Recall Z-0194-2020— TIDI PRODUCTS
Class II · Terminated
Class II FDA medical device recall by TIDI PRODUCTS, initiated 2019-04-12, terminated 2020-07-22. FDA's recall record names no specific 510(k) clearance for this event. Product: Posey Connected Twice-As-Tough Cuffs. Reason: Not meeting design specifications..
- Recalling firm
- TIDI PRODUCTS
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2019-04-12
- Terminated
- 2020-07-22
- Firm location
- Lake Forest, IL, United States
Product description
Posey Connected Twice-As-Tough Cuffs
Reason for recall
Not meeting design specifications.
Data sourced from openFDA. This site is unofficial and independent of the FDA.