FDA recall Z-2000-2019

Terumo Medical Corporation · Class II · device

Product

Terumo Sur-vet Needle, 22G x 3/4", Product Code 100215

Reason for recall

There is a potential for a loss of package integrity that may compromise the sterility of the product.

Distribution

The products were distributed to the following US states: FL, IN, KS, KY, MA, MO, NH, NV, PA, SC, TN, and TX.

Key facts

Status
Terminated
Initiation date
2019-02-08
Report date
2019-07-31
Termination date
2020-05-08
Voluntary/Mandated
Voluntary: Firm initiated
Location
Elkton, MD, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2000-2019