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.

801–900 of 999

  • SevereNHTSA·19V181000·2019-03-06

    Karma Recalls 2012 Fisker Karma Vehicles for Air Bag Inflator Defect

    Karma Automotive is recalling 2012 Fisker Karma vehicles because passenger frontal air bag inflators may explode due to propellant degradation, posing a risk of serious injury or death.

    Product
    FISKER — FISKER KARMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0901-2019·2019-03-06

    Philips Ingenia MRI System Recalled Due to Ceiling Speaker Hazard

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

    Product
    Ingenia 1.5T CX, Model Number 781261. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V179000·2019-03-06

    Porsche Recalls 2018 Models for Loose Side Air Bag Sensors

    Porsche is recalling 417 vehicles because side air bag impact sensors may not be properly tightened, which could prevent air bag deployment in a crash.

    Product
    PORSCHE — PORSCHE 911, 718 BOXSTER, 718 CAYMAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V178000·2019-03-06

    Entegra Recalls 2019-2020 Reatta Motorhomes for Damaged Tow Hitch

    Entegra Coach is recalling 2019-2020 Reatta motorhomes because the tow hitch may have been damaged during delivery, increasing the risk of a crash.

    Product
    ENTEGRA — ENTEGRA REATTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1121-2019·2019-03-06

    Whole Foods Market Recalls Large Goat Cheese Green Salad for Salmonella Risk

    Whole Foods Market is recalling Large Goat Cheese Green Salad due to potential Salmonella contamination. The product was sold in eight northeastern and southeastern states.

    Product
    Large Goat Cheese Green Salad packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·F-1128-2019·2019-03-06

    Whole Foods Spinach Strawberry Goat Cheese Salad Recalled for Salmonella Risk

    Whole Foods Market is recalling Spinach Strawberry Goat Cheese Salad due to potential Salmonella contamination. The product was sold in eight northeastern and southeastern states.

    Product
    Spinach Strawberry Goat Cheese Salad packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·F-1091-2019·2019-03-06

    Produce Packaging Inc. Recalls Stir-Fry Mix Due to E. coli Risk

    Produce Packaging Inc. is recalling 525 units of 9 LB Stir-Fry Mix due to potential E. coli contamination. The product was distributed in Ohio, Michigan, New York, and Texas.

    Product
    Produce Packaging, Inc. Mix, Stir-Fry WG 9 LB
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1130-2019·2019-03-06

    Whole Foods Recalls Pesto Greens for Salmonella Risk

    Whole Foods Market is recalling Hot Bar Item; Pasta Pesto Greens due to potential Salmonella contamination. The product was sold in eight northeastern and southeastern states.

    Product
    Hot Bar Item; Pasta Pesto Greens
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-0918-2019·2019-03-06

    Philips Ingenia 3.0T MRI System Recalled for Falling Speaker Hazard

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

    Product
    Ingenia 3.0T, Model Number 781377. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0922-2019·2019-03-06

    Philips Ingenia Elition S MRI System Recalled for Falling Speaker Hazard

    Philips is recalling Ingenia Elition S MRI systems because ceiling speakers may fall due to magnetic attraction.

    Product
    Ingenia Elition S, Model Number 781357. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1116-2019·2019-03-06

    Whole Foods Recalls Breakfast Sandwich Platters Due to Salmonella Risk

    Whole Foods Market is recalling Breakfast Sandwich Platters packaged in plastic nonflexible containers due to potential Salmonella contamination.

    Product
    Breakfast Sandwich Platter packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-0895-2019·2019-03-06

    Philips Intera 1.5T MRI System Recalled for Ceiling Speaker 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, Model Number 781195. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0917-2019·2019-03-06

    Philips Panorama 1.0T MRI Systems Recalled for Falling Speaker Hazard

    Philips is recalling 11,226 Panorama 1.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Panorama 1.0T, Model Number 781350. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1126-2019·2019-03-06

    Whole Foods Recalls Spinach Artichoke Bleus Pizza Due to Salmonella Risk

    Whole Foods Market is recalling Spinach Artichoke Bleus Pizza packaged in plastic nonflexible containers because the product is potentially contaminated with Salmonella.

