The Recall Desk

Archive

March 2018 recalls

766 recalls were announced in March 2018.

What the numbers show

Critical
16
Severe
133
High
275
Moderate
293
Low
49

Of the 766 recalls this month scored against our rubric, 2% are Critical, 17% are Severe.

701–766 of 766

  • ModerateFDA (Devices)·Z-0831-2018·2018-03-07

    Cook Percutaneous Gastrojejunostomy Set Recalled for Backwards Wire Guides

    Cook Inc. is recalling Percutaneous Gastrojejunostomy Sets because wire guides may be loaded backwards into the holder.

    Product
    Percutaneous Gastrojejunostomy Set Product Usage: Intended for the percutaneous placement of a catheter for gastroenteric feeding
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0791-2018·2018-03-07

    Avid Medical Recalls Knee Arthroscopy Kits Due to Foreign Material

    Avid Medical is recalling 24 knee arthroscopy kits because they may contain needles with loose polypropylene foreign material.

    Product
    AVID TruCustom KNEE ARTHROSCOPY PACK convenience kits, Item Code: MADN011-02
    Category
    Medical Device
    Distribution
    10 states
  • ModerateFDA (Food)·F-0845-2018·2018-03-07

    Schmidt Baking Recalls Potato Bread Due to Potential Foreign Material

    Schmidt Baking Co. is recalling potato bread products under various trade names due to a potential foreign material in an ingredient supplied by a vendor.

    Product
    P/L POTATO ( Under the following Trade Names - WHOLE FOOODS, PLAIN BAG, GIANT, HP, SHOPPERS, SHOPRITE, WEIS )
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-0779-2018·2018-03-07

    Alcon Recalls 25+ TOTALPLUS Vitrectomy Pak Due to Probe Mismatch

    Alcon is recalling specific lots of the 25+ TOTALPLUS Vitrectomy Pak because a 23GA probe may be included instead of the required 25GA probe.

    Product
    Custom Pak¿ (Custom Pak in which Alcon 25+¿ TOTALPLUS¿ Vitrectomy Pak is a component.) Includes all necessary items for a core vitrectomy procedure and connects to the CONSTELLATION Vision System.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Food)·F-0861-2018·2018-03-07

    Schmidt Baking Recalls 8 Grain Bread Due to Potential Foreign Material

    Schmidt Baking Co. is recalling 8 Grain bread products because a vendor ingredient is under recall, posing a potential foreign material hazard.

    Product
    8 GRAIN ( Under the following Trade Names - INKEEPER )
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-0711-2018·2018-03-07

    Siemens Axiom Artis Fluoroscopic Foot Switch Recalled for Potential Failure

    Siemens is recalling 142 Axiom Artis fluoroscopic foot switches that may fail to release radiation due to external impacts.

    Product
    Axiom Artis model Interventional fluoroscopic x-ray foot switch accessory; Model Numbers: 4787797, 4787805, and 4787813.
    Category
    Medical Device
    Distribution
    52 states
  • ModerateFDA (Food)·F-0842-2018·2018-03-07

    Schmidt Baking Recalls Bread Products Due to Potential Foreign Material

    Schmidt Baking Co. is recalling various white bread products sold under multiple trade names due to a potential foreign material issue in an ingredient.

    Product
    BNS WHITE ( Under the following Trade Names - Giant, Harvest Pride -Shoprite, Sunbeam, Blueribbon, Shoppers, Weis )
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-0752-2018·2018-03-07

    Steris Recalls Vis-U-All Heat Seal Pouches Due to Ink Migration

    Steris Corporation is recalling Vis-U-All High Temp Heat Seal Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to medical devices.

    Product
    Vis-U-All High Temp 13"x18" Heat Seal Pouch 100 pouches per box; 4 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0847-2018·2018-03-07

    Schmidt Baking Recalls Potato Slammers Bread Due to Foreign Material Risk

    Schmidt Baking Co. is recalling Potato Slammers bread products because a vendor ingredient is under recall, posing a potential foreign material hazard.

