls Tuna Salad Sandwiches for Listeria Risk

    E.A. Sween Co. is recalling Market Sandwich Artisan Style Albacore Tuna Salad on Dark Wheat Bread nationwide due to potential Listeria monocytogenes contamination.

    Product
    Market Sandwich Artisan Style Albacore Tuna Salad on Dark Wheat Bread, Keep Refrigerated. Net Wt 7.8 oz (221g)UPC 41433-02845 E.A. Sween Company, Eden Prairie MN 55344
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0109-2020·2019-10-23

    E.A. Sween Recalls Dill Egg Salad Sandwiches for Listeria Risk

    E.A. Sween Co. is recalling Market Sandwich Dill Egg Salad products nationwide due to potential Listeria monocytogenes contamination.

    Product
    Market Sandwich Dill Egg Salad on Classic White Bread, Net Wt. 5.0 oz. (142g) UPC: 41433-02669 Keep Refrigerated. Deli Express, Eden Prairie, MN 55344.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0113-2020·2019-10-23

    Recall of Deli Express Tuna Salad Sandwiches Due to Listeria Contamination

    Various sandwiches, including Deli Express Tuna Salad on Cracked Wheat Bread, are recalled because they may contain Listeria monocytogenes, a high-risk pathogen.

    Product
    Deli Express Tuna Salad on Cracked Wheat Bread, Net Wt 5.0 oz (142g) UPC 41433-02121 EA Sween Company Eden Prairie MN 55344.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0103-2020·2019-10-23

    E.A. Sween Recalls Chicken Salad Sandwiches for Listeria Risk

    E.A. Sween Co. is recalling Speedy good to go Chicken Salad on Wheat Bread sandwiches nationwide due to potential Listeria monocytogenes contamination.

    Product
    Speedy good to go Chicken Salad on Wheat Bread. Net Wt 4.7oz. (133g) UPC 41112-10289. Keep Refrigerated. Manufactured for Speedway LLC, 500 Speedway Dr. Enon, OH 45323
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0102-2020·2019-10-23

    E.A. Sween Recalls Chicken Salad Sandwiches for Listeria Risk

    E.A. Sween Co. is recalling chicken salad sandwiches due to potential Listeria monocytogenes contamination. The recall covers nationwide distribution.

    Product
    Chicken Salad on White Bread Sandwich, Net Wt. 5 oz. 142g), packaged as follows: 1. Deli Express, Keep Refrigerated, UPC 41433-02118, EA Sween Company, Eden Prairie, MN 55344 2. K&G, UPC 08615-35576. Distributed By: Kum & Go L.C. West Des Moines, IA 50266.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0106-2020·2019-10-23

    E.A. Sween Recalls Cranberry Almond Chicken Sandwiches for Listeria Risk

    E.A. Sween Co. is recalling Mega Cranberry Almond Chicken Salad sandwiches nationwide due to potential Listeria monocytogenes contamination.

    Product
    Mega Cranberry Almond Chicken Salad on Stone Ground Wheat Bread. Net Wt. 7.8oz. (221g). Keep Refrigerated. Packaged under the following Labels: 1. Market Sandwich Artisan Style UPC: 41433-02670 Deli Express, Eden Prairie, MN 55344. 2. Speedy good to go UPC: 41112-1
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0104-2020·2019-10-23

    E.A. Sween Recalls Ranch Chicken Salad Sandwiches for Listeria Risk

    E.A. Sween Co. is recalling Market Sandwich Ranch Chicken Salad on White Bread nationwide due to potential Listeria monocytogenes contamination.

    Product
    Market Sandwich Ranch Chicken Salad on White Bread Net Wt. 5.0 oz. (142g) UPC: 41433-00953. Keep Refrigerated. Deli Express Eden Prairie, MN 55344
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0050-2020·2019-10-23

    Massey Fish Company Smoked Whitefish Pate Recalled for Listeria

    Massey Fish Company is recalling Smoked Whitefish Pate because samples tested positive for Listeria monocytogenes. The product was distributed in Michigan.

    Product
    Massey Fish Company Smoked Whitefish Pate, in a refrigerated 8 oz. plastic tub, with UPC number 854656007018
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·19V754000·2019-10-23

    Forest River Recalls 2020 Travel Trailers Due to Fire Risk

    Forest River is recalling 2020 EVO, Salem, and Wildwood travel trailers because rubber propane gas lines may melt and cause a fire.

    Product
    FOREST RIVER — FOREST RIVER WILDWOOD, SALEM, STEALTH EVO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0107-2020·2019-10-23

    E.A. Sween Recalls Archer Farms Chicken Salad Sandwiches for Listeria Risk

    E.A. Sween Co. is recalling Archer Farms Cranberry Almond Chicken Salad sandwiches due to potential Listeria monocytogenes contamination.