    Product
    Spinach Artichoke Bleus Pizza packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·F-1112-2019·2019-03-06

    Whole Foods Recalls New England Cranberry Turkey Sandwiches for Salmonella Risk

    Whole Foods Market is recalling New England Cranberry Turkey Sandwiches due to potential Salmonella contamination. The products were sold in eight northeastern and southeastern states.

    Product
    New England Cranberry Turkey Sandwich packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-0884-2019·2019-03-06

    Philips Achieva XR MRI Systems Recalled for Ceiling Speaker Hazard

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

    Product
    Achieva XR 1.5T/3.0T, Model Number 781153. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0873-2019·2019-03-06

    Philips Multiva MRI System Recalled Due to Ceiling Speaker Hazard

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

    Product
    Multiva 1.5T 16 R5, Model Number 781078. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0926-2019·2019-03-06

    Philips MR RT MRI Systems Recalled for Falling Ceiling Speaker Hazard

    Philips is recalling MR RT MRI systems because ceiling speakers may fall due to magnetic attraction.

    Product
    MR RT, Model Number 781439. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0885-2019·2019-03-06

    Philips Intera IT MRI Systems Recalled for Falling Ceiling Speaker Risk

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

    Product
    Intera IT, Model Number 781160. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V177000·2019-03-06

    Jayco Recalls 2019-2020 Embark Motorhomes Due to Hitch Damage

    Jayco is recalling 2019-2020 Embark motorhomes because the hitch may have been damaged during delivery, increasing the risk of a crash if the towed vehicle separates.

    Product
    JAYCO — JAYCO EMBARK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1107-2019·2019-03-06

    Whole Foods Spinach Ravioli Salad Recalled for Salmonella Risk

    Whole Foods Market is recalling Spinach Ravioli Salad with Lemon, Tomato, and Parmesan due to potential Salmonella contamination.

    Product
    Spinach Ravioli Salad with Lemon, Tomato, and Parmesan packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-0907-2019·2019-03-06

    Philips Achieva MRI System Recalled for Falling Ceiling Speaker Hazard

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

    Product
    Achieva 1.5T Conversion, Model Number 781283. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0888-2019·2019-03-06

    Philips MRI System Recall Due to Ceiling Speaker Magnetic Hazard

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

    Product
    Intera Achieva 1.5T Nova, Model Number 781172. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0876-2019·2019-03-06

    Philips Intera 1.0T MRI System Recalled for Ceiling Speaker Hazard

    Philips is recalling Intera 1.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Intera 1.0T Power/Pulsar, Model Number 781103. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0886-2019·2019-03-06

    Philips Intera 1.5T MRI Systems Recalled for Falling Speaker Hazard

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

    Product
    Intera 1.5T R11, Model Number 781170. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1122-2019·2019-03-06

    Whole Foods Spinach and Mushroom Salad Recalled for Salmonella Risk

    Whole Foods Market is recalling Large and Small Spinach and Mushroom Salads due to potential Salmonella contamination. The products were sold in eight northeastern and southeastern states.

    Product
    Large Spinach and Mushroom Salad and Small Spinach and Mushroom Salad packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • SevereNHTSA·19V188000·2019-03-06

    Volkswagen Recalls 56,173 Vehicles for Rear Coil Spring Fracture Risk

    Volkswagen is recalling 56,173 vehicles because rear coil springs may fracture prematurely, potentially causing tire damage and loss of vehicle control.

    Product
    VOLKSWAGEN — VOLKSWAGEN TIGUAN, GOLF SPORTWAGEN, GOLF, JETTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0923-2019·2019-03-06

    Philips Ingenia Elition X MRI Systems Recalled for Falling Speaker Hazard

    Philips is recalling Ingenia Elition X MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Ingenia Elition X, Model Number 781358. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1104-2019·2019-03-06

    Whole Foods Quinoa with Dark Leafy Greens Recalled for Salmonella Risk

    Whole Foods Market is recalling Quinoa with Dark Leafy Greens due to potential Salmonella contamination. The product was sold in eight northeastern and southeastern states.

