The Recall Desk

Archive

March 2020 recalls

515 recalls were announced in March 2020.

What the numbers show

Critical
16
Severe
165
High
214
Moderate
96
Low
24

Of the 515 recalls this month scored against our rubric, 3% are Critical, 32% are Severe.

Which agencies issued them

101–200 of 515

  • ModerateFDA (Devices)·Z-1486-2020·2020-03-25

    Philips Allura Exper FD Series X-Ray Generator Recall

    Philips is recalling Allura Exper FD Series X-ray generators because a capacitor may fail after electrical surges, preventing image acquisition.

    Product
    Allura Exper FD Series. System codes 722003 722010 722022 722005 722011 722019 722001 722002 722006 722012 722008 722013 722020 722025 722015 722023 722038 889006 889016 889009 722005 The device is an X-Ray Generator.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1050-2020·2020-03-25

    Breckenridge Recalls Solifenacin Succinate Tablets Due to Manufacturing Deviations

    Breckenridge Pharmaceutical is recalling specific lots of Solifenacin Succinate Tablets because manufacturing deviations may have resulted in the product converting to Solifenacin Tartrate.

    Product
    Solifenacin Succinate Tablets, 5mg, packaged in a) 30-count bottles (NDC 51991-893-33) and b) 90-count bottles (NDC 51991-893-90) Distributed by: Breckenridge Pharmaceutical, Inc. Boca Raton, FL 33487; Manufactured by: Piramal Enterprises Limited Plot No 67-70, Sector -2 Pithampu
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1510-2020·2020-03-25

    Arthrex Recalls Low Profile Screws Due to Incorrect Length

    Arthrex, Inc. is recalling 20 units of Low Profile Screws because they are 6 mm longer than intended. The defect may affect bone fixation.

    Product
    Low Profile Screw, 4.5 x 20 mm The Low Profile ScrewTM, 4.5 x 20 mm, AR-8545-20, is used with the Ankle Fusion Line of plates and is intended to provide internal unicortical or bicortical bone fixation.
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-1496-2020·2020-03-25

    Siemens Artis Q.zen Angiography Systems Recalled for Software Movement Issue

    Siemens is recalling Artis Q.zen angiography systems because a software issue could block stand and table movements.

    Product
    Artis Q.zen Biplane, Model No. 10848355 Artis Q.zen Ceiling, Model No. 10848354 Artis Q.zen Floor, Model No. 10848353 Product Usage: Artis is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1511-2020·2020-03-25

    Boston Scientific LATITUDE Programming System Software Update Recall

    Boston Scientific is recalling four LATITUDE Programming System devices that downloaded unapproved software applications.

    Product
    Boston Scientific, LATITUDE Programming System, Model 3300 - Product Usage:The Boston Scientific LATITUDE Programming System is intended for use in hospital and clinical environments to communicate with Boston Scientific implantable systems. The software in use controls all commu
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1042-2020·2020-03-25

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Therapeutics is recalling Daytrana (methylphenidate) patches because the delivery system failed mechanical peel and shear specifications.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1058-2020·2020-03-25

    Jubilant Cadista Recalls Pantoprazole Sodium Tablets Due to CGMP Deviations

    Jubilant Cadista Pharmaceuticals is recalling 89,376 bottles of Pantoprazole Sodium Delayed-Release Tablets due to dark brown discoloration on tablet edges.

    Product
    Pantoprazole Sodium Delayed-Release Tablets, USP, 40 mg, 90 count bottle, Rx Only, Manufactured by Jubilant Generics Ltd, Roorkee-247661 India, NDC 59746-284-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1044-2020·2020-03-25

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Therapeutics is recalling Daytrana (methylphenidate) patches because the delivery system failed mechanical peel and shear specifications.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1043-2020·2020-03-25

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Therapeutics is recalling Daytrana (methylphenidate) transdermal patches because the delivery system failed mechanical peel and shear specifications.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1029-2020·2020-03-25

    Strides Pharma Recalls Potassium Chloride Tablets Due to Oversized Size

    Strides Pharma Science Limited is recalling specific lots of Potassium Chloride Extended-Release Tablets because oversized tablets were found.