    Product
    archer farms Cranberry Almond Chicken Salad sandwich on cranberry wild rice Bread. Net Wt. 5.7oz. (162g). UPC: 85239-03284. Perishable Keep Refrigerated. Dist. by Target Corporation, Minneapolis, MN 55403
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0093-2020·2019-10-23

    Northern Fisheries Recalls Frozen Raw Tuna Loins Due to Scombroid Poisoning Complaints

    Northern Fisheries Ltd. is recalling frozen raw tuna loins after customers reported consumer complaints of scombroid poisoning symptoms.

    Product
    Frozen, raw tuna loins packed in vacuum packages weighing between 5-8 Lbs. each. Packed in cardboard cases (30 Lbs. per case).
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-0110-2020·2019-10-23

    E.A. Sween Recalls Market Sandwich Everything Bagels for Listeria Risk

    E.A. Sween Co. is recalling Market Sandwich Everything Bagels with smoked meats and cheese due to potential Listeria monocytogenes contamination.

    Product
    Market Sandwich Everything Bagel with Smoked Ham, Smoked White Turkey, Swiss Cheese & Garlic Dijon Aioli. Net Wt. 7.1 oz. (201g) Keep Refrigerated. UPC 41433-02813. EA Sween Company, Eden Prairie, MN 55344.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0132-2020·2019-10-23

    ICU Medical Recalls Sapphire Infusion Sets Due to Potential Fluid Leakage

    ICU Medical is recalling Sapphire Epidural Infusion Sets because fluid may leak from the inline filter air vents. The recall covers 26,700 units distributed nationwide and internationally.

    Product
    Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Epidural Set Yellow-Striped Microbore, 0.2 Micron Filter, PAV 123 inch. 1 unit per pouch; 50 pouches per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0144-2020·2019-10-23

    ICU Medical Recalls Sapphire Infusion Sets Due to Fluid Leakage Risk

    ICU Medical Inc is recalling Sapphire Microbore Infusion Sets with inline filters because they may leak fluid from air vents. The affected units were distributed nationwide and internationally.

    Product
    Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Epidural Set Yellow-Striped Microbore, 0.2 Micron Filter 301 cm / 8.3 mL. 1 unit per blister; 40 blisters per case . Not distributed in the U.S.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V755000·2019-10-23

    BMW Recalls 2020 330i and M340i for Trunk Release Cable Defect

    BMW is recalling 2020 330i and M340i vehicles because an improperly installed trunk release cable may prevent the trunk from opening from the inside.

    Product
    BMW — BMW 330I, M340I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0124-2020·2019-10-23

    Integra LifeSciences Recalls Cerelink ICP Monitor Due to Reading Decline

    Integra LifeSciences is recalling 189 Cerelink ICP Monitor units because they may show a progressive decline in intracranial pressure readings during use.

    Product
    Cerelink ICP Monitor, Model Number 826820; intended for use as an interface between compatible strain-gauge type pressure transducers and standard physiological pressure monitoring systems.
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Food)·F-0108-2020·2019-10-23

    Recall of Deli Express Egg Salad Sandwiches Due to Potential Listeria Contamination

    The FDA is recalling Deli Express Egg Salad on Homestyle White Bread because various sandwiches may be contaminated with Listeria monocytogenes, posing a food safety risk.

    Product
    Deli Express Egg Salad on Homestyle White Bread, Net Wt. 4.8 oz. (136g) UPC: 41433-02123, E.A. Sween Company, Eden Prairie, MN 55344.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0127-2020·2019-10-23

    ICU Medical Recalls Plum Microbore Infusion Sets Due to Fluid Leakage

    ICU Medical Inc is recalling specific Plum Microbore Infusion Sets because fluid may leak from the inline filter air vents.

    Product
    Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as Primary PLUM Set 0.2 Micron Filter, Prepierced Y-Site, Polyethylene Lined Light Resistant Tubing, Distal Microbore Tubing, Secure Lock, 104 Inch. 1 unit per pouch; 50 po
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0142-2020·2019-10-23

    ICU Medical Recalls Sapphire Infusion Sets Due to Fluid Leakage Risk

    ICU Medical is recalling Sapphire Microbore Infusion Sets with inline filters due to a potential for fluid leakage out of air vents.

    Product
    Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Primary 0.2 Micron Filter Set Non-Vented, Microbore, 293 cm / 8.1 mL. 1 unit per pouch; 1 unit per blister; 40 blisters per case. Not distributed in the U.S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0133-2020·2019-10-23

    ICU Medical Recalls Sapphire Infusion Sets Due to Potential Fluid Leakage

    ICU Medical Inc is recalling Sapphire Microbore Infusion Sets because fluid may leak from the inline filter air vents.