    Product
    Quinoa with Dark Leafy Greens packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-0924-2019·2019-03-06

    Philips MR-OR 1.5T MRI Systems Recalled for Falling Speaker Hazard

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

    Product
    MR-OR 1.5T, Model Number 781437. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1103-2019·2019-03-06

    Whole Foods Mediterranean Stuffed Salmon Recalled for Salmonella Risk

    Whole Foods Market is recalling Mediterranean Stuffed Salmon in plastic containers due to potential Salmonella contamination. The product was sold in eight Northeastern and Southeastern states.

    Product
    Mediterranean Stuffed Salmon packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-0965-2019·2019-03-06

    Elekta Recalls Monaco Radiation Treatment Planning System Software

    Elekta, Inc. is recalling 14 Monaco Radiation Treatment Planning System devices due to a software defect that may cause incorrect optimization models to be used during online plan adaptation.

    Product
    Monaco Radiation Treatment Planning (RTP) System
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-0913-2019·2019-03-06

    Philips Achieva 3.0T X MRI Systems Recalled for Falling Speaker Hazard

    Philips is recalling 11,226 Achieva 3.0T X MRI systems because ceiling speakers may fall due to the magnetic field.

    Product
    Achieva 3.0T X, Model Number 781344. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0910-2019·2019-03-06

    Philips Ingenia 1.5T MRI System Recalled for Ceiling Speaker Hazard

    Philips is recalling Ingenia 1.5T MRI systems because ceiling speakers may fall due to magnetic attraction.

    Product
    Ingenia 1.5T, Model Number 781341. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1073-2019·2019-03-06

    Ottogi Buckwheat Chilli Noodles Recalled for Undeclared Egg Allergen

    Ottogi America is recalling Buckwheat Chilli Noodles because they contain egg, which is not listed on the label.

    Product
    Ottogi BuckwheatChilli Noodle PK 1lb 6.93oz x 8pk Item #32143061 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states
  • HighNHTSA·19V168000·2019-03-06

    Highland Ridge RV Recalls 2019 Travel Trailers Due to Incorrect Weight Label

    Highland Ridge RV is recalling 74 units of 2019 Mesa Ridge and Open Range Ultra Lite travel trailers because the weight label exceeds the safety chain rating.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT OPEN RANGE ULTRA LITE, MESA RIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0911-2019·2019-03-06

    Philips Ingenia 3.0T MRI Systems Recalled for Ceiling Speaker Hazard

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

    Product
    Ingenia 3.0T, Model Number 781342. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1108-2019·2019-03-06

    Whole Foods Recalls Smoked Turkey Sandwiches for Salmonella Risk

    Whole Foods Market is recalling smoked turkey sandwiches in eight states due to potential Salmonella contamination.

    Product
    Smoked Turkey with Apple & Cheddar Sandwich packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-0892-2019·2019-03-06

    Philips MRI System Recall Due to Falling Ceiling Speaker Hazard

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

    Product
    Intera Achieva 1.5T IT Nova Dual, Model Number 781176. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1064-2019·2019-03-06

    Ottogi Jjajang Bokki Noodles Recalled for Undeclared Egg Allergen

    Ottogi America is recalling Jjajang Bokki noodle bowls because they contain egg, which is not listed on the label.

    Product
    Ottogi Jjajang Bokki (Bowl) 4.23oz x 12ea Item #21502157 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-0929-2019·2019-03-06

    Philips Ingenia 1.5T MRI System Recalled for Falling Speaker Hazard

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

    Product
    NZM101 Ingenia 1.5T Linac, Model Number 781483. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1063-2019·2019-03-06

    Ottogi Snack Ramen Recalled for Undeclared Egg Allergen

    Ottogi America is recalling specific lots of Ottogi Snack Ramen cups because they contain egg, which is not listed on the label.