    Product
    POTASSIUM CHLORIDE — POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V175000·2020-03-23

    2021 Ford E-350 and E-450 wire harness may damage fuel pump and ABS

    Ford is recalling 2021 E-350 and E-450 vehicles because a rear wire harness may contact the frame and damage circuits for the fuel pump and anti-lock braking system, potentially causing engine stall or loss of braking control.

    Product
    FORD — FORD E-450, E-350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V176000·2020-03-23

    Freightliner Trucks Recalled for Axle Lubrication Defect

    Daimler Trucks is recalling 2019-2020 Freightliner M2 and 108SD trucks because insufficient axle lubrication may damage wheel bearings, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2, 108SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V177000·2020-03-23

    Ford Recalls 2014-2016 Vehicles for Door Latch Defect

    Ford is recalling 2014-2016 Fiesta, Fusion, and Lincoln MKZ vehicles because a door latch component may break, causing doors to open while driving.

    Product
    LINCOLN — LINCOLN, FORD MKZ, FUSION, FIESTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V168000·2020-03-20

    Terex Recalls 2009-2016 Aerial Devices Due to Lift Cylinder Defect

    Terex is recalling 2009-2016 TCX and SML aerial devices because lift cylinder rod eyes may fail, causing the boom to drift down and increasing injury risk.

    Product
    TEREX — TEREX TCX, SML
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V171000·2020-03-20

    Newmar Recalls Motorhomes Due to Insufficiently Tightened Brake Caliper Bolts

    Newmar is recalling specific 2019-2020 motorhomes because brake caliper mounting bolts may be loose, which can reduce braking effectiveness and increase crash risk.

    Product
    NEWMAR — NEWMAR LONDON AIRE, ESSEX, VENTANA, VENTANA LE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E014000·2020-03-20

    Carrier Truck Refrigeration Units Recalled for Fire Risk

    Carrier is recalling certain Transicold Supra series truck refrigeration units because improperly routed cables may chafe and cause a fire.

    Product
    EQUIPMENT:ELECTRICAL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E015000·2020-03-20

    Carrier Trailer Refrigeration Units Recalled for Fire Risk

    Carrier is recalling 107 trailer refrigeration units because a generator harness may chafe, causing electrical arcing and increasing the risk of a fire.

    Product
    EQUIPMENT:ELECTRICAL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V173000·2020-03-20

    Mercedes-Benz Recalls S560 Vehicles Due to Engine Oil Plug Defect

    Mercedes-Benz is recalling 2018-2019 S560 and Maybach S560 vehicles because engine oil plugs may fail under high load, causing oil leaks or engine stalls that increase crash risk.

    Product
    MERCEDES-MAYBACH — MERCEDES-MAYBACH, MERCEDES-BENZ S 560 4MATIC, S560
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E016000·2020-03-20

    Harbor Freight Recalls Pittsburgh Automotive 6 Ton Heavy Duty Steel Jack Stands

    Harbor Freight is recalling 454,000 Pittsburgh Automotive 6 Ton Heavy Duty Steel Jack Stands because the ratchet teeth may not engage properly, risking sudden failure and injury.

    Product
    EQUIPMENT:MECHANICAL:INTEGRATED JACK/LEVELER/STABILIZER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V158000·2020-03-19

    Forest River Recalls Vans Due to Transmission Shifter Cable Separation

    Forest River is recalling 2016-2020 vans because the transmission shifter cable may disconnect, causing unintended vehicle movement and crash risk.

    Product
    LONE STAR HANDICAP VANS — LONE STAR HANDICAP VANS, FOREST RIVER, COACHMEN L1 VAN, REV, ORION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V159000·2020-03-19

    Tremcar Recalls 2018-2020 Semi-Trailers Due to Brake Washer Fracture Risk

    Tremcar is recalling 2018-2020 406 and 407 semi-trailers because brake actuator washers may fracture, potentially reducing braking ability and increasing crash risk.

    Product
    TREMCAR — TREMCAR 406 SEMI-TRAILER, 407 SEMI-TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V164000·2020-03-19

    BMW Recalls 2020 Models for Front Seat Belt Sensor Defect

    BMW is recalling 2020 models because front seat belt sensors may misread occupants, causing improper airbag and pretensioner deployment.

