Recalls for 01/28/2020

Clozaril, Fazaclo ODT, Versacloz (clozapine): Drug Safety Communication - FDA Strengthens Warning That Untreated Constipation Can Lead to Serious Bowel Problems
01/28/2020 Medical Recall

FDA is strengthening an existing warning that constipation caused by the schizophrenia medicine clozapine (Clozaril, Fazaclo ODT, Versacloz, generics) can, uncommonly, progress to serious bowel complications. This can lead to hospitalization or even death if constipation is not diagnosed/treated.

2018 LION LION C - SERVICE BRAKES, HYDRAULIC:POWER ASSIST:HYDRAULIC:HOSES, LINES/PIPING, AND FITTINGS
01/28/2020 Vehicle Recall

Lion Electric Company (Lion) is recalling certain 2018-2020 Lion C electric school buses. During a sudden braking and change of direction combination, a decrease in the hydraulic system pressure can occur, causing a loss of power steering and power braking.

  • Company:
    LION
  • Recall Number
    20V028000
2019 ARCIMOTO FUV - SERVICE BRAKES | STEERING:LINKAGES
01/28/2020 Vehicle Recall

Arcimoto Inc. (Arcimoto) is recalling certain 2019 FUV motorcycles. During full right steering lock, the brake line may contact the steering main-link.

  • Company:
    ARCIMOTO
  • Recall Number
    20V032000
Salud Natural Entrepreneur Inc. Recalls Nopalina Flax Seed Fiber Powder and Nopalina Flax Seed Fiber Capsules Because of Possible Health Risk
01/28/2020 Food Recall

Salud Natural Entrepreneur, Inc. of Waukegan, IL is voluntarily recalling Nopalina Flax Seed Fiber (powder) and Nopalina Flax Seed Fiber (capsule) products due to possible Salmonella contamination

Distributor Teleflex Recalls the Galemed Babi.Plus Pressure Relief Manifolds Due to Dislodged Valve
01/28/2020 Medical Recall

The Babi.Plus Pressure Relief Manifold is used as part of a breathing circuit to assist infant patients to breathe. This device is being recalled due to a dislodged valve resulting in loss of pressure in the system. Teleflex issued a Medical Device Recall Notice to affected customers.