    Product
    Ottogi Snack Ramen 5PK, Cup 1lb 3.05oz x 8pk, 2.18oz x 6ea Item #21501281, 21502161 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·F-1089-2019·2019-03-06

    Produce Packaging Inc Recalls Stir Fry Mix Due to E. coli Risk

    Produce Packaging Inc is recalling Stir Fry #6 mix because of a potential E. coli contamination identified by a supplier.

    Product
    Produce Packaging, Inc. Mix, Stir Fry #6 6/10 OZ
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1087-2019·2019-03-06

    Produce Packaging Inc. Recalls Cauliflower Florets Due to E. coli Risk

    Produce Packaging Inc. is recalling Cauliflower, Floret 4/3 LB due to potential E. coli contamination. The product was distributed in Ohio, Michigan, New York, and Texas.

    Product
    Produce Packaging, Inc. Cauliflower, Floret 4/3 LB
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-0956-2019·2019-03-06

    Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Leaks

    Arrow International Inc. is recalling Arrow AutoFuser Disposable Pain Control Pumps due to possible cracks on the fill port connector that may cause leaks and reduced drug delivery.

    Product
    AF w/AS 550 x 1-14ML/HR 5ML-60LO CPNB, Product code MVBX60XL CPNB, Arrow AutoFuser Disposable Pain Control Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1060-2019·2019-03-06

    Ottogi Ramen Bokki Cup Noodles Recalled for Undeclared Egg Allergen

    Ottogi America is recalling 1.6 million units of Ramen Bokki cup noodles due to an undeclared egg allergen. Consumers should stop eating the product.

    Product
    Ottogi Ramen Bokki (Cup) 4.23oz x 12ea Item #21309009 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-0875-2019·2019-03-06

    Philips MRI Systems Recalled Due to Ceiling Speaker Fall Risk

    Philips is recalling Intera 1.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Intera 1.0T Omni/Stellar, Model Number 781102. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0883-2019·2019-03-06

    Philips Intera 3.0T MRI System Recalled for Ceiling Speaker Hazard

    Philips is recalling Intera 3.0T MRI systems because ceiling speakers may fall due to magnetic attraction.

    Product
    Intera 3.0T Master/Quasar Dual, Model Number 781150. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1062-2019·2019-03-06

    Ottogi Jin Ramen Spicy Bowl Recalled for Undeclared Egg Allergen

    Ottogi America Inc. is recalling specific lots of Ottogi Jin Ramen Spicy Bowl due to an undeclared egg allergen. Consumers should check their pantry and stop eating the product.

    Product
    Ottogi Jin Ramen Spicy, Bowl, 5PK 4.23oz x 20ea, 3.88oz x 12ea, 1lb 5.16oz x 8pk Item #21501202, 21502155, 32142402 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·F-1092-2019·2019-03-06

    Produce Packaging Inc. Recalls Veggie Rice Blend Due to E. coli Risk

    Produce Packaging Inc. is recalling 10 LB Veggie Rice Blend products due to potential E. coli contamination. The products were distributed in Ohio, Michigan, New York, and Texas.

    Product
    Produce Packaging, Inc. Mix, Veggie Rice Blend, 10 LB
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1123-2019·2019-03-06

    Whole Foods Market Recalls Mesclun Mix Due to Salmonella Contamination

    Whole Foods Market is recalling Mesclun Mix With Candied Pecans and Sun Dried Cranberries due to potential Salmonella contamination. The product was distributed in eight northeastern and southeastern states.

    Product
    Mesclun Mix With Candied Pecans and Sun Dried Cranberries packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-0896-2019·2019-03-06

    Philips Achieva MRI System Recalled for Falling Ceiling Speaker Hazard

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

    Product
    Achieva 1.5T High Performance, Model Number 781196. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V180000·2019-03-06

    Porsche Recalls 2018 Panamera Models Due to Electrical Control Unit Defect

    Porsche is recalling 2018 Panamera models because incorrect soldering on a control unit may cause intermittent system failures and impaired driveability.

