Redondo Beach, CA, United States
Quantimetrix Corporation recalls
1 recall recorded since 2018, most recently on 21 December 2017. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class III Medical devices
- Recall started
- 21 December 2017
- Terminated
- 27 January 2021
- Reason
- The kits contained an incorrect lot of Dropper Plus Level 1 vials
- Distribution
- US Distribution to the state of : Kansas
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2257-2018
- Dropper Plus Point-of-Care Urinalysis Dipstick Control kit The Quantimetrix Dropper Plus Point-of-Care Urinalysis Dipstick Control is intended as a control for urinalysis reagent strips, microalbumin, and creatinine b
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.