    Product
    BMW — BMW M850I, M340I, X3, X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V161000·2020-03-19

    Forest River Recalls 2019-2020 Motorhomes Due to Brake Caliper Bolt Issue

    Forest River is recalling 2019-2020 Berkshire and Sportscoach motorhomes because brake caliper mounting bolts may be insufficiently tightened, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN BERKSHIRE, SPORTSCOACH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V170000·2020-03-19

    Husqvarna 701 Motorcycles Recalled for Fuel Leak Fire Risk

    KTM is recalling 2018-2020 Husqvarna Vitpilen and Svartpilen 701 motorcycles because fuel may leak from the pump area, increasing fire risk.

    Product
    HUSQVARNA — HUSQVARNA VITPILEN 701, SVARTPILEN 701
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V165000·2020-03-19

    BMW Recalls 2020 R 1250 RT and GS Motorcycles for Driveline Defect

    BMW is recalling 2020 R 1250 RT and GS motorcycles because a damaged pivot pin may loosen the final drive connection, increasing crash risk.

    Product
    BMW — BMW R 1250 RT, R 1250 GS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E013000·2020-03-19

    BMW Recalls Motorcycle Brake Fluid Reservoir Caps for Labeling Defect

    BMW is recalling specific motorcycle brake fluid reservoir caps because they may not clearly state the required brake fluid type, potentially leading to improper maintenance.

    Product
    BMW — BMW R NINE T SCRAMBLER, R 1250 R, R 1250 RS, R NINE T
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20096·2020-03-19

    Thule Recalls Sleek Car Seat Adapters Due to Fall Hazard

    Thule is recalling Sleek Car Seat Adapters because plastic brackets can break, posing a fall hazard to infants. No injuries have been reported.

    Product
    Thule Sleek Car Seat Adapters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V166000·2020-03-19

    BMW Recalls Motorcycles Due to Unclear Brake Fluid Reservoir Cap Labeling

    BMW is recalling specific 2018-2020 motorcycles because the brake fluid reservoir cap may not clearly state the required fluid type, potentially leading to improper maintenance.

    Product
    BMW — BMW R NINE T SCRAMBLER, R NINE T RACER, R NINE T, R 1250 RS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20099·2020-03-19

    Crate and Barrel Recalls Miles Glass Pitchers Due to Laceration Hazard

    Crate and Barrel is recalling Miles Glass Pitchers with Wood Lid because the handle can break, posing a laceration hazard. No injuries have been reported.

    Product
    Miles Glass Pitchers with Wood Lid
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20723·2020-03-19

    Plant Therapy Recalls Wintergreen Oils for Non-Child-Resistant Packaging

    Plant Therapy is recalling specific wintergreen essential oils and blends because the packaging is not child-resistant, posing a risk of poisoning to young children.

    Product
    Plant Therapy Wintergreen, Organic Wintergreen, Muscle Aid Synergy Blend, Tingly Mint Synergy Blend, and Vein Aid Synergy Blend Oils
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20726·2020-03-19

    Kawasaki Recalls MULE PRO Utility Vehicles Due to Steering Shaft Wear

    Kawasaki is recalling approximately 80,000 MULE PRO off-highway utility vehicles because excessive steering shaft wear can affect steering control, posing a crash hazard.

    Product
    Kawasaki MULE PRO off-highway utility vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0829-2020·2020-03-18

    Shearer's Yellow Tortilla Chips Recalled for Undeclared Milk

    Shearer's Snacks is recalling specific lots of Yellow tortilla chips due to undeclared milk. The product was shipped to two distributors and is fully accounted for.

    Product
    Shearer's Yellow tortilla chips, round Mini and Restaurant sizes, packaged in clear film pillow bags in the following weights: 1oz (100 count per case), 1.5oz (72 count per case), 2oz (60 count per case), and a bulk case16oz bags (10 count per case)
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-1442-2020·2020-03-18

    CME BodyGuard Microset Infusion Sets Recalled for Fluid Under-Delivery

    CME America is recalling BodyGuard Microset infusion sets because they may under-deliver fluids when used with specific infusion pump systems.