    Product
    POTATO SLAMMERS ( Under the following Trade Names - SCHMIDT, WHOLE FOODS, HP, WEIS, PLAIN BAG 12 and 24 PK )
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Food)·F-0871-2018·2018-03-07

    Meijer Yogurt Recalled for Potential Glass Particles

    Meijer Distribution is voluntarily recalling select Greek and Low-fat yogurt products due to a potential risk of small glass particles.

    Product
    Meijer Yogurt Blended Low-fat Blueberry 6 oz.The products are packaged in a plastic cup with a foil seal and a label listing the UPCs.
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-0765-2018·2018-03-07

    Steris Recalls Vis-U-All High Temperature Sterilization Pouches Due to Ink Migration

    Steris Corporation is recalling Vis-U-All High Temperature Sterilization Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to medical devices.

    Product
    Vis-U-All High Temp 10.5"x28" Self Seal Pouch 100 pouches per box; 4 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0799-2018·2018-03-07

    Avid Medical Recalls TruCustom PV Minor Pack Convenience Kits

    Avid Medical is recalling 52 TruCustom PV Minor Pack convenience kits because they may contain needles with loose polypropylene foreign material.

    Product
    AVID TruCustom PV MINOR PACK convenience kits, Item Code: MADN017-02 and MADN017-03
    Category
    Medical Device
    Distribution
    10 states
  • LowFDA (Devices)·Z-0746-2018·2018-03-07

    Steris Recalls Vis-U-All High Temperature Tubing Due to Ink Migration

    Steris Corporation is recalling Vis-U-All High Temperature Tubing because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to medical devices.

    Product
    Vis-U-All High Temperature Tubing 9"x100'. One roll per box; 10 boxes per case 6 rolls/cs Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0744-2018·2018-03-07

    Steris Recalls Vis-U-All High Temperature Sterilization Pouches Due to Ink Migration

    Steris Corporation is recalling Vis-U-All High Temperature Sterilization Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to medical devices.

    Product
    Vis-U-All High Temperature Tubing 4"x100'. One roll per box; 10 boxes per case 10 rolls/cs Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0748-2018·2018-03-07

    Steris Recalls Vis-U-All Heat Seal Pouches Due to Ink Migration

    Steris is recalling Vis-U-All High Temp Heat Seal Pouches because purple ink may migrate onto the pouch exterior or the medical devices inside after steam processing.

    Product
    Vis-U-All High Temp 3"x8" Heat Seal Pouch 200 pouches per box; 5 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is designed…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0747-2018·2018-03-07

    Steris Recalls Vis-U-All High Temperature Sterilization Pouches Due to Ink Migration

    Steris is recalling Vis-U-All High Temperature Sterilization Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to medical devices.

    Product
    Vis-U-All High Temperature Tubing 14"x100'. One roll per box; 10 boxes per case 6 rolls/cs Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0763-2018·2018-03-07

    Steris Recalls Vis-U-All Pouches Due to Ink Migration

    Steris is recalling Vis-U-All High Temp Self Seal Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and ink transfer to devices.

    Product
    Vis-U-All High Temp 13"x18" Self Seal Pouch 100 pouches per box; 4 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0727-2018·2018-03-07

    Keystone Dental Recalls Mislabeled Stage-1 RDS Indexed Abutments

    Keystone Dental Inc is recalling 20 Stage-1 RDS Indexed Abutments because the expiration date on the label is incorrect.

    Product
    Stage-1¿ RDS Indexed Abutment for RDS Stage-1¿ Single Stage Implants Keystone s implants are intended for use in partially or fully edentulous mandibles and maxillae, in support of single or multiple-unit restorations including; cement retained, screw retained, or…
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Devices)·Z-0770-2018·2018-03-07

    Steris Recalls Vis-U-All Pouches Due to Ink Migration Defects

    Steris Corporation is recalling Vis-U-All High Temperature Sterilization Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to medical devices.

