Archive
766 recalls were announced in March 2018.
Of the 766 recalls this month scored against our rubric, 2% are Critical, 15% are Severe.
Which agencies issued them
Schmidt Baking Co. is recalling specific white wheat bread products because a vendor ingredient may contain foreign material.
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.
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.
Avid Medical is recalling 200 TruCustom DJ's Vascular/Neuro Tray kits because they may contain needles with loose polypropylene foreign material.
Philips is recalling 157 ProGrade R1 digital x-ray detectors because weak WiFi connections can cause image transfer failures, requiring patients to be re-exposed to radiation.
Schmidt Baking Co. is recalling white sandwich dinners under several brands due to a potential foreign material in an ingredient supplied by a vendor.
Bell Plantation Inc. is recalling 6,011 jars of Ready-to-Eat Powdered Peanut Butter because analytical results for non-pathogenic E. coli exceeded the firm's internal specifications.
Accord Media, LLC is recalling 1,040 units of the Ultra Renew Plus medical device because it uses an unapproved green LED light to treat hyperpigmentation.
Schmidt Baking Co. is recalling potato bread products due to a potential foreign material issue identified by a vendor. The recall affects specific Julian code dates distributed to retail centers in eight states.
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.
Meijer Distribution is voluntarily recalling select Greek and Low-fat yogurt products due to the potential risk of small glass particles.
Meijer Distribution is voluntarily recalling select Greek and Low-fat yogurt products due to a potential risk of small glass particles.
CooperVision is recalling specific Biofinity XR Toric contact lenses because the primary blister labels incorrectly identify them as Biofinity Multifocal Toric.
Perkinelmer is recalling seven Janus and Janus G3 automated workstations because defective circuit boards may cause horizontal motion errors and instrument downtime.
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.
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.
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.
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.
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.
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.
Ortho Clinical Diagnostics is recalling VITROS Performance Verifier II Lot K4852 because it fails long-term stability requirements for the AST analyte when refrigerated.
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.
Keystone Dental Inc is recalling 20 Stage-1 RDS Indexed Abutments because the expiration date on the label is incorrect.
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.
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.
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.
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.
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.
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.
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.
Ventana Medical Systems is recalling OptiView DAB IHC Detection Kits due to increased reports of leaking and sticking reagent dispensers.
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.
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.
Ventana Medical Systems is recalling iView DAB IHC Detection Kits due to increased reports of leaking and sticking reagent dispensers.
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.
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.
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.
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.
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.
Chrysler is recalling 2018 RAM ProMaster City vehicles because a casting defect in the steering system may cause fluid leaks and increased steering effort.
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.
Mercedes-Benz is recalling 2018 AMG C43, C63S, and E63S vehicles because improperly welded seat backrests may fail in a crash, increasing injury 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.
Chrysler is recalling 2018 Alfa Romeo Stelvio vehicles because wiper motor software may limit wipers to low speed, reducing visibility and increasing crash risk.
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.
Mercedes-Benz is recalling 2017 E300 and E43 AMG vehicles because misadjusted LED headlights may not illuminate the roadway properly, increasing crash risk.
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.
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.
Goodman Manufacturing is recalling about 1,650 modular blowers in the U.S. because incorrect electrical information on the serial plate could lead to fire hazards.
Morgan Truck Bodies LLC is recalling 2013-2018 models because water may enter the wiring harness, affecting turn signal operation and increasing crash risk.
Triple E is recalling 2017-2018 Unity, Wonder, and Serenity motorhomes because incorrect labels may indicate higher cargo capacity than actual, increasing crash risk.
Interstate Meat Distributors is recalling approximately 14,806 pounds of ground beef and pork products due to possible E. coli O157:H7 contamination.
Olli Salumeria Americana is recalling approximately 3,946 pounds of ready-to-eat meat products that may be contaminated with Listeria monocytogenes.
The Kansas City Baking Company is recalling ready-to-eat meat products produced without federal inspection and containing undeclared allergens.
Keystone is recalling 2,958 specific 2018 recreational trailers because a loose propane valve screw may cause gas leaks and fire.
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.
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.
Sensenig Turkey Farm LLC is recalling approximately 1,925 pounds of raw turkey sausage products because they contain undeclared wheat and soy allergens.
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.
Goodman is recalling about 534,000 packaged terminal air conditioners in the U.S. because outdoor fan motors can overheat, posing fire and burn risks.
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.
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.
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.
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.
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.
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.
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