FDA recall Z-0772-2023

TELEFLEX LLC · Class II · device

Product

Pilling Wecksorb Cylindrical Sponges

Reason for recall

Specific lots have not been irradiated to eliminate pyronema and therefore the sterility of the affected products may be compromised.

Distribution

Domestic distribution to IL, MS, PA, TN.

Key facts

Status
Ongoing
Initiation date
2022-09-28
Report date
2023-01-04
Voluntary/Mandated
Voluntary: Firm initiated
Location
Morrisville, NC, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0772-2023