Lake Forest, IL, United States
TIDI PRODUCTS recalls
1 recall recorded since 2018, most recently on 12 April 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
- 12 April 2019
- Terminated
- 22 July 2020
- Reason
- Not meeting design specifications.
- Distribution
- AK, AR, CA, CT, FL, GA, IA, IL, IN, KS, LA, MA, MD, ME, MN, MO, MS, MT, NC, NH, NJ, NM, NY, PA, SC, TN, TX, UT, VA, VT, WI, and WV CANADA, FRANCE, and THE NETHERLANDS
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0194-2020
- Posey Connected Twice-As-Tough Cuffs
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.