The Recall Desk

Archive

March 2019 recalls

999 recalls were announced in March 2019.

What the numbers show

Critical
265
Severe
394
High
255
Moderate
69
Low
16

Of the 999 recalls this month scored against our rubric, 27% are Critical, 39% are Severe.

Which agencies issued them

701–800 of 999

  • SevereFDA (Drugs)·D-0987-2019·2019-03-13

    Sunstone Organics Recalls White Vein Kratom Powder Due to Salmonella

    Sunstone Organics is recalling White Vein Kratom powder in 25, 50, and 100-gram packages because samples tested positive for Salmonella.

    Product
    White Vein Kratom, packaged in a) 25 gram powder (UPC 00859667007316), b) 50 gram powder (UPC 00859667007323), c) 100 gram powder (UPC 00859667007330), Sunstone Organics Springfield, Oregon 97473, 541-972-3327.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1141-2019·2019-03-13

    Southwind Foods Recalls Wild Dungeness Crab Cake Due to Temperature Abuse

    Southwind Foods is recalling 13 cases of Wild Dungeness Crab Cake sold at Whole Foods in California, Arizona, and Hawaii due to potential temperature abuse.

    Product
    Wild Dungeness Crab Cake; Net Weight: 12 lb - 48 x 4.0 oz. Keep Frozen Manufactured for Whole Foods Market
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0988-2019·2019-03-13

    Sunstone Organics Recalls White Vein Kratom Capsules Due to Salmonella

    Sunstone Organics is recalling White Vein Kratom capsules in 20, 60, and 150-count bottles because samples tested positive for Salmonella.

    Product
    White Vein Kratom, packaged in a) 20 count capsules (UPC 00859667007347), b) 60 count capsules (UPC 00859667007354), c) 150 count capsules (UPC 00859667007361), Sunstone Organics Springfield, Oregon 97473 541-972-3327.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1171-2019·2019-03-13

    Kingston Pharma Recalls DG Baby Gripe Water Due to Undissolved Ingredient

    Kingston Pharma LLC is recalling DG Baby Gripe Water herbal supplements because they contain an undissolved ingredient, citrus flavonoid.

    Product
    DG Baby Gripe Water herbal supplement with organic ginger and fennel extracts, 4 FL OZ (120 mL) Liquid Dietary Supplement UPC: 8 54954 00246 3
    Category
    Food
    Distribution
    43 states
  • SevereFDA (Food)·F-1148-2019·2019-03-13

    Stacy's Pita Chips Recalled for Potential Undeclared Milk

    Frito-Lay is recalling Stacy's Simply Naked Pita Chips due to a potential undeclared milk allergen. Consumers should check their bags for specific dates and codes.

    Product
    Stacy's Simply Naked Pita Chips 7 1/3 ounce bags
    Category
    Food
    Distribution
    0 states
  • SevereNHTSA·19V197000·2019-03-13

    Newmar Recalls 2017-2019 Ventana Motorhomes for Loose Steering Bolts

    Newmar is recalling 2017-2019 Ventana motorhomes because loose steering and tie rod arm bolts may separate, causing loss of vehicle control and increasing crash risk.

    Product
    NEWMAR — NEWMAR VENTANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0988-2019·2019-03-13

    Maquet XS Flat Screen Monitor Holder Recalled for Grounding Defect

    Getinge is recalling six Maquet XS Flat Screen Monitor Holders in Arizona and Texas because they may not meet grounding requirements, posing a risk of electric shock.

    Product
    Maquet XS Flat Screen Monitor Holder, PWD50+DF XS32 K3 SPE, Configuration Part Number ARD268400140A Product Usage: This product is designed to support one or two medical grade flat screen(s) alone or in association with surgical lights.
    Category
    Medical Device
    Distribution
    2 states
  • SevereUSDA FSIS·029-2019·2019-03-13

    Monogram Meat Snacks Recalls Pork Sausage Due to Product Tampering

    Monogram Meat Snacks is recalling approximately 191,928 pounds of ready-to-eat pork sausage products due to possible product contamination from tampering. No illnesses have been reported.

    Product
    Monogram Meat Snacks, LLC — Monogram Meat Snacks, LLC Recalls Pork Sausage Products Due to Possible Product Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1154-2019·2019-03-13

    Ocean Beauty Seafoods Recalls Hot Smoked Salmon for Botulism Risk

    Ocean Beauty Seafoods is recalling Hot Smoked Salmon Variety Packs sold at Aldi due to potential Clostridium botulinum contamination from low salt content.