    Product
    BodyGuard Microset REF A120-003XYVA, Sterile EO, Tubing: 150 in. (380 cm), Prime Vol: approx. 8ml Product Usage: The BodyGuard Infusion Pump System is designed to transfer medication and fluids intravenously.
    Category
    Medical Device
    Distribution
    4 states
  • SevereFDA (Food)·F-0832-2020·2020-03-18

    Chocolate Dairy Powder Recalled Due to Potential Metal Fragment Contamination

    International Food Products Corporation is recalling 21 bags of chocolate dairy powder because an ingredient may have been contaminated with metal fragments.

    Product
    Profile Food Ingredients, 10# Choc Dairy Pwd PFI-1010, packaged in 50 lb bags.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0827-2020·2020-03-18

    Domino Foods Recalls Great Value Sugar Due to Metal Contamination

    Domino Foods Inc. is recalling Great Value Pure Granulated Sugar because it may contain metal pieces. The product was shipped to one consignee in Pennsylvania.

    Product
    GREAT VALUE¿ Pure Granulated Sugar, 10 lbs. Sold as individual bags on a unitized 1/2 pallet 78 bags to a 1/2 pallet.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0812-2020·2020-03-18

    Tova Industries Recalls Shaver Foods Gravy Beef Due to Metal Shavings

    Tova Industries is recalling Shaver Foods brand Gravy Beef because of possible metal shavings in the ingredient. The product was distributed to 11 states and the United Arab Emirates.

    Product
    Shaver Foods brand Gravy Beef, Item #35089, in 2 lb. metallic pouches, 12 pouches per case.
    Category
    Food
    Distribution
    11 states
  • SevereNHTSA·20V154000·2020-03-18

    Bentley Recalls Bentayga Vehicles Due to Third-Row Seat Belt Defect

    Bentley is recalling 2018-2020 Bentayga vehicles with third-row seats because the upper seat belt attachment may detach in a crash, increasing injury risk.

    Product
    BENTLEY — BENTLEY BENTAYGA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1009-2020·2020-03-18

    Redline Pharmacy Recalls Ertapenem Injectable Due to Processing Control Issues

    Redline Pharmacy Solutions is recalling 8 doses of Ertapenem Injectable due to a lack of processing controls. The product was sold to patients in Nebraska.

    Product
    Ertapenem in 100ML 0.9% NACL 1GM Injectable, Redline Specialty Pharmacy, 2415 Osborne Drive E, #100 Hastings, NE 68901
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1011-2020·2020-03-18

    Redline Pharmacy Recalls Morphine Sulfate Due to Processing Controls

    Redline Pharmacy Solutions is recalling Morphine Sulfate (MITIGO) 5 mg/mL intrathecal syringes due to a lack of processing controls.

    Product
    Morphine Sulfate (MITIGO), 5 mg/mL intrathecal, 40 mL per syringe. Redline Specialty Pharmacy, 2415 Osborne Drive E, #100 Hastings, NE 68901
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1427-2020·2020-03-18

    HeartWare HVAD System Battery Charger Recalled for Adapter Insertion Risk

    Heartware, Inc. is recalling 5,489 HeartWare HVAD System Battery Chargers because users may mistakenly insert the AC adapter into the HVAD Controller power port.

    Product
    HeartWare HVAD System Battery Charger The HeartWare HVAD System is indicated for hemodynamic support in patients with advanced, refractory left ventricular heart failure; either as a Bridge to Cardiac Transplantation (BTT), myocardial recovery, or as Destination Therapy (DT)
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Drugs)·D-1010-2020·2020-03-18

    Redline Pharmacy Recalls Vancomycin Injectable Due to Processing Control Deficiencies

    Redline Pharmacy Solutions is recalling 3 doses of Vancomycin 900MG Injectable due to a lack of processing controls. The product was sold to patients in Nebraska.

    Product
    Vancomycin 900MG in 100ML 0.9% NACL Injectable, Redline Specialty Pharmacy, 2415 Osborne Drive E, #100 Hastings, NE 68901
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1476-2020·2020-03-18

    Qiagen Rotor-Gene Q Software Recall for Incorrect Concentration Reporting

    Qiagen is recalling Rotor-Gene Q instruments with software version 2.3.4 because a bug causes concentration results to be reported as logarithmic values, potentially leading to false negative test results.