    Product
    Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Primary 0.2 Micron Filter Set Non-Vented, Microbore, PAV, CLAVE Y-Site, 122 Inch. 1 unit per pouch; 50 pouches per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0134-2020·2019-10-23

    ICU Medical Recalls Sapphire Infusion Sets Due to Fluid Leakage Risk

    ICU Medical is recalling Sapphire Microbore Infusion Sets because fluid may leak from the inline filters. The recall covers 19,350 units distributed nationwide and internationally.

    Product
    Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Primary 1.2 Micron Filter Set Non-Vented, Microbore, PAV, 123 Inch. 1 unit per pouch; 50 pouches per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0139-2020·2019-10-23

    ICU Medical Recalls Plum Microbore Infusion Sets Due to Fluid Leakage Risk

    ICU Medical Inc is recalling 521 units of Plum Microbore Infusion Sets because air vents on inline filters may leak fluid. The recall covers nationwide and international distribution.

    Product
    Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as Primary PLUM Set, 15 Micron Filter in Sight Chamber, CLAVE Secondary Port, 0.2 Micron Filter, Polyethylene Lined Light Resistant Tubing, Distal Microbore Tubing, Secure Loc
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0051-2020·2019-10-23

    Jansal Valley Snack Mix Recalled for Incorrect Allergen Labeling

    Friendly Fruit Market is recalling Jansal Valley Indulgent Snack Mix because the label lists allergens not actually in the product.

    Product
    Jansal Valley brand Indulgent Snack Mix NET WT 12 OZ (340 G) in plastic clamshells, Ingredients: apricots, almonds, banana chips, coconut, cashews, dates, raisins, hazelnuts, pecans, pepitas, walnuts, papaya, pineapple. Contains: almonds, cashews, soy. This product is packaged in
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-0053-2020·2019-10-23

    Foremost Foods Recalls Frozen Yellow Tail Due to Salmonella

    Foremost Foods International is recalling 43 cases of Frozen Whole Yellow Tail Fusiler-200 Up because the product was mistakenly distributed to a retail supermarket with Salmonella.

    Product
    Frozen Whole Yellow Tail Fusiler-200 Up
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0135-2020·2019-10-23

    ICU Medical Recalls Sapphire Infusion Sets Due to Fluid Leakage Risk

    ICU Medical is recalling Sapphire Microbore Infusion Sets because fluid may leak from the inline filters. The recall covers 4,600 units distributed nationwide and internationally.

    Product
    Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Epidural Set with NRFit Connector Yellow-Striped Microbore, 0.2 Micron Filter 119 Inch. 1 unit per pouch; 50 pouches per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0143-2020·2019-10-23

    ICU Medical Recalls Sapphire Microbore Infusion Sets Due to Leakage Risk

    ICU Medical is recalling Sapphire Microbore Infusion Sets because fluid may leak from the inline filter air vents. The product was distributed in the U.S. and internationally.

    Product
    Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Epidural Set Yellow-Striped Microbore, 0.2 Micron Filter 301 cm / 8.3 mL. 1 unit per blister; 40 blisters per case . Not distributed in the U.S.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0148-2020·2019-10-23

    Siemens Atellica CH 930 Analyzer Recalled for Erroneous Hemolysis and Lipemia Indices

    Siemens Healthcare Diagnostics is recalling 1,125 Atellica CH 930 Analyzers worldwide due to software errors that may produce incorrect hemolysis and lipemia indices.

    Product
    Siemens Atellica CH 930 Analyzer. Siemens Material Number (SMN): 11067000 Product Usage: automated, clinical chemistry analyzer to perform in vitro diagnostic tests on clinical specimens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0129-2020·2019-10-23

    ICU Medical Recalls Sapphire Infusion Sets Due to Fluid Leakage Risk

    ICU Medical is recalling Sapphire Microbore Infusion Sets because fluid may leak from the inline filter air vents.

    Product
    Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Primary 1.2 Micron Filter Set Microbore, 122 Inch. 1 unit per pouch; 50 pouches per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0147-2020·2019-10-23

    ICU Medical Recalls Sapphire Infusion Sets Due to Fluid Leakage Risk

    ICU Medical is recalling Sapphire Microbore Infusion Sets because fluid may leak from the inline filters. The recall covers units distributed nationwide and internationally.

    Product
    Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Epidural Set with NRFit Connector Yellow-Striped Microbore, 0.2 Micron Filter, PAV, 123 Inch. 1 unit per pouch; 50 pouches per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0114-2020·2019-10-23

    Tuna Salad on Wheat Bread sandwiches may contain Listeria monocytogenes contaminant

    FDA is recalling various tuna salad on wheat bread sandwiches due to potential Listeria monocytogenes contamination. Consumers should discard affected products to prevent possible illness.

