Recalls for 04/14/2020

2020 CHEVROLET 6500XD - ELECTRICAL SYSTEM:WIRING
04/14/2020 Vehicle Recall

Isuzu Technical Center of America, Inc. (Isuzu) is recalling certain 2018-2020 FTR and Chevrolet 6500XD vehicles. The chassis wire harness outside the relay box may have been improperly routed, potentially allowing the harness to contact the suspension's leaf spring hanger bracket, allowing the harness to get chafed.

  • Company:
    CHEVROLET
  • Recall Number
    20V195000
2020 CHEVROLET 6500XD - ELECTRICAL SYSTEM:WIRING
04/14/2020 Vehicle Recall

Isuzu Technical Center of America, Inc. (Isuzu) is recalling certain 2018-2020 FTR and Chevrolet 6500XD vehicles. The chassis wire harness outside the relay box may have been improperly routed, potentially allowing the harness to contact the suspension's leaf spring hanger bracket, allowing the harness to get chafed.

  • Company:
    ISUZU
  • Recall Number
    20V195000
2020 TRANS TECH ROADSTAR - ELECTRICAL SYSTEM: INSTRUMENT PANEL | SEAT BELTS:FRONT:WARNING LIGHT/DEVICES
04/14/2020 Vehicle Recall

Trans Tech Bus (Trans Tech) is recalling certain 2020 Roadstar, ST Aero and SST buses built on 2019 Chevrolet Express cutaway chassis. The specific models are AC139SSSA409,AC139SSSP500, CC139DMSA409, CC139DMSA500, CC139DMSP500, CC159DMSA509, CC159DMSA600,EC139DBSP400, SC139DSFP500, SC139DSSA409, SC139DSSA500, SC139DSSP500, SC159DSFP600, SC159DSSA509, SC159DSSA600, SC159DSSA603, SC159DSSP600, and SC177DSSA603. The seatbelt-unfastened warning light will not illuminate for approximately five seconds after the ignition is moved to the "on" or "start" position. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 208, "Occupant Crash Protection."

  • Company:
    TRANS TECH
  • Recall Number
    20V196000
2020 KENWORTH T170 - ELECTRONIC STABILITY CONTROL | SERVICE BRAKES, AIR:ANTILOCK:ABS WARNING LIGHT
04/14/2020 Vehicle Recall

PACCAR Incorporated (PACCAR) is recalling certain 2008-2019 Peterbilt 330, 335, 337, 340, 348, 365, 367, 384, 386, 387, 388, 389, 567, 579 and 587 vehicles and 2008-2020 Kenworth T170, T270, T370, T660, T680, T800, T880, and W900 vehicles equipped with NAMUX Software. In the event that the Anti-lock Brake System (ABS) loses battery and/or ignition power to the controller, the dash warning light for the ABS may not illuminate to warn the driver of the loss of ABS. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 121, "Air Brake Systems," and 136, "Electronic Stability Control System on Heavy Vehicles."

  • Company:
    PETERBILT
  • Recall Number
    20V199000
Baxter Expands Voluntary Nationwide Recall to Include Second Lot of Nexterone Injection Due to Presence of Particulate Matter
04/14/2020 Medical Recall

Following the issuance of a voluntary recall dated November 10, 2017 of one lot of NEXTERONE (amiodarone HCl) 150 mg/100 mL Premixed Injection, Baxter International Inc. announced today it is expanding the recall to include a second lot (NC109123) of NEXTERONE due to the potential presence of particulate matter.

2020 KENWORTH T170 - ELECTRONIC STABILITY CONTROL | SERVICE BRAKES, AIR:ANTILOCK:ABS WARNING LIGHT
04/14/2020 Vehicle Recall

PACCAR Incorporated (PACCAR) is recalling certain 2008-2019 Peterbilt 330, 335, 337, 340, 348, 365, 367, 384, 386, 387, 388, 389, 567, 579 and 587 vehicles and 2008-2020 Kenworth T170, T270, T370, T660, T680, T800, T880, and W900 vehicles equipped with NAMUX Software. In the event that the Anti-lock Brake System (ABS) loses battery and/or ignition power to the controller, the dash warning light for the ABS may not illuminate to warn the driver of the loss of ABS. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 121, "Air Brake Systems," and 136, "Electronic Stability Control System on Heavy Vehicles."

  • Company:
    KENWORTH
  • Recall Number
    20V199000
2020 KTM 790 ADVENTURE - SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:HOSES, LINES/PIPING, AND FITTINGS
04/14/2020 Vehicle Recall

KTM North America, Inc. (KTM) is recalling certain 2019-2020 790 Adventure and 790 Adventure R motorcycles. The rear brake hose may overheat, causing the rear brake system to fail.

  • Company:
    KTM
  • Recall Number
    20V198000
2020 FORD EXPEDITION - POWER TRAIN:AUTOMATIC TRANSMISSION:GEAR POSITION INDICATION (PRNDL)
04/14/2020 Vehicle Recall

Ford Motor Company (Ford) is recalling certain 2020 Ranger and F-150 vehicles equipped with 10-speed automatic transmissions and certain 2020 Expedition vehicles equipped with a "police" package. The transmission shift cable lock clip may not be fully seated, allowing the transmission to actually be in a different gear than the gear shift position selected by the driver.

  • Company:
    FORD
  • Recall Number
    20V197000
2020 TOYOTA COROLLA HATCHBACK - EXTERIOR LIGHTING:BACK UP LIGHTS
04/14/2020 Vehicle Recall

Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2020 Corolla Hatchback vehicles. A rear hatch wire harness connector may have been damaged during assembly, which may cause the back-up lights to fail.

