ClearanceBrief
Recall Z-1118-2022 ยท EFQ Gauze/Sponge, Internal

Steris Corporation

Ultra Pure Non-Woven Sponges Non-Sterile 4-Ply 5,000 per case 25 sleeves of 200 2 in x 2 in / 5.1 cm x 5.1 cm Model Number: ENC100

DateMar 22, 2022
StatusTerminated
ReasonProduct not approved for release for US distribution
Root causeOther
ActionCrosstex notified accounts by Urgent Medical Device Recall letter dated 3/22/22 via email. Letter states reason for recall, health risk and action to take: 1. Please immediately inspect on-hand inventory for Ultra Pure Non-Woven Sponges, lot #202108 (part numbers ENC100 and ENC4100). 2. Please reply via email or complete the Recall Response Form included with this Notification Letter and return to cvalderrama@hu-friedy.com. Crosstex will provide instructions for returning the affected product to us. 3. Identify and notify all Customers who you have further distributed the affected product. Imp
Quantity103 cases
DistributionNationwide
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K984187CROSSTEX NON-WOVEN SPONGES
Crosstex Intl., Feb 18, 1999