Boston Scientific Corporation: Medical Device Recall in 2024 - (Recall #: Z-1517-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

EndoVive 20 Fr Safety PEG Push w/ENFit Kit (Box 2)-Indicated for enteral nutrition directly into the stomach in both pediatric and adult patients who are unable to consume nutrition by conventional means. UPN: M00509191

Product Classification:

Class II

Date Initiated: February 20, 2024

Date Posted: April 17, 2024

Recall Number: Z-1517-2024

Event ID: 94165

Reason for Recall:

Inability to advance the guidewire through the feeding tube during placement due to blocked lumen of the barb connector. May lead prolongation in the procedure to exchange the device for another leading to leading to a cascade of events which may include additional intervention to close the puncture site, bleeding, leakage of gastric contents, and aspiration

Status: Ongoing

Product Quantity: 13 units (Japan)

Code Information:

GTIN: 08714729880691 Lot Numbers: 32234291

Distribution Pattern:

Worldwide distribution - US Nationwide and the country of Japan.

Voluntary or Mandated:

Voluntary: Firm initiated