    Product
    Tuna Salad on Wheat Bread, Keep Refrigerated. packaged under the following: 1. Market Sandwich Albacore Net Wt 5.0 oz (142g)UPC 41433-00954 Deli Express, Eden Prairie MN 55344. 2. Speedy good to go, Net Wt 4.7 oz (133g), UPC 41112-10288 Manufactured for: Speedway L
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0145-2020·2019-10-23

    ICU Medical Recalls Plum Microbore Infusion Sets Due to Leakage Risk

    ICU Medical Inc is recalling 7,920 units of Plum Microbore Infusion Sets because fluid may leak from the inline filters.

    Product
    Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as PLUM Epidural Set with NRFit Connector Yellow-Striped Tubing, Distal Microbore Tubing, 0.2 Micron Filter, 107 Inch. 1 unit per pouch; 48 pouches per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0159-2020·2019-10-23

    Olympus Berkeley Disposa-Filter Recall Due to Weld Defect

    Olympus is recalling Berkeley Disposa-Filters used with the VC-10 Vacuum Curettage System because an ultrasonic weld defect may cause the housing to separate.

    Product
    Berkeley Disposa-Filter used with Berkeley VC-10 Vacuum Curettage System - Product Usage: designed for rapid transcervical aspiration of the uterine cavity. Part# 54298-10/pack
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0151-2020·2019-10-23

    Xodus Medical Recalls Cautery Tip Cleaners Due to Sterile Barrier Concerns

    Xodus Medical Inc is recalling 255,000 Cautery Tip Cleaners because the sterile barrier of some devices may have been affected.

    Product
    Cautery Tip Cleaner REF: 30500 Product Usage: electrosurgical accessory
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0052-2020·2019-10-23

    Jansal Valley Snack Mix Recalled for Incorrect Allergen Labeling

    Friendly Fruit Market is recalling Jansal Valley Energize Snack Mix because the label lists allergens that are not actually in the product.

    Product
    Jansal Valley brand Energize Snack Mix NET WT 5 OZ (142 G) in plastic clamshells, Ingredients: apricots, almonds, banana chips, coconut, cashews, dates, raisins, hazelnuts, pecans, pepitas, walnuts, papaya, pineapple. Contains: almonds, cashews, coconut, hazelnuts, pecans, walnut
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-0122-2020·2019-10-23

    Medtronic Euphoria Balloon Catheters Recalled for Stylette Removal Difficulties

    Medtronic is recalling Euphoria Rapid Exchange Balloon Dilatation Catheters because a slightly higher diameter stylette causes removal difficulties.

    Product
    Euphoria Rapid Exchange Balloon Dilatation Catheter, Product Numbers: EUP1506X, EUP1510X, EUP1512X, EUP1515X, EUP1520X, EUP2006X, EUP2010X, EUP2012X, EUP2015X, EUP2020X, EUP2025X, EUP2030X, EUP22506X, EUP22510X, EUP22512X, EUP22515X, EUP22520X, EUP22525X, EUP2506X, EUP2510X, EUP
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0128-2020·2019-10-23

    ICU Medical Recalls Plum Microbore Infusion Sets Due to Leakage Risk

    ICU Medical is recalling specific Plum Microbore Infusion Sets because fluid may leak from the inline filter air vents.

    Product
    Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as Primary PLUM Set Yellow Striped Tubing, Distal Microbore Tubing, 0.2 Micron Filter, Secure Lock, 107 Inch. 1 unit per pouch; 48 pouches per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0131-2020·2019-10-23

    ICU Medical Recalls Sapphire Infusion Sets Due to Fluid Leakage Risk

    ICU Medical is recalling Sapphire Microbore Infusion Sets because fluid may leak from the inline filter air vents.

    Product
    Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Epidural Set Yellow-Striped Microbore, 0.2 Micron Filter 119 Inch. 1 unit per pouch; 50 pouches per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0036-2020·2019-10-23

    Gullah Gourmet Recalls Nana's Been a Nut Bread for Missing Walnut Labeling

    Gullah Gourmet, Inc. is recalling 673 bags of Nana's Been a Nut Bread because the ingredient statement does not list walnuts, posing a risk to consumers with walnut allergies.

    Product
    Nana's Been a Nut Bread NET WT. 11oz/311.74g cloth bag CONTAINS WHEAT AND SOY. MADE ON EQUIPMENT THAT MAKES PRODUCTS CONTAINING WHEAT, EGGS, MILK, SOY AND TREE NUTS. GULLAH BOURMET Inc. CHARLESTON, SC 29407 UPC 6 50305 01045 9
    Category
    Food
    Distribution
    16 states
  • HighFDA (Food)·F-0105-2020·2019-10-23

    Market Sandwich Artisan Style Ranch Chicken Salad sandwiches may contain Listeria monocytogenes.