    Product
    PORSCHE — PORSCHE PANAMERA TURBO SPORT TURI, PANAMERA 4S EXECUTIVE, PANAMERA TURBO S HYBRID E, PANAMERA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1069-2019·2019-03-06

    Ottogi Ppushu Ppushu Spicy Flavor Noodles Recalled for Undeclared Egg

    Ottogi America is recalling Ppushu Ppushu Spicy Flavor noodles because they contain egg, which is not listed on the label.

    Product
    Ottogi Ppushu Ppushu Spicy Flavor 3.17oz x 40ea Item #21503008 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-0869-2019·2019-03-06

    Philips Prodiva CS MRI System Recalled for Falling Speaker Hazard

    Philips is recalling Prodiva CS MRI systems because ceiling speakers may fall due to the magnetic field.

    Product
    Prodiva CS, Model Number 781069. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1070-2019·2019-03-06

    Ottogi Beijing JJajang Noodle Recalled for Undeclared Egg Allergen

    Ottogi America is recalling Beijing JJajang Noodles because the product contains egg, which is not declared on the label.

    Product
    Ottogi Beijing JJajang Noodle 5PK 1lb 7.81oz x 8pk Item #32142407 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-0903-2019·2019-03-06

    Philips MRI System Recall Due to Ceiling Speaker Fall Risk

    Philips is recalling SmartPath to dStream MRI systems because ceiling speakers may fall due to magnetic attraction.

    Product
    SmartPath to dStream for XR and 3.0T, Model Number 781270. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0945-2019·2019-03-06

    Arrow AutoFuser Pain Control Pump Recalled for Potential Cracks

    Arrow International is recalling specific AutoFuser Disposable Pain Control Pumps due to possible cracks on the fill port connector that may cause leaks and reduced drug delivery.

    Product
    AF 550 x 5ML/H 6" CATH, 4.5" IN, Product code MC0050XLSK5 CP, Arrow AutoFuser Disposable Pain Control Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1090-2019·2019-03-06

    Produce Packaging Inc Recalls Combo Stir Fry Fajita Packs Due to E. coli Risk

    Produce Packaging Inc is recalling Combo, Stir Fry/Fajita 6 PK products due to potential E. coli contamination. The products were distributed in Ohio, Michigan, New York, and Texas.

    Product
    Produce Packaging, Inc. Combo, Stir Fry/Fajita 6 PK
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-0939-2019·2019-03-06

    Merge Eye Station Retinal Imager Recalled for Electrical Safety Defects

    Merge Healthcare is recalling 1,252 WinStation Retinal Imagers because certain configurations may produce electrical output exceeding allowable medical device limits.

    Product
    The WinStation Retinal Imager, also known as Merge Eye Station. DCF-1024 & DCF-512 Digital Imaging System Product Usage: The WinStation Retinal Imager has the same intended use as other fundus cameras. It is specifically used to produce color or black and white images of the
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0961-2019·2019-03-06

    Alcon Ophthalmic Microscope Recalled for Potential Optical Head Detachment

    Alcon is recalling LuxOr E71 and E71 Q-Vue ophthalmic microscopes because the optical head may detach from the stand due to missing thread adhesive.

    Product
    Alcon or Endure Ophthalmic Microscope Product Usage: Used for low magnification visualization during ophthalmic surgical procedures for cataract, retina and cornea.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0931-2019·2019-03-06

    Philips Multiva MRI System Recalled Due to Ceiling Speaker Hazard

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

    Product
    Multiva 1.5T 8 R5, Model Number 781074. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0943-2019·2019-03-06

    Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Leaks

    Arrow International is recalling specific AutoFuser pumps due to possible cracks in the fill port connector that may cause leaks and reduced drug delivery.

