FDA recall Z-1683-2022

Product

Medline CHEST TUBE REORDER NO: DYNJ36762A

Reason for recall

Due to a non-sterile component (tape) being place within the sterile portion of the Chest Tube Convenience Kit

Distribution

U.S. Nationwide distribution in the state of AL.

Key facts

Status

Ongoing

Initiation date

2022-07-21

Report date

2022-09-14

Voluntary/Mandated

Voluntary: Firm initiated

Location

Laredo, TX, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1683-2022