ClearanceBrief
Recall Z-0904-05 ยท FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

Efoora, Inc. dba Virotek, L.L.C.

Virotek SAFEL*E*T 1.0 mm Safety Lancets, 1.0 mm depth, stock code 5000052, packaged in single unit blister packs, 150 or 200 per box, 6 boxes per carton; Virotek, L.L.C., 900 Asbury Dr., Buffalo Grove, IL 60089

DateJun 17, 2005 (initiated May 5, 2005)
StatusTerminated
ReasonThe sterility of the lancets may be compromised due to inadequate packaging seals.
Root causeOther
ActionEfoora/Virotek sent recall notifications to their customers via fax and DHL delivery on 5/5/05 through 5/27/05. The accounts were informed that the sterility of the lancets had been compromised due to inadequate seals. The accounts were requested to check their inventories for the affected lots, discontinue their use/distribution, and return the product to Efoora for a refund. Any questions were directed to Mary Hill, Director of Quality Assurance at 847-634-4500, ext. 277.
Quantity250,150 units
DistributionNationwide and internationally to Australia, Belgium, Bolivia, Colombia, Finland, Israel, Italy, Japan, Mexico, Nigeria, Russia, Singapore, South Africa, Spain, Sweden, Taiwan, Trinidad, United Kingdom and Zimbabwe.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.