Pleasanton, CA, United States
PROVIDENCE MEDICAL TECHNOLOGIES recalls
1 recall recorded since 2018, most recently on 29 March 2019. 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 II Medical devices
- Recall started
- 29 March 2019
- Terminated
- 27 May 2022
- Reason
- There may be dimensional manufacturing error that represents a potential safety risk to patients.
- Distribution
- US Nationwide distribution including in the states of AZ, CA, FL, IL, IN, LA, MA, MO, NC, NJ, NY, OH, OR and TX.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2428-2020
- Ally Bone Screw - Product Usage:Bone Screws are indicated for use in bone reconstruction, osteotomy, arthrodesis, joint fusion, fracture repair, and fracture fixation appropriate for the size of the device. Screws are in
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.