FDA recall Z-0194-2020

TIDI PRODUCTS · Class II · device

Product

Posey Connected Twice-As-Tough Cuffs

Reason for recall

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

Key facts

Status
Terminated
Initiation date
2019-04-12
Report date
2019-11-06
Termination date
2020-07-22
Voluntary/Mandated
Voluntary: Firm initiated
Location
Lake Forest, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0194-2020