    A recall has been issued for Market Sandwich Artisan Style Ranch Chicken Salad sandwiches due to potential Listeria monocytogenes contamination. The manufacturer E.A. Sween Co. is recalling these products nationwide.

    Product
    Market Sandwich Artisan Style Ranch Chicken Salad sandwich, Oat Topped Dark Wheat Bread, Net Wt. 7.8 oz. (221g) UPC: 41433-02458. E.A. Sween Company, Eden Prairie, MN 55344.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0137-2020·2019-10-23

    ICU Medical Recalls Plum Microbore Infusion Sets Due to Fluid Leakage Risk

    ICU Medical Inc is recalling specific Plum Microbore Infusion Sets because fluid may leak from the inline filters. The affected units were distributed nationwide and internationally.

    Product
    Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as Primary PLUM Set 15 Micron Filter in Sight Chamber, CLAVE Secondary Port, 0.2 Micron Filter, CLAVE Y-Site, Polyethylene Lined Light Resistant Tubing, Distal Microbore Tubin
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0157-2020·2019-10-23

    Vital Scientific Selectra ProM Analyzer Recalled for Power Supply Failure

    Vital Scientific N.V. is recalling five Selectra ProM Analyzers due to power supply failures that cause instrument malfunction and prevent the production of patient results.

    Product
    Selectra ProM Analyzer, Catalog # 6003-435/UDI # 03661540600395 and Catalog # 6003-436/UDI # 03661540600401 Product Usage: :clinical chemistry system intended for use in clinical laboratories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0141-2020·2019-10-23

    ICU Medical Recalls Sapphire Infusion Sets Due to Fluid Leakage Risk

    ICU Medical is recalling Sapphire Microbore Infusion Sets with inline filters due to a potential for fluid leakage out of air vents.

    Product
    Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Primary 1.2 Micron Filter Set Non-Vented, Microbore 311 cm / 8.4 mL. 1 unit per pouch; 1 unit per blister; 40 blisters per case . Not distributed in the U.S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0141-2020·2019-10-23

    Spectrum Chemical Recalls Fentanyl Citrate Due to Glass Contamination

    Spectrum Laboratory Products is recalling Fentanyl Citrate USP active pharmaceutical ingredient due to potential glass contamination. The product was distributed to compounding pharmacies and labs in four states.

    Product
    Fentanyl Citrate USP, Active Pharmaceutical Ingredient, Spectrum Chemical MFG. CORP., Gardena, CA 90248 NDC 49452-0032-06
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Devices)·Z-0136-2020·2019-10-23

    ICU Medical Recalls Plum Microbore Infusion Sets Due to Leakage Risk

    ICU Medical is recalling specific Plum Microbore Infusion Sets because fluid may leak from the inline filters. The affected units were distributed nationwide and internationally.

    Product
    Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as PRIMARY PLUMSET 15 Micron Filter in Sight Chamber, CLAVE Port, 0.2 Micron Filter, CLAVE Y-Site, PE Lined Light Resistant Tubing, Distal Microbore Tubing 272 cm / 15 mL. 1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0060-2020·2019-10-23

    G&C Food Distributors Recalls Frozen Blackberries Due to Norovirus Contamination

    G&C Food Distributors is recalling 299 cases of frozen blackberries because the product is contaminated with norovirus. The affected bags were distributed to retailers in nine states and Belize.

    Product
    Frozen blackberries, packaged in 16 ounce (454 gram) plastic bags (12 bags per master case). Plastic bags labeled with: PREMIUM QUALITY, KEEP FROZEN, NON-GMO, CORNERSTONE PREMIUM FOODS, Blackberries, GREAT FOR SMOOTHIES, NET WEIGHT 16 OZ. (454g), INGREDIENTS: BLACKBERRIES, GC
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-0126-2020·2019-10-23

    ICU Medical Recalls Plum Microbore Infusion Sets Due to Leakage Risk

    ICU Medical is recalling specific Plum Microbore Infusion Sets because fluid may leak from the inline filter air vents. The recall covers 170,735 units distributed nationwide and internationally.

    Product
    Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as High-Pressure Filter PRIMARY I.V. PLUMSET Convetible Pin, 104 Inch with Orange Polyethylene-Lined*/Light Resistant Tubing, Prepierced Injection Site and OPTION-LOK. 1 uni
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0130-2020·2019-10-23

    ICU Medical Recalls Sapphire Infusion Sets Due to Fluid Leakage Risk

    ICU Medical is recalling Sapphire Microbore Infusion Sets with inline filters because fluid may leak out of the air vents. The recall covers 45,900 units distributed nationwide and internationally.