    Product
    Hot Smoked Salmon Variety Pack. ITEM # F3120SS9, Aldi ID# 51326. Each master case contains 12/4 oz. packs (4 packs of each flavor - Traditional, Cracked Black Pepper, and Cajun Flavored). Traditional, Hot Smoked Salmon, 4 oz. UPC 041498234881. Cajun Flavored, Hot Smoked S
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0520-2019·2019-03-13

    Vi-Jon Hydrogen Peroxide Recalled for IPA Contamination

    Vi-Jon, Inc. is recalling 32-ounce bottles of Hydrogen Peroxide First Aid Antiseptic due to the presence of Isopropyl Alcohol (IPA). The product was distributed in Ohio.

    Product
    Topical Solution USP Hydrogen Peroxide First Aid Antiseptic Oral Debriding Agent 32 Fl. Oz. (1 QT) 946 mL bottle, Distributed By: Discount Drug Mart 211 Commerce Drive, Medina, Ohio 44256 NDC 53943-871-45 UPC 0-93351-12758-8
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0518-2019·2019-03-13

    Leiter's Recalls Cefuroxime Intravitreal Injection Due to Incorrect Formulation

    Leiter's Enterprises is recalling 569 vials of Cefuroxime 10 mg/mL intravitreal injection because the drug was compounded with sterile water instead of sterile 0.9% Sodium Chloride.

    Product
    Cefuroxime 10 mg/mL in Sodium Chloride, Intravitreal injection, 1 mL in a 2mL Vial, Ophthalmic Use Only, Office Use Only, Leiter's (800) 292-6772- 17 Great Oaks Blvd., San Jose, CA 95119. NDC: 70360-007-35.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Devices)·Z-0990-2019·2019-03-13

    Maquet XS Flat Screen Monitor Holder Recalled for Grounding Defect

    Getinge is recalling four Maquet XS Flat Screen Monitor Holders in Arizona and Texas because they may not meet grounding requirements, posing a risk of electric shock.

    Product
    Maquet XS Flat Screen Monitor Holder, SAT XS32 12 SPE, Configuration Part Number ARD2SAT00130A Product Usage: This product is designed to support one or two medical grade flat screen(s) alone or in association with surgical lights.
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Devices)·Z-0987-2019·2019-03-13

    Maquet XS Flat Screen Monitor Holder Recalled for Grounding Defect

    Getinge is recalling six Maquet XS Flat Screen Monitor Holders because they may not meet grounding requirements, posing a risk of electric shock.

    Product
    Maquet XS Flat Screen Monitor Holder, XS32 SPE, Configuration Part Number ARD22201040A Product Usage: This product is designed to support one or two medical grade flat screen(s) alone or in association with surgical lights.
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0986-2019·2019-03-13

    Sunstone Organics Recalls Maeng Da Kratom Powder Due to Salmonella Contamination

    Sunstone Organics is recalling Maeng Da Kratom powder in 25, 50, and 100-gram packages due to positive Salmonella test results.

    Product
    Maeng Da Kratom, packaged in a) 25 gram powder (UPC 00859667007118), b) 50 gram powder (UPC 00859667007125), c) 100 gram powder (UPC 00859667007132), Sunstone Organics Springfield, Oregon 97473, 541-972-3327.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-0989-2019·2019-03-13

    Maquet Flat Screen Monitor Holder Recalled for Grounding Non-Compliance

    Getinge US Sales LLC is recalling six Maquet XS Flat Screen Monitor Holders because they may not meet grounding requirements, posing a risk of electric shock.

    Product
    Maquet XS Flat Screen Monitor Holder, PWD70+DF HD R XS32 K3 SPE, Configuration Part Number ARD268400150A Product Usage: This product is designed to support one or two medical grade flat screen(s) alone or in association with surgical lights.
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0989-2019·2019-03-13

    Sunstone Organics Recalls Maeng Da Kratom Capsules Due to Salmonella Contamination

    Sunstone Organics is recalling Maeng Da Kratom capsules in 20, 60, and 150-count bottles because samples tested positive for Salmonella.

    Product
    Maeng Da Kratom, packaged in a) 20 count capsules (UPC 00859667007149), b) 60 count capsules (UPC 00859667007156), c) 150 count capsules (UPC 00859667007163) , Sunstone Organics Springfield, Oregon 97473, 541-972-3327.
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Devices)·Z-0984-2019·2019-03-13

    Siemens Uroskop Omnia Fluoroscopic X-ray System Recalled for Monitor Arm Defect

    Siemens is recalling six Uroskop Omnia fluoroscopic X-ray systems because the swivel arm holding the monitors may become dislodged from the carrying arm.

    Product
    Uroskop Omnia -fluoroscopic X-ray system Model # 10094910 The Uroskop Omnia is a solid state detector fluoroscopic X-ray system, primarily for urological applications (functional x-ray diagnosis, endourology and minimal invasive urology/surgery).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1143-2019·2019-03-13

    Meijer Recalls Chocolate Mint Chip Cookies Due to Undeclared Soy

    Meijer is recalling specific lots of Ultimate Chocolate Mint Chip Cookies because they contain undeclared soy. The recall covers products sold in Meijer stores nationwide.

