Boston Scientific Corp ''NAMIC Custom Angiographic Kit'' sold under the following labels: (1) Medical University of South Carolina. Pouch Catalog # 60131481; (2) Covenant Medical Center, Pouch Catalog #60131603; (3) St. Joseph Hospital, Pouch Catalog #60101041; (4) Spectrum Health, Pouch Catalog #61020031 (5) Rush Foundation Hospital, Kit #65185472 ****** Responsible firm on product labels: Boston Scientific/SCIMED *** Manufactured by: Boston Scientific Corporation / NAMIC Technology Center / Glens Falls, New Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
''NAMIC Custom Angiographic Kit'' sold under the following labels: (1) Medical University of South Carolina. Pouch Catalog # 60131481; (2) Covenant Medical Center, Pouch Catalog #60131603; (3) St. Joseph Hospital, Pouch Catalog #60101041; (4) Spectrum Health, Pouch Catalog #61020031 (5) Rush Foundation Hospital, Kit #65185472 ****** Responsible firm on product labels: Boston Scientific/SCIMED *** Manufactured by: Boston Scientific Corporation / NAMIC Technology Center / Glens Falls, New
Brand
Boston Scientific Corp
Lot Codes / Batch Numbers
(1) Medical University of SC label: Lot 942414 (2) Covenant label: Lot 939982, 943645, (3) St. Joseph label: Lot 940424, (4) Spectrum label: Lot 940054 (5) Rush Foundation label: Lot 945456, 943043
Products Sold
(1) Medical University of SC label: Lot 942414 (2) Covenant label: Lot 939982, 943645; (3) St. Joseph label: Lot 940424; (4) Spectrum label: Lot 940054 (5) Rush Foundation label: Lot 945456; 943043
Boston Scientific Corp is recalling ''NAMIC Custom Angiographic Kit'' sold under the following labels: (1) Medical University of Sout due to Molded handles used in Angiographic Manifolds may be occluded.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Molded handles used in Angiographic Manifolds may be occluded.
Recommended Action
Per FDA guidance
Letters dated 5/4/2004 to Risk Managers with instructions to return product.
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
IL, IN, KY, MI, SC, TX
Page updated: Jan 10, 2026