Recall StatusTerminated
Date Initiated2019-04-12
Date Terminated2020-07-22
Product Quantity7692 (7615 USA and 77 OUS)
Reason for Recall
Not meeting design specifications.
Firm Action
On April 5th the firm sent letters to their customers stating the following: Next Steps:
1. Ensure that all caregivers and users of the Posey Connected Twice-As-Tough (TAT) Cuffs (nos. 2796 and 2797) are made aware of this Recall Notice.
2. Refer to the enclosed TAT Cuff Lot Number List (Attachment 1) and check your inventory to determine if your facility has any affected units.
3. Destroy affected TAT Cuff(s) by following the enclosed TAT Cuff Destruction Instructions (Attachment 2). Dispose of damaged products per your facilitys policy for BIOHAZARDOUS material.
4. Complete the enclosed Customer Response and Proof of Destruction Form and return this form to the TIDI Products Regulatory Department.
5. Product Replacement Product shipment will resume on or around April 12, 2019. Replacement orders will be fulfilled as Customer Response and Proof of Destruction Forms are received. Note: If you have zero inventory of affected product, please enter 0 in the Quantity section and return form as required.
Distribution of this Recall Notice:
Please distribute this Recall Notice to appropriate individuals within your organization and to any organization where the potentially affected devices were transferred or sold.
Please maintain awareness of this notice and resulting action for a minimum of two years to ensure
effectiveness of this corrective action.
In cases where customers opt not to proceed with completion of the recall requirements described
above, TIDI Products cannot accept any responsibility for safety related issues or legal liabilities
caused by the failure to respond to this Recall Notice.
We regret any inconvenience that this Recall Notice may cause.
Note: Adverse reactions or quality problems experienced with the use of this product may be
reported to the FDAs MedWatch Adverse Event Reporting program either online, by regular mail or
by fax.
Additional Comment
If you have any further questions or require assistance completing the Cust
Root Cause
Process control
Distribution Pattern
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
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.