    Product
    Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Primary 0.2 Micron Filter Set, Microbore, CLAVE Y-Site, 118 Inch. 1 unit per pouch; 50 pouches per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0150-2020·2019-10-23

    Xodus Medical Recalls Electrosurgical Tip Cleaners Due to Sterile Barrier Concerns

    Xodus Medical Inc is recalling 460,000 Electrosurgical Tip Cleaners because the sterile barrier of some devices may have been affected.

    Product
    Electrosurgical Tip Cleaner REF: 62-8499-001 Product Usage: electrosurgical accessory
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0146-2020·2019-10-23

    ICU Medical Recalls Sapphire Infusion Sets Due to Fluid Leakage Risk

    ICU Medical Inc is recalling Sapphire Microbore Infusion Sets with Inline Filters due to a potential for fluid leakage out of air vents.

    Product
    Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Epidural Set with NRFit Connector Yellow-Striped Microbore, 0.2 Micron Filter 301 cm / 8.3 mL. 1 unit per blister; 40 blisters per case. Not distributed in t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0125-2020·2019-10-23

    OrthoPediatrics Recalls Adolescent Attachment Bolts Due to Interference Risk

    OrthoPediatrics Corp is recalling 211 units of Adolescent attachment bolts used with the Pediatric Nailing Platform. The recall is due to potential interference between the bolt and nail, which may delay surgical procedures.

    Product
    OrthoPediatrics Adolescent attachment bolt used with the Pediatric Nailing Platform (PNP) targeting arm- intended as an orthopedic implant system (bolt is used to attach the targeting arm to the intramedullary fixation rod) Part number: 01-1503-0032
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0140-2020·2019-10-23

    ICU Medical Recalls Sapphire Infusion Sets Due to Fluid Leakage Risk

    ICU Medical Inc is recalling Sapphire Microbore Infusion Sets with Inline Filters due to a potential for fluid leakage out of air vents.

    Product
    Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Primary 1.2 Micron Filter Set Non-Vented, Microbore 311 cm / 8.4 mL. 1 unit per pouch; 1 unit per blister; 40 blisters per case . Not distributed in the U.S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0138-2020·2019-10-23

    ICU Medical Recalls Plum Microbore Infusion Sets Due to Leakage Risk

    ICU Medical is recalling specific Plum Microbore Infusion Sets because fluid may leak from the inline filter air vents. The recall covers 6,400 units distributed in the U.S. and internationally.

    Product
    Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as Primary PLUM Set 15 Micron Filter in Sight Chamber, CLAVE Secondary Port, 0.2 Micron Filter, CLAVE Y-Site, Polyethylene Lined Light Resistant Tubing, Distal Microbore Tubin
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0154-2020·2019-10-23

    Vital Scientific Viva-JR Automated Chemistry Analyzer Recalled for Power Supply Failure

    Vital Scientific N.V. is recalling four Viva-JR automated chemistry analyzers due to power supply failures that cause instrument malfunction and prevent the production of patient results.

    Product
    Viva - JR, catalog # 6002-940, UDI # 03661540600210 Product Usage: automated chemistry analyzer intended for clinical use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0123-2020·2019-10-23

    Medtronic Solarice Balloon Catheter Recall Due to Stylette Removal Difficulty

    Medtronic is recalling Solarice Rapid Exchange Balloon Dilatation Catheters because a slightly higher diameter stylette may cause removal difficulties.

    Product
    Solarice Rapid Exchange Balloon Dilatation Catheter, Product Numbers: SLC1506X, SLC1510X, SLC1512X, SLC1515X, SLC1520X, SLC2006X, SLC2010X, SLC2012X, SLC2015X, SLC2020X, SLC2025X, SLC2030X, SLC22510X, SLC22515X, SLC22520X, SLC22525X, SLC2506X, SLC2510X, SLC2512X, SLC2515X, SLC25
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Food)·F-0041-2020·2019-10-23

    CTC Food International Recalls Orchids Dried Mushroom for Undeclared Sulfites

    CTC Food International is recalling Orchids Dried Mushroom because it contains undeclared sulfites. The recall covers 28,800 units distributed to eight U.S. states.

    Product
    Orchids Dried Mushroom NET WT. 1 oz. (29G) Product of China UPC 0-74601-00947-2 Distributed by CTC Food International, Inc. Richmond, CA 94804
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-0156-2020·2019-10-23

    Vital Scientific V-Twin Automated Chemistry Analyzer Recalled for Power Supply Failure

    Vital Scientific N.V. is recalling 39 V-Twin automated chemistry analyzers due to a power supply failure that prevents the instruments from producing patient results.