    Product
    Vis-U-All High Temp 7.5"x13" Self Seal Pouch 200 pouches per box; 4 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0762-2018·2018-03-07

    Steris Recalls Vis-U-All High Temperature Sterilization Pouches Due to Ink Migration

    Steris Corporation is recalling Vis-U-All High Temperature Sterilization Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to devices.

    Product
    Vis-U-All High Temp 16"x16" Self Seal Pouch 100 pouches per box; 6 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0764-2018·2018-03-07

    Steris Recalls Vis-U-All Sterilization Pouches Due to Ink Migration

    Steris Corporation is recalling Vis-U-All High Temperature Sterilization Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to medical devices.

    Product
    Vis-U-All High Temp 18"x22" Self Seal Pouch 100 pouches per box; 5 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0728-2018·2018-03-07

    Perkinelmer Recalls Janus Automated Workstations Due to Circuit Board Defect

    Perkinelmer is recalling seven Janus and Janus G3 automated workstations because defective circuit boards may cause horizontal motion errors and instrument downtime.

    Product
    JANUS & JANUS G3 Automated Workstation is an automated programmable liquid handling instrument intended for use in clinical settings to facilitate the pipetting and dilution of solutions in sample preparation work flows.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0750-2018·2018-03-07

    Steris Recalls Vis-U-All Heat Seal Pouches Due to Ink Migration

    Steris Corporation is recalling Vis-U-All High Temperature Sterilization Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to medical devices.

    Product
    Vis-U-All High Temp 10"x15" Heat Seal Pouch 100 pouches per box; 5 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0771-2018·2018-03-07

    Steris Recalls Vis-U-All High Temperature Sterilization Pouches Due to Ink Migration

    Steris is recalling Vis-U-All High Temperature Sterilization Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to medical devices.

    Product
    Vis-U-All High Temp 8"x16" Self Seal Pouch 200 pouches per box; 4 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is designed…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0755-2018·2018-03-07

    Steris Recalls Vis-U-All Heat Seal Pouches Due to Ink Migration

    Steris Corporation is recalling Vis-U-All High Temperature Sterilization Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to devices.

    Product
    Vis-U-All High Temp 3.5"x22" Heat Seal Pouch 200 pouches per box; 5 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0751-2018·2018-03-07

    Steris Recalls Vis-U-All Heat Seal Pouches Due to Ink Migration

    Steris Corporation is recalling Vis-U-All High Temp Heat Seal Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and ink transfer to devices.

    Product
    Vis-U-All High Temp 16"x16" Heat Seal Pouch 100 pouches per box; 5 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0754-2018·2018-03-07

    Steris Recalls Vis-U-All Heat Seal Pouches Due to Ink Migration

    Steris is recalling Vis-U-All High Temperature Sterilization Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to medical devices.

    Product
    Vis-U-All High Temp 4.5"x11" Heat Seal Pouch 200 pouches per box; 5 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0807-2018·2018-03-07

    Ortho Recalls VITROS Performance Verifier II Due to Stability Issues

    Ortho Clinical Diagnostics is recalling VITROS Performance Verifier II Lot K4852 because it fails long-term stability requirements for the AST analyte when refrigerated.

    Product
    VITROS Chemistry Products Performance Verifier is used as an assayed control to monitor the performance on VITROS 250/350/5, 1 FS and 4600 Chemistry Systems and the VITROS 5600 Integrated System. Used as a control for the VITROS 250/350/5,1 FS and 4600 Chemistry Systems and…
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Devices)·Z-0691-2018·2018-03-07

    CooperVision Recalls Biofinity XR Toric Contact Lenses Due to Labeling Error

    CooperVision is recalling specific Biofinity XR Toric contact lenses because the primary blister labels incorrectly identify them as Biofinity Multifocal Toric.