    Product
    QIAGEN Rotor Gene Q Software version 2.3.4. Real-time PCR analyzer designed for rapid thermalcycling and real-time detection of PCR assays.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1003-2020·2020-03-18

    American Health Packaging Recalls Ranitidine Tablets Due to NDMA Levels

    American Health Packaging is recalling 53,619 cartons of Ranitidine Tablets, 150 mg, due to potential N-Nitrosodimethylamine (NDMA) amounts above FDA-established levels.

    Product
    Ranitidine Tablets, USP, 150 mg, 100 Tablets (10 tablets x 10 blister card), Rx Only, Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC carton: 60687-322-01; NDC Unit Dose Card: 60687-322-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1007-2020·2020-03-18

    Redline Pharmacy Recalls Morphine Sulfate Due to Processing Control Deficiencies

    Redline Pharmacy Solutions is recalling Morphine Sulfate 20 mg/mL intrathecal syringes due to a lack of processing controls. The product was sold to patients in Nebraska.

    Product
    Morphine Sulfate, 20 mg/mL intrathecal, 20 mL per syringe. Redline Specialty Pharmacy, 2415 Osborne Drive E, #100 Hastings, NE 68901
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1004-2020·2020-03-18

    Precision Dose Recalls Ranitidine Oral Solution Due to NDMA Impurity

    Precision Dose Inc. is recalling Ranitidine Oral Solution because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).

    Product
    Ranitidine Oral Solution, USP, 150 mg/10 mL, [10 mL x 30 Unit Dose Cups per case, NDC: 68094-204-62; 10 mL x 100 Unit Dose Cups per case, NDC: 68094-204-61; Unit Dose Cup NDC: 68094-204-59], Rx only, Precision Dose, Inc., South Beloit, IL 61080
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0831-2020·2020-03-18

    Maryland Packaging Recalls Pure Cane Sugar Due to Metal Wire

    Maryland Packaging, LTD. is recalling 4,056 bags of Pure Cane Granulated Sugar in Pennsylvania and Maryland because the product may contain a metal wire.

    Product
    Pure Cane Granulated Sugar, Single 10 lb. package, 156 paper bags on 2 1/2 CHEP pallets
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0817-2020·2020-03-18

    Tova Industries Recalls American Bounty Chili Mix Due to Metal Shavings

    Tova Industries is recalling American Bounty Chili Mix w/Beans because of possible metal shavings in an ingredient. The recall covers 225 cases distributed to 11 states and the UAE.

    Product
    American Bounty brand Chili Mix w/Beans, Item #46628, in 20.8 oz. metallic pouches, 6 pouches per case.
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-0801-2020·2020-03-18

    Tova Industries Recalls American Bounty Vanilla Icing Mix Due to Metal Shavings

    Tova Industries is recalling American Bounty brand Icing Mix Vanilla due to possible metal shavings in the ingredient. The recall covers 104 cases distributed to 11 states and the United Arab Emirates.

    Product
    American Bounty brand Icing Mix Vanilla, Item #32595, in 5 lb. metallic pouches, 6 pouches per case.
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-0814-2020·2020-03-18

    Tova Industries Recalls Shaver Foods Gravy Chicken Due to Metal Shavings

    Tova Industries is recalling Shaver Foods brand Gravy Chicken because it may contain metal shavings. The product was distributed to 11 states and the United Arab Emirates.

    Product
    Shaver Foods brand Gravy Chicken, Item #35213, in 2 lb. metallic pouches, 12 pouches per case.
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-0819-2020·2020-03-18

    Tova Industries Recalls MJ Kellner Vegan Milk Replacer Due to Metal Shavings

    Tova Industries is recalling MJ Kellner brand Vegan Soy Based Milk Replacer because of possible metal shavings in the ingredient.

    Product
    MJ Kellner brand Milk Replacer, Vegan, Soy Based, Item #80286, in 22.7g, metallic pouch, 300 pouches per case
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-0824-2020·2020-03-18

    Meijer Recalls Chicken Cobb Salad Due to Undeclared Wheat Allergen

    Meijer is recalling Chicken Cobb Salad containers that may contain undeclared wheat croutons. Consumers with wheat allergies should not eat the product.

    Product
    Meijer Chicken Cobb Salad 10.75oz. in Clear plastic, sectioned, container; UPC 71928367932
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0816-2020·2020-03-18

    Tova Industries Recalls William R Hill Beef Soup Base Due to Metal Shavings

    Tova Industries is recalling William R Hill brand Soup Base Beef No MSG due to possible metal shavings in the ingredient.