    Product
    V-Twin, Catalog # 6002-800, UDI # 03661540600180 Product Usage: automated chemistry analyzer intended for clinical use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0143-2020·2019-10-23

    Aurobindo Recalls Amphetamine Mixed Salts Tablets for Out-of-Specification Weight

    Aurobindo Pharma USA Inc. is recalling 11,129 bottles of 20mg Amphetamine Mixed Salts tablets because they failed weight and thickness specifications.

    Product
    DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE — DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0049-2020·2019-10-23

    Climax Spring Water Recalled for Excessive Bromate Levels

    King Bottling, Inc. is recalling Climax Spring Water in various sizes because it contains bromate levels above the FDA standard of quality limit.

    Product
    Climax Spring Water bottled in 5 gallon, 1 gallon, and 16.9 ounce plastic bottles (12 bottles per case)
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0145-2020·2019-10-23

    Jubilant Cadista Recalls Pantoprazole Sodium Tablets Due to Discoloration

    Jubilant Cadista Pharmaceuticals is recalling specific lots of Pantoprazole Sodium Delayed Release Tablets due to dark brown discoloration on tablet edges.

    Product
    Pantoprazole Sodium Delayed Release Tablets, USP, 40 mg, packaged in 90-count bottle, Rx only, Manufactured by: Jubilant Generics Ltd, Roorkee - 247661, India, Marketed by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, NDC 59746-284-90
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-0158-2020·2019-10-23

    Vital Scientific Selectra ProS Analyzer Recalled for Power Supply Failure

    Vital Scientific is recalling six Selectra ProS Analyzers due to power supply failures that cause instrument malfunction and prevent the production of patient results.

    Product
    Selectra ProS Analyzer, Catalog # 6003-600/UDI # 03661540600418 Product Usage: :clinical chemistry system intended for use in clinical laboratories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0146-2020·2019-10-23

    Ingenus Recalls Leucovorin Calcium Injection Due to Crystallization

    Ingenus Pharmaceuticals is recalling Leucovorin Calcium Injection vials due to the presence of particulate matter identified as API crystallization.

    Product
    Leucovorin Calcium Injection, USP 500 mg*/50 mL (10 mg/mL) 50 mL Single-Dose Vial NDC 50742-464-50 Rx Only Ingenus Pharmaceuticals, LLC. Orlando, FL 32839
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0144-2020·2019-10-23

    Atlas Pharmaceuticals Recalls Ascorbic Acid Injection Due to Corn Source Labeling Error

    Atlas Pharmaceuticals is recalling Ascorbic Acid Sterile Injection Solution vials labeled as 'Non-Corn Source' but actually derived from corn. The recall affects 1,646 vials distributed to healthcare facilities in Arizona and Colorado.

    Product
    Ascorbic Acid Sterile Injection Solution, 500 mg/mL, 50 mL vial, Non-Corn Source, Rx only, Atlas Pharmaceuticals, LLC, 711 E Carefree Hwy, Suite 107, Phoenix, AZ 85085, NDC 71591-500-50.
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Food)·F-0035-2020·2019-10-23

    Arcadia Trading Recalls Dried Mushroom Bags for Undeclared Sulfites

    Arcadia Trading Inc. is recalling 1,425 bags of dried mushrooms because they contain undeclared sulfites. The product was distributed to a New York distributor and further distributed in seven states.

    Product
    Dried Mushroom NET WT: 8oz (227g) Ingredients: Mushroom Distributed By: Arcadia Trading Inc. Brooklyn, NY 11211. USA Product of China UPC: 791804603091
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-0155-2020·2019-10-23

    Vital Scientific Viva-E Automated Chemistry Analyzer Recalled for Power Supply Failure

    Vital Scientific N.V. is recalling 75 Viva-E automated chemistry analyzers due to power supply failures that prevent the instruments from producing patient results.

    Product
    Viva-E, Catalog # 6002-380, UDI # 03661540600050 Product Usage: automated chemistry analyzer intended for clinical use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0153-2020·2019-10-23

    Roche Cobas c Bilirubin Total Gen.3 Recalled for Quality Control Issues

    Roche Diagnostics is recalling 2,304 units of the Cobas c Bilirubin Total Gen.3 in vitro test due to low quality control recovery and invalid calibration.

    Product
    Cobas c Bilirubin Total Gen.3 Catalog Number: 05795419190 - Product Usage: In vitro test for the quantitative determination of the total bilirubin in serum and plasma of adults and neonates on Roche/Hitachi cobas c systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0142-2020·2019-10-23

    KVK-Tech Recalls Methylphenidate Hydrochloride Oral Solution Due to Foreign Particles

    KVK-Tech is recalling 384 bottles of Methylphenidate Hydrochloride Oral Solution because of the presence of fiber particles.

