FDA recall Z-0016-2019

COVIDIEN LLC · Class II · device

Product

Kerlix Bandage Roll, 100 Cotton, 8 Ply, Large 4-1/2 x 9.3 (11.4 cm x 2.8 m), REF 6716 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.

Reason for recall

Potential for product sterility breach due to a compromised or pinched seal defect

Distribution

US Nationwide Distribution

Key facts

Status
Terminated
Initiation date
2018-08-01
Report date
2018-10-10
Termination date
2020-06-03
Voluntary/Mandated
Voluntary: Firm initiated
Location
Mansfield, MA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0016-2019