    Product
    William R Hill brand Soup Base Beef No MSG, Item #41175, in 1 lb. metallic pouches, 12 pouches per case.
    Category
    Food
    Distribution
    11 states
  • HighCPSC·20725·2020-03-18

    Earth Sonnets Recalls Wintergreen Essential Oil for Packaging Defect

    Earth Sonnets is recalling Wintergreen Essential Oil because the packaging is not child-resistant, posing a risk of poisoning to young children.

    Product
    Earthsonnets Wintergreen (Gualtheria procumbens) Essential Oil
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V151000·2020-03-18

    Lamborghini Recalls 2020 Aventador SVJ Models for Door Handle Defect

    Lamborghini is recalling 26 2020 Aventador SVJ vehicles because the interior door handle mechanism may fail, preventing the door from opening from inside.

    Product
    LAMBORGHINI — LAMBORGHINI AVENTADOR SVJ COUPE, AVENTADOR SVJ ROADSTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0802-2020·2020-03-18

    Tova Industries Recalls Shaver Foods Frosting Mix Due to Metal Shavings

    Tova Industries is recalling Shaver Foods brand Frosting Mix Chocolate Texas due to possible metal shavings in the ingredient.

    Product
    Shaver Foods brand Frosting Mix Chocolate Texas, Item #32637, in 5 lb. metal pouch, 6 pouches per case.
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-0815-2020·2020-03-18

    Tova Industries Recalls Shaver Foods Vanilla Frosting Mix Due to Metal Shavings

    Tova Industries is recalling Shaver Foods brand Frosting Mix Vanilla due to possible metal shavings in the ingredient. The product was distributed to 11 states and the United Arab Emirates.

    Product
    Shaver Foods brand Frosting Mix Vanilla, Item #32600, in 5 lb. metallic pouches, 6 pouches per case.
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-0810-2020·2020-03-18

    Riverside Brown Gravy Recalled for Possible Metal Shavings

    Tova Industries is recalling Riverside brand Brown Gravy due to possible metal shavings in an ingredient. The recall affects 42 cases distributed to 11 states and the UAE.

    Product
    Riverside brand Brown Gravy, Item #35186, in 14 oz. metallic pouches, 48 pouches per case.
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-1467-2020·2020-03-18

    RayStation 9A Software Recall for Pitch and Roll Correction Errors

    RaySearch Laboratories is recalling one RayStation/RayPlan 9A system in Tennessee due to potential errors in position propagation when pitch or roll corrections are applied.

    Product
    RayStation/RayPlan 9A, Build Number 9.0.0.113, stand-alone software treatment planning system
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Food)·F-0823-2020·2020-03-18

    Lindt Dark Chocolate Bars Recalled for Undeclared Milk Allergen

    Lindt & Sprungli is recalling specific Lindt Excellence 85% Cocoa Dark Chocolate Bars in New York because they may contain undeclared milk allergens.

    Product
    Lindt Excellence 85% Cocoa Dark Chocolate Bars, 3.5 oz.(100g)
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1465-2020·2020-03-18

    RayStation 8B Software Recalled for Pitch and Roll Correction Errors

    RaySearch Laboratories is recalling one RayStation 8B treatment planning system in Tennessee due to a software error that may cause incorrect position values.

    Product
    RayStation/RayPlan 8B Service Pack 1, Build Number 8.1.1.8, stand-alone software treatment planning system
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1472-2020·2020-03-18

    Medicrea Recalls Pedicle Screws Due to Incorrect Component Orientation

    Medicrea International is recalling 3,529 pedicle screws because an internal component was assembled incorrectly, which may cause the tulip head to disengage from the screw shank.

    Product
    Pedicle Screws, multiple sizes, Article Nos. B36004525 B36004530 B36004535 B36004540 B36004545 B36004550 B36004555 B36005530 B36005535 B36005540 B36005545 B36005550 B36005555 B36005560 B36006530 B36006535 B36006540 B36006545 B36006550 B36006555 B36006560 B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V152000·2020-03-18

    BMW Recalls X3 and X4 Models for Instrument Panel Casing Defect

    BMW is recalling 2018-2020 X3 and 2019-2020 X4 vehicles because the instrument panel casing may not be tightened properly, posing an injury risk during air bag deployment.

