M.D.L. S.r.l. Via Tavani N. 1/A Delebio Italy Aspirated Cyto-Histological Biopsy needle Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Aspirated Cyto-Histological Biopsy needle
Brand
M.D.L. S.r.l. Via Tavani N. 1/A Delebio Italy
Lot Codes / Batch Numbers
Model PB1810, Lot 1617A Model PB1815, Lots 5216C and 3620D Model PB1820, Lot 5216C Model PB1825, Lot 5216C Model PB2010, Lot 1617A Model PB2015, Lots 5216C, 2618B, and 3620D Model PB2020, Lots 5216C and 1618A Model PB2110, Lot 5216C Model PB2115, Lot 5216C Model PB2120, Lot 1617A Model PB2215, Lot 5216C Model PB2220, Lots 5216C, 1618A, 3620D Model PB2225, Lot 2518A
Products Sold
Model PB1810; Lot 1617A Model PB1815; Lots 5216C and 3620D Model PB1820; Lot 5216C Model PB1825; Lot 5216C Model PB2010; Lot 1617A Model PB2015; Lots 5216C, 2618B, and 3620D Model PB2020; Lots 5216C and 1618A Model PB2110; Lot 5216C Model PB2115; Lot 5216C Model PB2120; Lot 1617A Model PB2215; Lot 5216C Model PB2220; Lots 5216C, 1618A, 3620D Model PB2225; Lot 2518A
M.D.L. S.r.l. Via Tavani N. 1/A Delebio Italy is recalling Aspirated Cyto-Histological Biopsy needle due to Sterility assurance may be compromised.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Sterility assurance may be compromised.
Recommended Action
Per FDA guidance
The firm disseminated an URGENT: MEDICAL DEVICE RECALL notice on 08/05/2021 by email. The notice explained the issue and requested the return of any unused products. Distributors were instructed to notify their customers.
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