    Product
    AF550x5ML/H 2ML 60LO 6" DUAL CATHS, 4.5", Product MT5060XLYK5 CP, Arrow AutoFuser Disposable Pain Control Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0880-2019·2019-03-06

    Philips Intera 1.5T MRI System Recalled for Falling Speaker 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 CV, Model Number 781107. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0948-2019·2019-03-06

    Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Cracks

    Arrow International is recalling specific AutoFuser pumps due to possible cracks in the fill port connector that could cause leaks and reduced drug delivery.

    Product
    AF 550 x 5ML/HR 2ML 60LO CPNB, Product code MT5060XL CPNB, Arrow AutoFuser Disposable Pain Control Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0952-2019·2019-03-06

    Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Cracks

    Arrow International is recalling 26 units of the AutoFuser Disposable Pain Control Pump due to possible cracks on the fill port connector that may cause leaks.

    Product
    AF w/AS 550 x 0.5-7 ml,w/Y site,DL CPNB, Product code MVAXL2Y CPNB, Arrow AutoFuser Disposable Pain Control Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1065-2019·2019-03-06

    Ottogi Spicy Seafood Udon Noodles Recalled for Undeclared Egg Allergen

    Ottogi America is recalling 1.59 million units of Spicy Seafood Flavor Udon Odongtong bowls due to an undeclared egg allergen.

    Product
    Ottogi Spicy Seafood Flavor Udon Odongtong (Bowl) 3.53oz x 12ea Item #21502162 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-0897-2019·2019-03-06

    Philips Achieva 7.0T MRI System Recalled for Falling Speaker Hazard

    Philips is recalling 11,226 Achieva 7.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Achieva 7.0T, Model Number 781240. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0944-2019·2019-03-06

    Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Cracks

    Arrow International Inc is recalling specific Arrow AutoFuser Disposable Pain Control Pumps due to possible cracks on the fill port connector that may cause leaks and reduced drug delivery.

    Product
    0F 550 x 8ML/HR 2ML 60LO CPNB, Product code MT8060XL CPNB, Arrow AutoFuser Disposable Pain Control Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0866-2019·2019-03-06

    Zimmer Biomet Recalls Vitality Spinal Fixation Set Screws

    Zimmer Biomet is recalling Vitality Shear-off Set Screws because they do not thread properly with mating components due to a manufacturing issue.

    Product
    Vitality¿ Spinal Fixation System. Thoracolumbosacral pedicle screw system (non-sterile). Pedicle screw fixation is indicated for skeletally mature patients and for adolescent patients. For use in Orthopedic medical specialty area. Product Usage: The Vitality Shear-off Set Screw i
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0950-2019·2019-03-06

    Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Leaks

    Arrow International is recalling specific AutoFuser pumps due to possible cracks in the fill port connector that may cause leaks and reduced drug delivery.

    Product
    AF 550 x 8ML/HR 2ML 15LO CPNBMT8015XL CP, Product code MT8015XL CPNB, Arrow AutoFuser Disposable Pain Control Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1059-2019·2019-03-06

    Ottogi Yeul Ramen Bowl Recall for Undeclared Egg Allergen

    Ottogi America is recalling 1,594,338 units of Ottogi Yeul Ramen (Bowl) because the product contains egg, which is not declared on the label.

    Product
    Ottogi Yeul Ramen (Bowl) 4.06oz x 12ea Item #21305007 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·F-1077-2019·2019-03-06

    Produce Packaging Inc. Recalls Rice Cauliflower Due to E. coli Risk

    Produce Packaging Inc. is recalling 5 LB packages of Rice Cauliflower due to potential E. coli contamination. The product was distributed in Ohio, Michigan, New York, and Texas.

    Product
    Produce Packaging, Inc. Cauliflower, Rice 5 LB
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-0942-2019·2019-03-06

    Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Cracks

    Arrow International Inc. is recalling 8 units of the Arrow AutoFuser Disposable Pain Control Pump due to possible cracks on the fill port connector that may cause leaks.

