# FDA recall Z-0194-2020

> **TIDI PRODUCTS** · Class II · device recall initiated 2019-04-12.

## 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

- **Recall number:** Z-0194-2020
- **Recalling firm:** TIDI PRODUCTS
- **Classification:** Class II
- **Product type:** device
- **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

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

## Citation

> AI Analytics. FDA recall Z-0194-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0194-2020. Source: US FDA. Licensed CC0.

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