    Product
    BMW — BMW X3, X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20093·2020-03-18

    Belle Chemical Recalls Sodium and Potassium Hydroxide for Packaging Defects

    Belle Chemical is recalling sodium and potassium hydroxide products because they lack required child-resistant packaging and proper hazard labeling.

    Product
    Sodium Hydroxide, Lye/Caustic Soda and Potassium Hydroxide, Caustic Potash Ash
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1458-2020·2020-03-18

    Nextremity Solutions Recalls Nextra Hammertoe Correction System Due to Driver Defect

    Nextremity Solutions is recalling 190 units of the Nextra Hammertoe Correction System because the driver may be oversized, making it difficult to remove from the implant.

    Product
    Nextra Hammertoe Correction System-4.5MM Middle, 3.2MM Proximal, SS, Sterile. REF: NX-4532K - Product Usage: The Nextra Hammertoe Correction System is a system of implants and associated instruments which is indicated for small bone reconstruction limited to inter-digital repair
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1473-2020·2020-03-18

    Medicrea Iliac Screws Recalled Due to Incorrect Component Orientation

    Medicrea International is recalling 3,529 Iliac Screws because an internal component was assembled incorrectly, which may cause the tulip head to disengage from the shank.

    Product
    Iliac Screws, multiple sizes, Article Nos. B36020500 B36020570 B36020580 B36020590 B36027500 B36027570 B36027580 B36027590 B36028500 B36028570 B36028580 B36028590 B36029500 B36029570 B36029580 B36029590 Screws manufactured in titanium alloy Ti-6Al-4V LI confor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0818-2020·2020-03-18

    Tova Industries Recalls Indianhead Vanilla Crystals Due to Metal Shavings

    Tova Industries is recalling Indianhead Vanilla Crystals because of possible metal shavings in the ingredient. The product was distributed to 11 states and the United Arab Emirates.

    Product
    Indianhead brand Vanilla Crystals, Item #80580, in 10 lb. bag inside box
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-0811-2020·2020-03-18

    Shaver Foods Gravy Brown Roast Recalled for Possible Metal Shavings

    Tova Industries is recalling Shaver Foods Gravy Brown Roast due to possible metal shavings in an ingredient. The product was distributed to 11 states and the United Arab Emirates.

    Product
    Shaver Foods brand Gravy Brown Roast, Item #35586, in 13 oz. metallic pouches, 6 pouches per case.
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-1468-2020·2020-03-18

    RayStation 9B Software Recalled for Pitch and Roll Correction Errors

    RaySearch Laboratories AB is recalling one RayStation/RayPlan 9B software system in Tennessee due to potential errors in position calculations during pitch or roll corrections.

    Product
    RayStation/RayPlan 9B, Build Number 9.1.0.933, stand-alone software treatment planning system
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Food)·F-0807-2020·2020-03-18

    Indianhead Beef Soup Base Recalled for Possible Metal Shavings

    Tova Industries is recalling Indianhead brand Soup Base Beef Premium due to possible metal shavings in the ingredient.

    Product
    Indianhead brand Soup Base Beef Premium, Item #41165, in 35 lb. pails.
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-1475-2020·2020-03-18

    Getinge 88-Series Washer Disinfectors Recalled for Chamber Leakage Risk

    Maquet Cardiovascular is recalling Getinge 88-Series washer disinfectors because ruptured spot welds may cause water leakage, posing slip and infection risks.

    Product
    Getinge 88-Series-washer disinfectors intended for cleaning, disinfection and drying Model Number: 88-5 Part Number: 88-103; 88-203
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1464-2020·2020-03-18

    RayStation 8B Software Recalled for Pitch and Roll Correction Errors

    RaySearch Laboratories AB is recalling one RayStation 8B software system in Tennessee due to potential errors in tabletop position propagation.

    Product
    RayStation/RayPlan 8B, Build Number 8.1.0.47, stand-alone software treatment planning system
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Food)·F-0805-2020·2020-03-18

    Good Source Chicken Flavored Rice Meal Recalled for Possible Metal Shavings

    Tova Industries is recalling Good Source Chicken Flavored Rice Meal due to possible metal shavings in the ingredient. The recall covers 6 cases distributed to 11 states and the UAE.

