Merit Medical Systems, Inc. Merit Advance Angiographic Needle label reading in part: MAJESTIK SERIES ANGIOGRAPHIC NEEDLES 20 G CATALOG NUMBER AN20T52C for the introduction of vascular access devices. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Merit Advance Angiographic Needle label reading in part: MAJESTIK SERIES ANGIOGRAPHIC NEEDLES 20 G CATALOG NUMBER AN20T52C for the introduction of vascular access devices.
Brand
Merit Medical Systems, Inc.
Lot Codes / Batch Numbers
Lot #F611693
Products Sold
Lot #F611693
Merit Medical Systems, Inc. is recalling Merit Advance Angiographic Needle label reading in part: MAJESTIK SERIES ANGIOGRAPHIC NEEDLES 20 G C due to Potential sterility breach caused by excessive shipment damage.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential sterility breach caused by excessive shipment damage.
Recommended Action
Per FDA guidance
Merit Medical Customers were contacted directly by phone and letter on 9/29/09. Customers were instructed to identify and quarantine all unused affected product. Further information was available at 801-208-4365.
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 noticeDistribution
As reported by FDA
AL, GA, KY, LA, MO, OR, TN
Page updated: Jan 10, 2026