International Technidyne Corp Tenderlett Adult Lancet, sterile, single use. Red trigger color with incision depth/length of 1.75mm/0.94mm. Manual surgical instrument for general use. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Tenderlett Adult Lancet, sterile, single use. Red trigger color with incision depth/length of 1.75mm/0.94mm. Manual surgical instrument for general use.
Brand
International Technidyne Corp
Lot Codes / Batch Numbers
Catalog No. TL100A and TL100I: NL512, NL513, NL514, NL515, NL516, NL517, NL518, NL520, NL524, NL525, NL526, NL527, NN521, NP501, NP502, NP503, NP504.
Products Sold
Catalog No. TL100A and TL100I: NL512; NL513; NL514; NL515; NL516; NL517; NL518; NL520; NL524; NL525; NL526; NL527; NN521; NP501; NP502; NP503; NP504.
International Technidyne Corp is recalling Tenderlett Adult Lancet, sterile, single use. Red trigger color with incision depth/length of 1.75m due to Some packages contained a pin-hole defect that permitted the transmission of dye through the primary packaging. This is a sterile product.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Some packages contained a pin-hole defect that permitted the transmission of dye through the primary packaging. This is a sterile product.
Recommended Action
Per FDA guidance
Recall letter was sent out 1/25/2006 via UPS tracking system per the distribution record addressees. With Cardinal Health, the letter was sent out to the firm''s corporate headquarters location.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026