Stealth Spring Clip (Applied Medical) – occlusion failure (2020)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
STEALTH SPRING CLIP 6mm latis (1/2 Force). REF/UDI::A1601/(01)00607915110567 - Product Usage: The device is indicated for surgical clamping during cardiovascular, peripheral vascular, and general surgery.
Brand
Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa
Lot Codes / Batch Numbers
LOT # 1359929, Manufacture Date June 28, 2019, Expiration Date June 26, 2024
Products Sold
LOT # 1359929, Manufacture Date June 28, 2019; Expiration Date June 26, 2024
Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa is recalling STEALTH SPRING CLIP 6mm latis (1/2 Force). REF/UDI::A1601/(01)00607915110567 - Product Usage: The de due to Failure of cardiovascular clips to provide sufficient occlusion of the vessel.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
Recommended Action
Per FDA guidance
On 01/31/2020, Customer Notification Letter was sent to all consignees/ distributors requesting them to return the affected devices to the recalling firm.
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