    Product
    Meijer Ultimate Chocolate Mint Chip Cookie Cookies in clear plastic clamshell 12 count UPC 4125014563 20 count UPC 4125014564
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1225-2019·2019-03-13

    Marketside Butternut Squash Cubes Recalled Due to Listeria Risk

    Southern Specialties, Inc. is recalling Marketside Butternut Squash Cubes because a food contact surface at a supplier facility tested positive for Listeria monocytogenes.

    Product
    Marketside BUTTERNUT SQUASH CUBES 16 OZ (1LB) 454g
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0981-2019·2019-03-13

    BD MAX Enteric Bacterial Panel Recalled for False Negative Results

    Becton Dickinson is recalling 1,583 BD MAX Enteric Bacterial Panel kits due to false negative results for specific bacterial targets.

    Product
    BD MAX Enteric Bacterial Panel -For In Vitro Diagnostic Use with the BD MAX System Catalog Number: 442963 The BD MAX Enteric Bacterial Panel performed on the BD MAX System is an automated in vitro diagnostic test for the direct qualitative detection and differentiation of ent
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V198000·2019-03-13

    TCI Recalls 2015 and 2017 Transtech Buses with Wheelchair Lift Defect

    Transportation Collaborative is recalling 2015 and 2017 Transtech buses because a wheelchair lift cam may fail, allowing the platform to rise too high and increase injury risk.

    Product
    TRANS TECH — TRANS TECH CST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1138-2019·2019-03-13

    Jansal Valley Dukkah Recalled Due to Glass Contamination

    Friendly Fruit Market is recalling Jansal Valley Dukkah because a customer found a piece of glass in the product.

    Product
    JANSAL VALLEY DUKKAH NET WT 2.5 oz. (71 G). The product is packaged in a circular tin can with a clear lid. UPC: 7 08152 31773 0.
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-1227-2019·2019-03-13

    Southern Specialties Recalls French Beans Due to Listeria Risk

    Southern Specialties, Inc. is recalling French Beans because a supplier's food contact surface tested positive for Listeria monocytogenes.

    Product
    FRENCH BEANS 5LBS and FRENCH BEANS 1 LB
    Category
    Food
    Distribution
    0 states
  • HighCPSC·19080·2019-03-13

    H-E-B Recalls Sauté Pans Due to Glass Lid Laceration Hazard

    H-E-B is recalling Kitchen & Table 5.5 qt. Sauté Pans because the glass lids can crack or shatter, posing a laceration hazard.

    Product
    Kitchen & Table 5.5 qt. Sauté Pan with glass lid
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1224-2019·2019-03-13

    Marketside Green Beans Recalled Due to Listeria Contamination Risk

    Southern Specialties, Inc. is recalling Marketside Green Beans because a supplier's food contact surface tested positive for Listeria monocytogenes.

    Product
    Marketside GREEN BEANS NET WT 12 OZ (340g) and Marketside GREEN BEANS NET WT 32 OZ (2 LB) 907g
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1140-2019·2019-03-13

    Schwan's Big Daddy's Bold Cheese Pizza Recalled for Plastic Contamination

    Schwan's is recalling Big Daddy's Bold Cheese Pizza because it may contain plastic pieces. The product was distributed to institutional customers in 23 states.

    Product
    Big Daddy s Bold Cheese Pizza, item No. 78985. 3-Pack. Contains 9-44.53 oz. Pizzas. Net Wt. 25.04 Lbs. (11.36 kg) For Institutional Use. Cook Before Serving. Keep Frozen. Manufactured by: SPC Global Supply Chain, Inc. Marshall, MN 56258
    Category
    Food
    Distribution
    23 states
  • HighFDA (Devices)·Z-0974-2019·2019-03-13

    Draeger Infinity Delta Patient Monitors Recalled for Cybersecurity Vulnerabilities

    Draeger Medical Systems is recalling Infinity Delta patient monitors due to cybersecurity vulnerabilities that may cause device reboots or loss of functionality.

    Product
    Infinity Delta Family patient monitors The Infinity Delta Series (Delta/Delta XL/Kappa) monitors are intended to be used on adult, pediatric, and neonatal populations, with the exception of the parameter Cardiac Output, ST Segment Analysis, and arrhythmia which are intended fo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0973-2019·2019-03-13

    Stryker Reprocessed Arthroscopic Shavers Recalled for Display and Function Errors

    Stryker is recalling 14,265 reprocessed arthroscopic shavers that may display incorrect settings or error messages, preventing proper use during surgery.

