FDA recall Z-1505-2020

TeDan Surgical Innovations LLC · Class II · device

Product

DS-0022 QUICK START DISTRACTION SCREW 12MM 5/BOX STERILE - Product Usage: These products are intended to be used by trained surgeons and are designed for use with TSI distractors and screwdrivers.

Reason for recall

The items identified for recall are labeled as sterile. However, the manufacturer has found that product packaging for the lots listed above may be damaged, potentially exposing the product to non sterile conditions. This situation presents a risk of infection to patients.

Distribution

Worldwide.

Key facts

Status
Terminated
Initiation date
2019-02-18
Report date
2020-03-25
Termination date
2021-01-12
Voluntary/Mandated
Voluntary: Firm initiated
Location
Sugar Land, TX, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1505-2020