EndoVive Safety PEG Kit; Outer Box Material Number (UPN): M00509001; Inner Box Material Number (UPN): M00509000;
FDA Recall Z-1551-2026 · Posted 2026-03-11
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Recalling FirmBoston Scientific Corporation
Recall StatusOpen, Classified
Product CodePIF
Date Initiated2026-02-10
Product Quantity806 units
Reason for Recall
Recall of kits which utilized ChloraPrep Triple Swabsticks from BD. Open or compromised seals on the sterile swabstick packaging, which could result in loss of sterility or drying of the antiseptic solution. This component is placed outside of the sterile barrier of the tray manufactured by Boston Scientific, which contains the majority of the kit
components. As such, inclusion of the affected ChloraPrep Triple Swabsticks does not degrade the integrity of the other components within the PEG kit.
Firm Action
On February 10, 2026 Urgent Medical Device Removal - Immediate Action Required letters were sent to customers.
Actions to be taken:
" Do NOT use affected product (Attachment 1), remove affected product from your facility s
inventory, and segregate the units in a secure place until they can be returned to Boston
Scientific.
" Immediately post this information in a visible location near the affected products to ensure this
information is readily accessible to all handlers and users of the device.
" Forward this notice to any healthcare professional from your organization for awareness and to
any organization where affected devices have been transferred.
" Complete and return the enclosed Reply Verification Tracking Form per the enclosed
instructions.
" Return affected product.
This removal affects only the products and lots affected. No other
material numbers or lots are impacted by this removal. If you are a facility that has sent products to another hospital or a facility within your network, ensure this notification is forwarded to them.
Root Cause
Process control
Distribution Pattern
US Nationwide distribution.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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