    Product
    Methylphenidate Hydrochloride Oral Solution 5mg per 5mL, 500 mL Bottle, Sugar Free Alcohol Free, Rx Only, Mfd by: KVK Tech, Inc., Newtown, PA 18940, NDC 10702-0163-50.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0152-2020·2019-10-23

    Roche Diagnostics Recalls cobas Integra Albumin Gen.2 Test Kits

    Roche Diagnostics is recalling cobas Integra Albumin Gen.2 test kits due to low quality control recovery and invalid calibration.

    Product
    Roche Diagnostics cobas Integra Albumin Gen.2 Catalog Number: 05166861190 - Product Usage: In vitro test for the quantitative determination of the albumin in human serum and plasma on Roche/Hitachi cobas c systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·20010·2019-10-22

    Blackhawk T-Series L2C Gun Holsters Recalled for Injury Hazard

    Federal Cartridge is recalling Blackhawk T-Series L2C gun holsters because the design can accidentally change a firearm's safety switch, posing an injury risk.

    Product
    Blackhawk T-Series L2C gun holsters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V753000·2019-10-21

    Airstream Recalls Trailers Due to Coupler Welding Defect

    Airstream is recalling 2019-2020 travel trailers because improper welding may cause the coupler to separate from the tow ball, increasing crash risk.

    Product
    AIRSTREAM — AIRSTREAM GLOBETROTTER, FLYING CLOUD, INTERNATIONAL, SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19E073000·2019-10-21

    H&H Sports Recalls VCAN V531 Motorcycle Helmets for Retention Failure

    H&H Sports Protection is recalling VCAN V531 motorcycle helmets sold on Amazon because the retention system may fail, allowing the helmet to separate from the head during a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·102-2019·2019-10-18

    George's Prepared Foods Recalls Ready-to-Eat Pork and Turkey Sausage Patties

    George's Prepared Foods is recalling approximately 6,444 pounds of ready-to-eat pork and turkey sausage patties due to possible Salmonella contamination.

    Product
    Gold Creek Foods, LLC — George's Prepared Foods Recalls Ready-To-Eat Pork and Turkey Products due to Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·100-2019·2019-10-18

    T & R Enterprise USA Recalls Meat and Poultry Egg Rolls Due to Insanitary Conditions

    T & R Enterprise USA Inc. is recalling approximately 126,000 pounds of meat and poultry egg roll products produced under insanitary conditions. The products were shipped to institutional locations in Georgia and Missouri.

    Product
    Sinzenard International Foods — T & R Enterprise USA Inc. Recalls Meat and Poultry Products Due to Insanitary Conditions
    Category
    Food
    Distribution
    2 states
  • SevereUSDA FSIS·099-2019·2019-10-18

    MawMaw's Chicken Pies Recalls Chicken and Meat Products for Undeclared Allergens

    MawMaw's Chicken Pies is recalling chicken pie and meatloaf products in North Carolina because they contain undeclared milk and soy allergens.

    Product
    MawMaw's Chicken Pies — MawMaw's Chicken Pies Recalls Chicken and Meat Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • SevereCPSC·20704·2019-10-18

    Soft Play Recalls Spider Climb Playground Climbers Due to Fall Hazard

    Soft Play LLC is recalling Spider Climb playground climbers installed in McDonald's restaurants due to a fall hazard. The platforms are spaced too far apart, posing a risk to children.

    Product
    Spider Climb playground climbers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·101-2019·2019-10-18

    Pride of Florida Recalls Raw Beef Products for E. Coli O157:H7 Risk

    Pride of Florida is recalling approximately 64,797 pounds of raw beef products due to possible E. coli O157:H7 contamination. No illnesses have been reported.

    Product
    Pride Enterprise Food Products — Pride of Florida Recalls Beef Products due to Possible E. Coli O157:H7 Contamination
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·19V750000·2019-10-18

    Polaris Recalls 2015-2019 Slingshot Motorcycles for Electrical Fuse Defect

    Polaris is recalling 2015-2019 Slingshot motorcycles because excessive electrical current may damage battery fuse terminals, potentially causing loss of lighting or power steering and increasing crash risk.

    Product
    POLARIS — POLARIS SLINGSHOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V743000·2019-10-18

    Subaru Recalls Impreza and Crosstrek for Electrical Software Defect

    Subaru is recalling 2017-2019 Impreza and 2018-2019 Crosstrek vehicles because a software defect may cause the engine to stall while driving, increasing crash risk.

    Product
    SUBARU — SUBARU IMPREZA, CROSSTREK
    Category
    Vehicle
    Distribution
    Distributed nationwide

Looking for a different month? Back to 2019.