    Product
    Good Source brand Chicken Flavored Rice Meal, Item #47790, in 2 lb. metal pouches, 14 pouches per case.
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-0820-2020·2020-03-18

    Tova Industries Recalls American Bounty Beef Soup Base Due to Metal Shavings

    Tova Industries is recalling American Bounty brand Soup Base Beef No MSG due to possible metal shavings in the ingredient. The product was distributed to 11 states and the United Arab Emirates.

    Product
    American Bounty brand Soup Base Beef No MSG, Item #41178, 1 lb, metallic pouch, 12 pouches per case
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-0821-2020·2020-03-18

    Tova Industries Recalls Chicken Soup Base Due to Possible Metal Shavings

    Tova Industries is recalling William R Hill brand Soup Base Chicken due to possible metal shavings in the ingredient. The recall affects 140 cases distributed to 11 states and the United Arab Emirates.

    Product
    William R Hill brand Soup Base Chicken, Item #41178, 1 lb, metallic pouch, 6 pouches per case
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-1466-2020·2020-03-18

    RayStation 8B Software Recalled for Pitch and Roll Correction Errors

    RaySearch Laboratories is recalling one RayStation 8B software system in Tennessee due to a defect that causes incorrect position values when pitch or roll corrections are applied.

    Product
    RayStation/RayPlan 8B Service Pack 2, Build Number 8.1.2.5, stand-alone software treatment planning system
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1450-2020·2020-03-18

    Medtronic Simulus 850 Sizer Kits Recalled Due to Porcine Tissue Contact

    Medtronic is recalling six Simulus 850 Semi Rigid Ring/Band Accessory Kits because demonstration units may have contacted porcine tissue.

    Product
    Medtronic Simulus 850 Semi Rigid Ring/Band Accessory Kit Used to size a patient's mitral or tricuspid valve in cardiac procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1005-2020·2020-03-18

    Acetaminophen Tablets Recalled Due to Foreign Tablet Contamination

    H J Harkins Company Inc is recalling Acetaminophen 500 mg tablets because a foreign Women's Prenatal tablet was found in the product.

    Product
    Acetaminophen 500 mg tablet packaged in a) 30-count bottles ( NDC 52959-0002-30), b) 42-count bottles (NDC 52959-0002-42), c) 45-count bottles (NDC 52959-0002-45) and e) 50-count bottles (NDC 52959-0002-50) Repack: H.J. Harkins Co., Inc. Grover Beach, CA 93433
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1463-2020·2020-03-18

    RayStation Software Recall for Potential Treatment Planning Errors

    RaySearch Laboratories is recalling one RayStation 8A system in Tennessee due to a software defect that may cause incorrect treatment planning calculations.

    Product
    RayStation/RayPlan 8A Service Pack 1, Build Number 8.0.1.10, stand-alone software treatment planning system
    Category
    Medical Device
    Distribution
    1 state
  • HighNHTSA·20V155000·2020-03-18

    Daimler Vans Recalls 2018-2019 Sprinter Vehicles for Incorrect Spare Tire Label

    Daimler Vans is recalling 2018-2019 Mercedes-Benz and Freightliner Sprinter vehicles because the spare tire label may list the maximum speed in kilometers per hour instead of miles per hour.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 1500, SPRINTER 2500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1452-2020·2020-03-18

    ARJOHUNTLEIGH Recalls Concerto and Basic Shower Trolleys Due to Safety Catch Failure

    ARJOHUNTLEIGH is recalling 669 Concerto and Basic Shower Trolleys because a mechanical failure in the safety catch could cause the side support to open, posing a risk of patient falls and injuries.

    Product
    Concerto & Basic Shower Trolly, Model Numbers BAB1000-01 (UDI: (01)05055982788083), BAB1000CON6102 [(01)05056097364483], BAB1007-01 [(01)05055982796255], BAB1101-01 [(01)05055982787949], BAB1102-01 [(01)05055982796156], BAB1103-01 [UDI: (01)05055982796163], BAB1107-01 [(01)05055
    Category
    Medical Device
    Distribution
    15 states

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