Class II — TIDI PRODUCTS
| Recalling firm | TIDI PRODUCTS, LLC |
|---|---|
| Registered facility | View this company's 4 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Not meeting design specifications. |
| Product | Posey Connected Twice-As-Tough Cuffs |
| Quantity | 7692 (7615 USA and 77 OUS) |
| 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 | 2019-04-12 |
| Classified | 2019-10-25 |
| Terminated | 2020-07-22 |
| Recall number | Z-0194-2020 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — TIDI PRODUCTS (Z-0194-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/82534/
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