    Product
    Stryker Sustainability Solutions (SSS) reprocessed Arthroscopic Shavers Arthroscopic shavers can be used to abrade, cut and excise tissue and bone; remove loose fragments; and, shave away debris in arthroscopic surgeries, as well as surgeries of the jaw and sinuses. Intended
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0970-2019·2019-03-13

    Pentax C2 CryoBalloon Controller Recalled for Overpressure Detection Failure

    Pentax of America Inc is recalling 45 C2 CryoBalloon Controllers because the device fails to detect balloon overpressure during specific nitrous oxide applications, posing a risk of patient injury.

    Product
    C2 CryoBalloon Controller, REF: FG-1017, with Controller Software v1.18.258 The C2 CryoBalloon Ablation System is intended to be used as a cryosurgical tool in the field of general surgery, specifically for endoscopic application and the ablation of dysplastic Barrett s Esopha
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0865-2019·2019-03-13

    Raindrop Near Vision Inlay Recalled Due to Increased Risk of Corneal Haze

    RVO 2.0, Inc. is recalling Raindrop Near Vision Inlays because a post-approval study found an increased risk of corneal haze following implantation.

    Product
    Raindrop Near Vision Inlay, REF: RD1-1, Sterile, Rx Only, Manufacturer ReVision Optics, Inc.
    Category
    Medical Device
    Distribution
    37 states
  • HighFDA (Devices)·Z-0975-2019·2019-03-13

    Draegar Medical Systems Recalls Omega Patient Monitor Software

    Draegar Medical Systems is recalling Omega patient monitor software due to cybersecurity vulnerabilities that may cause device reboots or loss of functionality.

    Product
    Omega Systems These devices are intended to be used in the environment where patient care is provided by Healthcare Professionals, i.e. Physicians, Nurses, and Technicians, who will determine when use of the device is indicated, based upon their professional assessment of the
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0983-2019·2019-03-13

    Maquet Cardiovascular Recalls AXIUS Blower Mister Due to CO2 Flow Issues

    Maquet Cardiovascular is recalling AXIUS Blower Mister devices because a potential lack of carbon dioxide flow may cause procedural delays during off-pump coronary artery bypass surgery.

    Product
    AXIUS Blower Mister Product Code/REF Number: CB-1000 The Axius Blower Mister is intended to clear an anastomotic site for improved visibility
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1145-2019·2019-03-13

    Concord Foods Recalls Salsa Seasoning Mix for Undeclared Milk Allergen

    Concord Foods is recalling Mild Salsa Seasoning Mix packets because they contain undeclared milk, a major food allergen.

    Product
    Concord Fresh Success Mild Salsa Seasoning Mix, Packaged in a NET WT 1.05 OZ (30g) packet, UPC: 0 4140900229 5
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0985-2019·2019-03-13

    Siemens Uroskop Omnia Max Fluoroscopic X-ray System Recall for Swivel Arm Defect

    Siemens is recalling 191 Uroskop Omnia Max fluoroscopic X-ray systems because the swivel arm holding the monitors may become dislodged from the carrying arm.

    Product
    Uroskop Omnia Max -fluoroscopic X-ray system Model # 10762473 Uroskop Omnia Max is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0971-2019·2019-03-13

    Abbott Recalls Architect Magnesium Assay Due to Depressed Urine Results

    Abbott is recalling Architect Magnesium assays because urine tests may show falsely low results. The recall covers 24,995 units distributed in the US and four other countries.

    Product
    ARCHITECT MAGNESIUM, (a) REF 7D70-21, (b) 7D70-31 The Magnesium assay is used for the quantitation of magnesium in human serum, plasma, or urine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1142-2019·2019-03-13

    WTRMLN WTR Cold Pressed Watermelon Juice Recalled for Plastic Contamination

    World Waters is recalling 277,230 units of WTRMLN WTR Cold Pressed Watermelon Juice due to potential soft plastic contamination.

    Product
    Watermelon, WTRMLNWTR Cold Pressured, 12fl oz, Watermelon Flavor, Refrigerated
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1066-2019·2019-03-13

    Ascend Recalls Tamsulosin Hydrochloride Capsules Due to Dissolution Failure

    Ascend Laboratories is recalling 3,072 bottles of Tamsulosin Hydrochloride 0.4 mg capsules because stability testing revealed high out-of-specification dissolution results.

    Product
    TAMSULOSIN HYDROCHLORIDE — TAMSULOSIN HYDROCHLORIDE (TAMSULOSIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1152-2019·2019-03-13

    Gasco Golden Egg Yellow Food Color Recalled for Undeclared Ingredients

    Gasco Industrial is recalling Golden Egg Yellow Shade Food Color because the label fails to declare Yellow #5 and potassium sorbate.

    Product
    Gasc¿ Golden Egg Yellow Shade Food Color, Contains: 32 fl. oz. (946 mL)
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0980-2019·2019-03-13

    Stryker Recalls T2 Basic Long Instrument Sets Due to Mislabeling

    Stryker GmbH is recalling 17 T2 Basic Long Instrument Sets because faceplates may incorrectly identify them as T2 Basic Short sets.

