ClearanceBrief
Recall Z-1998-2019 ยท FMI Needle, Hypodermic, Single Lumen

Terumo Medical Corporation

Terumo Sur-vet Needle, 20G x 1", Product Code 100204

DateFeb 8, 2019
StatusTerminated
ReasonThere is a potential for a loss of package integrity that may compromise the sterility of the product.
Root causePackaging
ActionUrgent Voluntary Medical Device Recall notification letters dated 2/8/19 were sent to customers.
Quantity729,000
DistributionThe products were distributed to the following US states: FL, IN, KS, KY, MA, MO, NH, NV, PA, SC, TN, and TX.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K121607TERUMO(R) NEEDLE
Terumo (Philippines) Corporation, Nov 8, 2012