    Product
    Biofinity XR Toric contact lenses 8.7/14.5 - 6PK Biofinity XR Toric (comfilcon A) Soft (Hydrophilic) Contact Lenses are indicated for the correction of ametropia (myopia or hyperopia) with astigmatism) in aphakic and non-aphakic persons with non-diseased eyes in powers from…
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Devices)·Z-0753-2018·2018-03-07

    Steris Recalls Vis-U-All Heat Seal Pouches Due to Ink Migration

    Steris Corporation is recalling Vis-U-All High Temperature Sterilization Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to medical devices.

    Product
    Vis-U-All High Temp 18"x22" Heat Seal Pouch 100 pouches per box; 5 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0767-2018·2018-03-07

    Steris Recalls Vis-U-All Pouches Due to Ink Migration Defects

    Steris is recalling Vis-U-All High Temp Self Seal Pouches because purple ink may migrate onto the pouch exterior or the medical devices inside after steam processing.

    Product
    Vis-U-All High Temp 4"x11" Self Seal Pouch 200 pouches per box; 4 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is designed…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0758-2018·2018-03-07

    Steris Recalls Vis-U-All Heat Seal Pouches Due to Ink Migration

    Steris Corporation is recalling Vis-U-All High Temp Heat Seal Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to medical devices.

    Product
    Vis-U-All High Temp 7.5"x13.5" Heat Seal Pouch 200 pouches per box; 5 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0768-2018·2018-03-07

    Steris Recalls Vis-U-All High Temperature Sterilization Pouches Due to Ink Migration

    Steris Corporation is recalling Vis-U-All High Temperature Sterilization Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to enclosed devices.

    Product
    Vis-U-All High Temp 5.5"x10" Self Seal Pouch 200 pouches per box; 4 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0760-2018·2018-03-07

    Steris Recalls Vis-U-All Heat Seal Pouches Due to Ink Migration

    Steris Corporation is recalling Vis-U-All High Temperature Sterilization Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to medical devices.

    Product
    Vis-U-All High Temp 8"x16" Heat Seal Pouch 100 pouches per box; 9 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is designed…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0749-2018·2018-03-07

    Steris Recalls Vis-U-All Heat Seal Pouches Due to Ink Migration

    Steris Corporation is recalling Vis-U-All High Temp Heat Seal Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to medical devices.

    Product
    Vis-U-All High Temp 4"x8" Heat Seal Pouch 200 pouches per box; 5 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is designed…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0756-2018·2018-03-07

    Steris Recalls Vis-U-All Heat Seal Pouches Due to Ink Migration

    Steris is recalling Vis-U-All High Temp Heat Seal Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to medical devices.

    Product
    Vis-U-All High Temp 5"x15" Heat Seal Pouch 200 pouches per box; 4 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is designed…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0766-2018·2018-03-07

    Steris Recalls Vis-U-All High Temperature Sterilization Pouches Due to Ink Migration

    Steris Corporation is recalling Vis-U-All High Temperature Sterilization Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to medical devices.

    Product
    Vis-U-All High Temp 3.5"x22" Self Seal Pouch 200 pouches per box; 4 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Pouch is suitable for use by healthcare providers to enclose and seal medical devices to be sterilized by steam. The pouch is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V150000·2018-03-06

    Mercedes-Benz Recalls 2018 AMG Models for Seat Welding Defect

    Mercedes-Benz is recalling 2018 AMG C43, C63S, and E63S vehicles because improperly welded seat backrests may fail in a crash, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG C63S, AMG E63S, AMG C43
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V148000·2018-03-06

    Volkswagen Recalls Vehicles Due to Driver Air Bag Inflator Explosion Risk

    Volkswagen is recalling specific 2007-2014 models because the driver's frontal air bag inflator may explode during deployment, potentially causing serious injury or death.

    Product
    VOLKSWAGEN — VOLKSWAGEN PASSAT WAGON, GOLF, PASSAT, CC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V149000·2018-03-06

    RAM ProMaster City Recall for Steering Gear Casting Defect

    Chrysler is recalling 2018 RAM ProMaster City vehicles because a casting defect in the steering system may cause fluid leaks and increased steering effort.