    Product
    Instrument Tray, Basic T2 Femur Long Catalog #: 1806-9900 Product Usage: Knee Arthroplasty
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Food)·F-1146-2019·2019-03-13

    Good Neighbor Pharmacy Co Q10 Capsules Recalled for Mislabeling

    Twenty-First Century Healthcare is recalling Good Neighbor Pharmacy Co Q10 200mg capsules because they are mislabeled and may contain Vitamin D.

    Product
    Good Neighbor Pharmacy, Co Q10 200mg Capsule, Dietary Supplement, UPC: 0-87701-40817-5, 30 capsules.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0982-2019·2019-03-13

    Cepheid Respiratory Control Panel Recalled for Reduced Expiration Date

    Microbiologics Inc is recalling Cepheid Respiratory Control Panels because the expiration date was reduced from 24 months to 13 months.

    Product
    Cepheid Respiratory Control Panel Catalog #8199 for in vitro diagnostic use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1153-2019·2019-03-13

    Gasco Tomato Red Food Color Recalled for Undeclared Yellow #6

    Gasco Industrial is recalling Tomato Red Food Color because it fails to declare Yellow #6, a food additive.

    Product
    Gasc¿ Tomato Red Food Color, Net Contents: 5 gal (640 fl. oz)
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0972-2019·2019-03-13

    Zimmer Biomet Recalls Reverse Shoulder Baseplates Due to Missing Adapter

    Zimmer Biomet is recalling 52 Comprehensive Reverse Shoulder System Glenosphere Mini Baseplates that may be missing a taper adapter.

    Product
    Comprehensive Reverse Shoulder System Glenosphere Mini Baseplate with Taper Adapter, Model Number 010000589 Biomet Comprehensive Reverse Shoulder products are indicated for use in patients whose shoulder joint has a grossly deficient rotator cuff with severe arthropathy and/o
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0992-2019·2019-03-13

    Apotex Recalls Out-of-Sequence Contraceptive Tablets

    Apotex Inc. is recalling specific lots of Drospirenone and Ethinyl Estradiol tablets because they may be missing or placed incorrectly in the blister pack.

    Product
    Drospirenone and Ethinyl Estradiol Tablets, USP, 3 mg/0.03 mg, 28 Tablets Blister, 1 Unit (NDC 60505-4183-1) packaged as 84 Tablets Blister, 3x1 Unit per carton (NDC 60505-4183-3), Rx Only, Manufactured for: Apotex Corp., Weston, FL 33326; Manufactured by: Oman Pharmaceutical Pr
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1147-2019·2019-03-13

    Good Neighbor Pharmacy Vitamin D Supplement Recalled for Mislabeling

    Twenty-First Century Healthcare is recalling Good Neighbor Pharmacy Vitamin D 2000 IU tablets because they are mislabeled and may contain Co Q10.

    Product
    Good Neighbor Pharmacy, D 2000 IU, Dietary Supplement, UPC: 0-87701-40751-2, 30 tablets.
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0519-2019·2019-03-13

    Jubilant Cadista Recalls Bupropion Hydrochloride Extended-Release Tablets for Dissolution Failure

    Jubilant Cadista Pharmaceuticals is recalling specific lots of Bupropion Hydrochloride Extended-Release Tablets because they failed dissolution specifications at a 9-month stability timepoint.

    Product
    BuPROPion Hydrochloride Extended-Release Tablets, USP (XL) 150 mg, a) 30 count (NDC 59746- 758-30) & b) 90 count (NDC 59746-758-90) bottles, Rx only, Manufactured b Jubilant Generis Ltd, Roorkee, India, Marketed by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD
    Category
    Drug
    Distribution
    0 states
  • LowFDA (Drugs)·D-0994-2019·2019-03-13

    Petra Hygienic Systems Recalls Athleticare Hand Soap Due to Triclosan

    Petra Hygienic Systems is recalling Athleticare Anti-Bacterial Hand Soap because it contains triclosan, an ingredient no longer permitted in over-the-counter antiseptic wash products.

    Product
    ATHLETICARE Anti-Bacterial Hand Soap AC 550 (triclosan), 0.25%, 4 litres/1.1 US Gallon bottles, packaged in 4 x 4 Litres/1.1 US gallons per case, Petra Hygienic Systems, Concord, ON L4K 4RS/ Reno, NV 89511, NDC 42326-550-01, UPC 0 65936 10335 5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·19079·2019-03-12

    HP Recalls Lithium-Ion Batteries for Commercial Notebooks and Workstations

    HP is expanding a recall of lithium-ion batteries for commercial notebook computers and mobile workstations due to fire and burn hazards.