  • Company:
    TOYOTA
  • Recall Number
    20V205000
2020 JEEP COMPASS - VISIBILITY:WINDSHIELD WIPER/WASHER:LINKAGES
04/14/2020 Vehicle Recall

Chrysler (FCA US LLC) is recalling certain 2019-2020 Ram 1500, 1500 Classic and Jeep Compass vehicles. The windshield wiper arm or arms may loosen, possibly causing the wipers to not operate properly and reduce the driver's visibility in certain weather conditions.

  • Company:
    RAM
  • Recall Number
    20V208000
2020 JEEP COMPASS - VISIBILITY:WINDSHIELD WIPER/WASHER:LINKAGES
04/14/2020 Vehicle Recall

Chrysler (FCA US LLC) is recalling certain 2019-2020 Ram 1500, 1500 Classic and Jeep Compass vehicles. The windshield wiper arm or arms may loosen, possibly causing the wipers to not operate properly and reduce the driver's visibility in certain weather conditions.

  • Company:
    JEEP
  • Recall Number
    20V208000
Pharmedium Services, LLC Expands Voluntary Nationwide Recall of Additional Lots of Compounded Sterile Products Within Expiry Due to Lack of Sterility Assurance
04/14/2020 Medical Recall

January 10, 2018 Lake Forest, IL PharMEDium Services, LLC (PharMEDium) is voluntarily expanding the recall issued on December 27, 2017 to include the below lots of sterile drug products to the hospital/user level due to a lack of assurance of sterility. Administration of a drug product intended to be sterile that is not sterile could result in serious infections that may be life-threatening.

PharMEDium Services, LLC Issues Voluntary Nationwide Recall of Certain Lots of Compounded Sterile Products Due to Lack of Sterility Assurance
04/14/2020 Medical Recall

December 27, 2017 Lake Forest, IL PharMEDium Services, LLC (PharMEDium) is voluntarily recalling the below lots of drug products to the hospital/user level due to a lack of assurance of sterility. Administration of a drug product intended to be sterile that is not sterile could result in serious infections that may be life-threatening. To date, PharMEDium has not received any reports of complaints related to the products but is issuing this recall out of an abundance of caution following a commitment made during a recent inspection of the company’s facility.

2019 TEREX DIGGER DERRICK - ELECTRICAL SYSTEM:STARTER ASSEMBLY | ENGINE
04/14/2020 Vehicle Recall

Terex South Dakota, Inc. (Terex) is recalling certain 2018-2019 C4045, C4047, C5050, and C7066 Digger Derrick vehicles. Due to an engine computer program error, if the hood switch fails or opens, the remote engine start/stop function becomes disabled.

  • Company:
    TEREX
  • Recall Number
    20V200000
AuroMedics Pharma LLC Issues Voluntary Nationwide Recall of Levofloxacin in 5% Dextrose 250mg/50mL Due to Presence of Visible Particulate Matter Tentatively Identified as Mold
04/14/2020 Medical Recall

FOR IMMEDIATE RELEASE – 01-12-2018 – East Windsor, New Jersey, AuroMedics Pharma LLC is voluntarily recalling one lot of Levofloxacin in 5% Dextrose Injection 250mg/50mL in a Single-Use flexible container NDC 55150-243-46, Lot CLF160003, Expiry date May 2018, to the hospital level. The product has been found to contain visible particulate matter tentatively identified as mold. This problem was discovered as a result of a product complaint in which the contents of one flexible bag was found to contain white particulate matter

2020 VAC-TRON MC 533 SDT - EXTERIOR LIGHTING
04/14/2020 Vehicle Recall

Vac-Tron Equipment, LLC. (Vac-Tron) is recalling certain 2012-2020 MC555SDT, MC533SDT and MC573SDT Vacuum Excavator trailers. The trailer's front clearance lamps are positioned improperly, the jetter blocks visibility to the passenger side front clearance lamp, and an insufficient amount of conspicuity tape may have been applied on the sides and rear. The trailers may also may also lack side or rear reflex reflectors. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 108, "Lamps, Reflective Devices, and Associated Equipment."

  • Company:
    VAC-TRON
  • Recall Number
    20V201000
2021 GREAT DANE EVEREST - WHEELS:LUGS/NUTS/BOLTS
04/14/2020 Vehicle Recall

Great Dane Trailers (Great Dane) is recalling certain 2020-2021 Everest Refrigerated Vans. The axle nut retaining clips may have been improperly installed, potentially resulting in loose wheels and loss of vehicle control.

  • Company:
    GREAT DANE
  • Recall Number
    20V202000
2020 SPARTAN GLADIATOR - PARKING BRAKE
04/14/2020 Vehicle Recall

Marion Body Works Inc. (Marion Body Works) is recalling certain 2019-2020 Spartan Gladiator and MetroStar Emergency Response chassis vehicles modified by Marion Body Works. The park brake control line may loosen and possibly come out the fitting while the vehicle is in motion.

  • Company:
    SPARTAN
  • Recall Number
    20V203000
Use Caution with Implanted Pumps for Intrathecal Administration of Medicines for Pain Management: FDA Safety Communication
04/14/2020 Medical Recall

The FDA is providing recommendations and sharing important information with health care providers, pharmacists, compounders, patients and caregivers about the risks of using medications delivered into the spinal fluid to treat or manage pain that are not approved for use with the implanted pumps.