    Product
    RAM — RAM PROMASTER CITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V152000·2018-03-06

    Mack Trucks Recalls 2018 Models Due to Electrical Overload Risk

    Mack Trucks is recalling 2018 Anthem, Granite, and Pinnacle trucks because an electrical overload may cause the light control module to fail, potentially disabling exterior lights and windshield wipers.

    Product
    MACK — MACK GRANITE (GU), PINNACLE (CXU), PINNACLE (PI/PN), ANTHEM (AN)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18114·2018-03-06

    Woodstream Recalls Mosquito Magnet Traps Due to Injury Hazard

    Woodstream is recalling Mosquito Magnet traps because cleaning them with Quick Clear Cartridge kits can cause the regulator to break and propel pieces, posing an injury risk.

    Product
    Mosquito Magnet traps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18116·2018-03-06

    InSinkErator Recalls SinkTop Switches for Garbage Disposals Due to Fire Hazard

    InSinkErator is recalling about 1.4 million SinkTop switches for garbage disposals because water can enter the power module, posing a fire hazard. No injuries have been reported.

    Product
    InSinkErator Single Outlet SinkTop Switches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V147000·2018-03-06

    Alfa Romeo Stelvio Recalled for Wiper Motor Software Defect

    Chrysler is recalling 2018 Alfa Romeo Stelvio vehicles because wiper motor software may limit wipers to low speed, reducing visibility and increasing crash risk.

    Product
    ALFA ROMEO — ALFA ROMEO STELVIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V153000·2018-03-06

    Nissan Recalls 2018 370Z Vehicles Due to Driver's Side Air Bag Defect

    Nissan is recalling 2018 370Z vehicles because the driver's side curtain air bag may be installed incorrectly, potentially preventing proper deployment in a crash.

    Product
    NISSAN — NISSAN 370Z
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V145000·2018-03-05

    Morgan Truck Bodies Recalled for Turn Signal Wiring Defect

    Morgan Truck Bodies LLC is recalling 2013-2018 models because water may enter the wiring harness, affecting turn signal operation and increasing crash risk.

    Product
    MORGAN — MORGAN TRUCK BODIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V146000·2018-03-05

    Triple E Recalls 2017-2018 Motorhomes Due to Incorrect Cargo Capacity Labels

    Triple E is recalling 2017-2018 Unity, Wonder, and Serenity motorhomes because incorrect labels may indicate higher cargo capacity than actual, increasing crash risk.

    Product
    TRIPLE E — TRIPLE E, TRIPLE E RV UNITY, SERENITY, WONDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·019-2018·2018-03-03

    Interstate Meat Distributors Recalls Ground Beef and Pork for E. coli Risk

    Interstate Meat Distributors is recalling approximately 14,806 pounds of ground beef and pork products due to possible E. coli O157:H7 contamination.

    Product
    Interstate Meat Dist., Inc. — Interstate Meat Distributors, Inc., Recalls Ground Beef and Pork Products due to Possible E. coli O157:H7 Contamination
    Category
    Food
    Distribution
    3 states
  • CriticalUSDA FSIS·018-2018·2018-03-02

    Olli Salumeria Americana Recalls Ready-to-Eat Meat Products Due to Listeria

    Olli Salumeria Americana is recalling approximately 3,946 pounds of ready-to-eat meat products that may be contaminated with Listeria monocytogenes.

    Product
    OLLI SALUMERIA AMERICANA — Olli Salumeria Americana Firm Recalls Ready-To-Eat Meat Products due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·017-2018·2018-03-02

    Kansas City Baking Company Recalls Ready-to-Eat Meat Products

    The Kansas City Baking Company is recalling ready-to-eat meat products produced without federal inspection and containing undeclared allergens.