    Product
    AF550x5ML/H 2ML 60LO 6" CATH, 4.5" IN, Product code MT5060XLSK5 CP, Arrow AutoFuser Disposable Pain Control Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0899-2019·2019-03-06

    Philips Achieva XR MRI Systems Recalled for Falling Speaker Hazard

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

    Product
    Achieva XR 1.5T/3.0T , Model Number 781253. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0949-2019·2019-03-06

    Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Cracks

    Arrow International Inc. is recalling 9 units of the Arrow AutoFuser Disposable Pain Control Pump due to possible cracks on the fill port connector that may cause leaks.

    Product
    AF 550 x 5ML/HR CPNB, Product code MC0050XL CPNB, Arrow AutoFuser Disposable Pain Control Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0947-2019·2019-03-06

    Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Cracks

    Arrow International is recalling specific AutoFuser pumps due to possible cracks in the fill port connector that could cause leaks and reduced drug delivery.

    Product
    AF 550 x 5ML/H FH DL 30hole SAT C,4"IN, Product code MC0050XLYK2 CP, Arrow AutoFuser Disposable Pain Control Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0908-2019·2019-03-06

    Philips Intera 1.5T MRI System Recalled for Ceiling Speaker 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 High Performance, Model Number 781295. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1074-2019·2019-03-06

    Ottogi Spicy Seafood Noodles Recalled for Undeclared Egg Allergen

    Ottogi America is recalling Jin Jjambbong Spicy Seafood Noodles because they contain egg, which is not listed on the label.

    Product
    Ottogi Jin Jjambbong Spicy Seafood Noodle 4.58 oz x 4 ea Item #32142443 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-0928-2019·2019-03-06

    Philips Achieva 3.0T MRI System Recalled for Falling Speaker Hazard

    Philips is recalling 11,226 Achieva 3.0T MRI systems because ceiling speakers may fall due to magnetic attraction.

    Product
    Achieva 3.0T TX for PET, Model Number 781479. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0919-2019·2019-03-06

    Philips Ingenia 1.5T MRI Systems Recalled for Falling Speaker Hazard

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

    Product
    Ingenia 1.5T, Model Number 781396. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0890-2019·2019-03-06

    Philips MRI System Recall Due to Ceiling Speaker Fall Risk

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

    Product
    Intera 1.5T Achieva CV Nova, Model Number 781174. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1058-2019·2019-03-06

    Ottogi Ramen Sari Recalled for Undeclared Egg Allergen

    Ottogi America is recalling 1.6 million units of Ramen Sari noodles due to an undeclared egg allergen. The product was distributed in 12 U.S. states and Canada.

    Product
    Ottogi Ramen Sari (Extra Noodle) 3.88oz x 48ea Item #21101009 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·F-1068-2019·2019-03-06

    Ottogi Ppushu Ppushu BBQ Flavor Noodles Recalled for Undeclared Egg Allergen

    Ottogi America Inc. is recalling Ppushu Ppushu BBQ Flavor noodles due to an undeclared egg allergen. Consumers should stop using the product and return it to the store of purchase.

    Product
    Ottogi Ppushu Ppushu BBQ Flavor 3.17oz x 40ea Item #21503007 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·F-1100-2019·2019-03-06

    Nita Crisp Spelt Bread Cracker Recalled for Undeclared Wheat

    Nita Foods Inc. is recalling Nita Crisp Spelt Bread Crackers because the product contains undeclared wheat, a major food allergen.

    Product
    Nita Crisp Spelt Bread Cracker, 8- & 16-ounce bags, In paper bags with a plastic window and has a re-closable ability and safety sealed. Storage: Ambient & Dry
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-1061-2019·2019-03-06

    Ottogi Jin Ramen Mild Bowl Recalled for Undeclared Egg Allergen

    Ottogi America is recalling specific units of Ottogi Jin Ramen Mild Bowl because the product contains egg, which is not declared on the label.

    Product
    Ottogi Jin Ramen Mild Bowl, 5PK 3.88oz x 12ea, 1 lb 5.16oz x 8pk, 4.23oz x 12ea, cup 2.29 oz x 6 cup Item #21309025, 32142401, 21501201, 32143021 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states

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