    Product
    Lithium-ion batteries for HP commercial notebook computers and mobile workstations
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·027-2019·2019-03-12

    Carnivore Meat Company Recalls Beef and Pork Sausage Due to Undeclared Soy

    Carnivore Meat Company is recalling approximately 379 pounds of raw beef and pork sausage products because they contain undeclared soy, a known allergen.

    Product
    LSI Specialty Meats — Carnivore Meat Company, LLC Recalls Beef and Pork Sausage Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    2 states
  • HighUSDA FSIS·028-2019·2019-03-12

    North Country Smokehouse Recalls Pork Sausage Due to Gluten Misbranding

    North Country Smokehouse is recalling approximately 9,000 pounds of pork banger sausage because the product contains wheat despite a gluten-free claim.

    Product
    North Country Smokehouse — North Country Smokehouse Recalls Pork Sausage Products Due to Misbranding
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·026-2019·2019-03-11

    Choice Canning Recalls Chicken Fried Rice for Undeclared Milk Allergen

    Choice Canning Company is recalling approximately 35,459 pounds of FUSIA Chicken Fried Rice products because they contain milk, a known allergen, that is not declared on the label.

    Product
    Choice Canning Company Inc. — Choice Canning Company, Inc. Recalls Chicken Fried Rice Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    9 states
  • SevereNHTSA·19E024000·2019-03-11

    Natural Gas Fuel Systems Recalls CNG Fuel Cylinders for Rupture Risk

    Natural Gas Fuel Systems is recalling specific compressed natural gas fuel systems for heavy and medium-duty vehicles because the cylinders may unexpectedly rupture.

    Product
    FUEL SYSTEM, OTHER:STORAGE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V195000·2019-03-11

    Mertz Custom Trailer Recall for Air Brake Plastic Connector Defect

    Mertz is recalling 2008-2018 custom trailers because plastic air brake connectors may fail, potentially causing brake loss or unexpected emergency brake activation.

    Product
    MERTZ — MERTZ CUSTOM TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·025-2019·2019-03-09

    Conagra Recalls Chef Boyardee Bowls Due to Undeclared Allergens and Misbranding

    Conagra Brands is recalling specific Chef Boyardee rice bowls that contain undeclared milk and wheat allergens and are mislabeled as beef ravioli.

    Product
    Hometown Food Company — Conagra Brands, Inc. Recalls Chicken and Rice Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·19V194000·2019-03-08

    SVO Group Recalls 2018 Embassy Buses for Rear Axle Defect

    SVO Group is recalling 2018 Embassy shuttle buses because loose U-bolts may allow the rear axle to separate, increasing crash risk.

    Product
    SVO GROUP — SVO GROUP EMBASSY BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V186000·2019-03-08

    EBY Livestock Trailer Recall for Improperly Greased Axle Bearings

    M H EBY is recalling 2019-2020 EBY Gooseneck Livestock Trailers because inner wheel bearings may not have been properly greased, posing fire and crash risks.

    Product
    EBY — EBY RUFF NECK, MAVERICK, MAVERICK LS, WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19077·2019-03-08

    TJX Recalls Aroma Home USB Heating Pads Due to Fire and Burn Hazards

    TJX is recalling Aroma Home USB Heated Hottie heating pads sold at T.J. Maxx and Marshalls because they can overheat, posing fire and burn risks.

    Product
    Aroma Home USB Heated Hottie heating pads
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V191000·2019-03-08

    Forest River Surveyor Recalled for Incorrect Axle Weight Placard

    Forest River is recalling 2018-2019 Surveyor trailers because the Federal Placard lists 3,500 lb axles instead of the actual 2,500 lb capacity, risking overload and loss of control.

    Product
    FOREST RIVER — FOREST RIVER SURVEYOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V193000·2019-03-08

    Gillig Recalls 2014-2019 Low Floor Buses for Headlight Short Circuit Risk

    Gillig is recalling 2014-2019 Low Floor buses because uncovered electrical terminals in the headlight circuit may short circuit, causing a loss of headlights and increasing crash risk.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V187000·2019-03-07

    Suzuki Recalls Grand Vitara and Kizashi for Air Bag Sensor Issues

    Suzuki is recalling 2006-2013 Grand Vitara and 2010-2013 Kizashi vehicles because the front passenger seat may shrink, causing the air bag sensor to misclassify occupants.

    Product
    SUZUKI — SUZUKI GRAND VITARA, KIZASHI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V189000·2019-03-07

    KME Recalls 2018 Predator TDA Vehicles Due to Waterway Weld Failure

    Kovatch Mobile Equipment is recalling 2018 Predator TDA vehicles because a weld on the waterway pipes may fail, causing pipes to detach and injure nearby people.

    Product
    KME — KME PREDATOR TDA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V184000·2019-03-07

    GM Recalls 2019 Chevrolet Equinox and GMC Terrain for Seat Welds

    General Motors is recalling 2019 Chevrolet Equinox and GMC Terrain vehicles because insufficient welds on the rear-right seat head-restraint bracket may increase injury risk in a crash.