    Product
    The Kansas City Baking Company Recalls Ready-To-Eat Meat Products Produced without Benefit of Inspection
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·18V143000·2018-03-02

    Keystone Recalls 2018 Recreational Trailers Due to Propane Leak Risk

    Keystone is recalling 2,958 specific 2018 recreational trailers because a loose propane valve screw may cause gas leaks and fire.

    Product
    DUTCHMEN — DUTCHMEN, KEYSTONE, CROSSROADS ASPEN TRAIL, PASSPORT, ZINGER, HIDEOUT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V144000·2018-03-02

    Newmar Recalls 2018 Essex Motorhomes Due to Taillight Detachment Risk

    Newmar is recalling 2018 Essex motorhomes because taillights may loosen and detach while driving, increasing crash risk. Dealers will secure the lights with new hardware.

    Product
    NEWMAR — NEWMAR ESSEX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·016-2018·2018-03-01

    J Bar B Foods Recalls Chicken Sausage for Undeclared Milk Allergen

    J Bar B Foods is recalling approximately 4,050 pounds of chicken sausage products because they contain milk, a known allergen, that is not declared on the label.

    Product
    J Bar B Foods — J Bar B Foods Recalls Chicken Sausage Products due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    5 states
  • SevereCPSC·18110·2018-03-01

    Double Insight Recalls Gem 65 Multicookers Due to Fire Hazard

    Double Insight is recalling Gem 65 8-in-1 multicookers sold at Walmart because a defect can cause the unit to overheat and melt, posing a fire hazard.

    Product
    Gem 65 8-in-1 multicookers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V140000·2018-03-01

    Jaguar Recalls 2018 E-Pace Vehicles Due to Front Brake Hose Bracket Defect

    Jaguar is recalling 2018 E-Pace vehicles because improperly installed front brake hose brackets may allow hoses to contact tires, causing fluid leaks and increased stopping distances.

    Product
    JAGUAR — JAGUAR E-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·015-2018·2018-03-01

    Sensenig Turkey Farm Recalls Turkey Sausage for Undeclared Allergens

    Sensenig Turkey Farm LLC is recalling approximately 1,925 pounds of raw turkey sausage products because they contain undeclared wheat and soy allergens.

    Product
    Sensenig Turkey Farm LLC — Sensenig Turkey Farm LLC Recalls Turkey Sausage Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    4 states
  • HighCPSC·18112·2018-03-01

    Graco Recalls Table2Table Highchairs Due to Rear Leg Fall Hazard

    Graco is recalling about 36,000 Table2Table 6-in-1 highchairs sold at Walmart because the rear legs can pivot out of position, creating a fall hazard.

    Product
    Graco Table2Table 6-in-1 Highchairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V142000·2018-03-01

    Coach House Recalls RVs with Defective Kidde Fire Extinguishers

    Coach House is recalling 2003-2018 recreational vehicles equipped with specific Kidde fire extinguishers that may clog or detach, posing injury risks during a fire.

    Product
    COACH HOUSE — COACH HOUSE ARRIVA, PLATINUM II, PLATINUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V141000·2018-03-01

    Ford Recalls 2017-2018 Taurus Vehicles for Ignition Key Removal Defect

    Ford is recalling 2017-2018 Taurus vehicles because the ignition key may be removed when the transmission is not in Park, increasing the risk of the vehicle rolling away.

    Product
    FORD — FORD TAURUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V139000·2018-03-01

    Land Rover Recalls 2018 Range Rover Velar for Visibility Defect

    Jaguar Land Rover is recalling 2018 Range Rover Velar vehicles because ventilation system parts may detach, preventing fog removal from windows and increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER VELAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18E011000·2018-03-01

    RockyMounts Recalls Four Bicycle Rack Models Due to Weld Failure Risk

    RockyMounts is recalling four bicycle rack models because a weld may crack, causing the rack and bicycles to separate from the vehicle and create a road hazard.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide

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