FDA recall Z-0803-2022

CellEra LLC · Class III · device

Product

20544 Vitale Silver calcium Alginate Dressings 4x4, 10/box

Reason for recall

Firm discovered that an incorrect version of the Instructions for Use (IFU) containing language beyond the cleared 510(k) were inserted in the affected products. Firm is replacing these with the correct version of the IFU.

Distribution

US Nationwide distribution.

Key facts

Status
Terminated
Initiation date
2021-12-15
Report date
2022-03-23
Termination date
2023-10-16
Voluntary/Mandated
Voluntary: Firm initiated
Location
Monroe, OH, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0803-2022