    Product
    CHEVROLET — CHEVROLET, GMC EQUINOX, TERRAIN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1134-2019·2019-03-06

    Whole Foods Veggie Supreme Pizza Recalled for Salmonella Risk

    Whole Foods Market is recalling 20 units of Veggie Supreme Pizza from its hot bar due to potential Salmonella contamination. The product was sold in eight states.

    Product
    Hot Bar Item; Veggie Supreme Pizza
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-1110-2019·2019-03-06

    Whole Foods Turkey Sandwiches Recalled for Salmonella Contamination

    Whole Foods Market is recalling Turkey with Spinach & Feta Sandwiches due to potential Salmonella contamination. The affected products were sold in eight northeastern and southeastern states.

    Product
    Turkey with Spinach & Feta Sandwich packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-1057-2019·2019-03-06

    Puratos Tegral Satin Gold CL Crème Cake Recalled for Undeclared Milk

    Puratos Corporation is recalling Tegral Satin Gold CL Crème Cake because the product contains undeclared milk. The recall affects 25,700 lbs distributed across nine states.

    Product
    Tegral Satin Gold CL Cr¿me Cake, packaged in 50 lb. bag.
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-1111-2019·2019-03-06

    Whole Foods Recalls Chicken Cordon Blue Panini Due to Salmonella Risk

    Whole Foods Market is recalling Chicken Cordon Blue Panini packaged in plastic nonflexible containers due to potential Salmonella contamination. The recall covers specific sell-by dates in eight northeastern and southeastern states.

    Product
    Chicken Cordon Blue Panini packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-1066-2019·2019-03-06

    Ottogi Bulgogi Ramen Recalled for Undeclared Egg Allergen

    Ottogi America is recalling Ppushu Ppushu Bulgogi Flavor ramen due to an undeclared egg allergen. Consumers should stop eating the product.

    Product
    Ottogi Ppushu Ppushu Bulgogi Flavor 3.17oz x 40ea Item #21503005 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states
  • CriticalFDA (Food)·F-1129-2019·2019-03-06

    Whole Foods Recalls Spinach Walnut Bleus Pizza for Salmonella Risk

    Whole Foods Market is recalling Spinach Walnut Bleus Pizza due to potential Salmonella contamination. The product was sold in eight Northeast and Southeast states.

    Product
    Spinach Walnut Bleus Pizza packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-1117-2019·2019-03-06

    Whole Foods Egg White and Spinach Breakfast Recalled for Salmonella

    Whole Foods Market is recalling Egg White and Spinach Breakfast packaged in plastic nonflexible containers due to potential Salmonella contamination.

    Product
    Egg White and Spinach Breakfast packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-1124-2019·2019-03-06

    Whole Foods Turkey Brie Sandwich Baguette Recalled for Salmonella Risk

    Whole Foods Market is recalling Turkey Brie Sandwich Baguettes due to potential Salmonella contamination. The product was sold in eight Northeastern and Southeastern states.

    Product
    Sandwich Baguette Turkey Brie packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-1109-2019·2019-03-06

    Whole Foods Recalls Turkey Avocado Sandwiches Due to Salmonella Risk

    Whole Foods Market is recalling Turkey Avocado Sandwiches (Turkado) in eight states due to potential Salmonella contamination.

    Product
    Turkey Avocado Sandwich (Turkado Sandwich) packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-1085-2019·2019-03-06

    Produce Packaging Inc Recalls Tray Vegetable Packaging Due to E. coli Risk

    Produce Packaging Inc is recalling Tray Vegetable 16" packaging due to potential E. coli contamination. The product was distributed in Ohio, Michigan, New York, and Texas.

    Product
    Produce Packaging, Inc. Tray Vegetable 16"
    Category
    Consumer Product
    Distribution
    4 states
  • CriticalFDA (Food)·F-1115-2019·2019-03-06

    Whole Foods Bistro Pasta Salad Recalled for Salmonella Contamination

    Whole Foods Market is recalling Bistro Pasta Salad packaged in plastic nonflexible containers due to potential Salmonella contamination. The product was distributed in eight northeastern and southeastern states.

    Product
    Bistro Pasta Salad packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-1105-2019·2019-03-06

    Whole Foods Recalls Spring Berry Power Salad Due to Salmonella Risk

    Whole Foods Market is recalling Spring Berry Power salad packaged in plastic nonflexible containers due to potential Salmonella contamination.

    Product
    Salad Spring Berry Power packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-1127-2019·2019-03-06

    Whole Foods Spinach Gorgonzola Salad Recalled for Salmonella Risk

    Whole Foods Market is recalling Spinach Gorgonzola Salad packaged in plastic nonflexible containers due to potential Salmonella contamination.

    Product
    Spinach Gorgonzola Salad packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Devices)·Z-0805-2019·2019-03-06

    ICU Medical Recalls ChemoLock Vial Spike Due to Potential Burr Particulate

    ICU Medical is recalling one lot of ChemoLock Vial Spike devices due to a potential for containing burr particulate. The recall covers 2,050 units distributed in the US and internationally.

    Product
    icumedical ChemoLock Vial Spike, 20mm, REF CL-80S The ChemoLock Closed System Drug Transfer Device prevents the transfer of environmental contaminants, including bacterial and airborne contaminants into the system, and the escape of drug or vapor concentrations outside the sy
    Category
    Medical Device
    Distribution
    7 states
  • CriticalFDA (Food)·F-1113-2019·2019-03-06

    Whole Foods Recalls Paleo Mediterranean Tuna Salad Due to Salmonella Risk

    Whole Foods Market is recalling Paleo Mediterranean Tuna Salad in plastic containers due to potential Salmonella contamination. The product was sold in eight northeastern and southeastern states.

    Product
    Paleo Mediterranean Tuna Salad packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-1120-2019·2019-03-06

    Whole Foods Recalls Goat Cheese Salad Due to Salmonella Risk

    Whole Foods Market is recalling Goat Cheese Salad with Mandarin Orange and Candied Cashews because it may be contaminated with Salmonella.

    Product
    Goat Cheese Salad with Mandarin Orange and Candied Cashews packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-1114-2019·2019-03-06

    Whole Foods Recalls Spinach Sauteed with Garlic Due to Salmonella Risk

    Whole Foods Market is recalling Spinach Sauteed with Garlic packaged in plastic nonflexible containers due to potential Salmonella contamination.

    Product
    Spinach Sauteed with Garlic packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-1106-2019·2019-03-06

    Whole Foods Recalls Spinach and Vegetable Quinoa Salad Due to Salmonella Risk

    Whole Foods Market is recalling Spinach and Vegetable Quinoa Salad packaged in plastic nonflexible containers because the product is potentially contaminated with Salmonella.

    Product
    Spinach and Vegetable Quinoa Salad packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-1136-2019·2019-03-06

    Whole Foods Market Recalls Tofu Soy and Sea Hot Bar Item

    Whole Foods Market is recalling Tofu Soy and Sea hot bar items due to potential Salmonella contamination. The product was sold in eight Northeastern and Southeastern states.

    Product
    Hot Bar Item; Tofu Soy and Sea
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-1125-2019·2019-03-06

    Whole Foods Recalls Serbian Ajvar Vegetable Club Due to Salmonella Risk

    Whole Foods Market is recalling Serbian Ajvar Vegetable Club packaged in plastic nonflexible containers due to potential Salmonella contamination.

    Product
    Serbian Ajvar Vegetable Club packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • CriticalNHTSA·19V182000·2019-03-06

    Honda and Acura Recall Vehicles for Driver Air Bag Inflator Defect

    Honda is recalling specific Acura and Honda vehicles because a manufacturing error in the driver's air bag inflator may cause it to explode during a crash.

    Product
    ACURA — ACURA, HONDA RDX, ILX, CIVIC GX, ZDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0927-2019·2019-03-06

    Philips Achieva 3.0T MRI System Recalled for Ceiling Speaker Hazard

    Philips is recalling Achieva 3.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Achieva 3.0T for PET, Model Number 781477. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0893-2019·2019-03-06

    Philips Achieva 3.0T MRI System Recalled Due to Ceiling Speaker Hazard

    Philips is recalling 11,226 Achieva 3.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Achieva 3.0T, Model Number 781177. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0916-2019·2019-03-06

    Philips Ingenia 1.5T S MRI Systems Recalled for Falling Speaker Hazard

    Philips is recalling Ingenia 1.5T S MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Ingenia 1.5T S, Model Number 781347. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0906-2019·2019-03-06

    Philips Achieva 3.0T MRI System Recalled for Ceiling Speaker Hazard

    Philips is recalling 11,226 Achieva 3.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Achieva 3.0T TX-series, Model Number 781278. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0878-2019·2019-03-06

    Philips MRI System Recall Due to Ceiling Speaker Magnetic Hazard

    Philips is recalling Intera 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Intera 1.5T Power/Pulsar, Model Number 781105. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V172000·2019-03-06

    Jayco Recalls 2018 Fifth Wheel Trailers Due to Fuel Tank Hardware Issue

    Jayco is recalling 2018 Talon and Seismic fifth wheel trailers because incorrect hardware may fail to secure the auxiliary fuel tank, increasing the risk of a fire.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL TALON, SEISMIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0915-2019·2019-03-06

    Philips Achieva 1.5T MRI System Recalled for Falling Speaker Hazard

    Philips is recalling 11,226 Achieva 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Achieva 1.5T Conversion, Model Number 781346. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide

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