WhichRecall
Class IIReported 2026-03-18

EndoVive Safety PEG Kit; Outer Box Material Number (UPN): M00509001; Inner Box Material Number (UPN): M00509000;

Recalled by Boston Scientific Corporation

Reason for Recall

Recall of kits which utilized ChloraPrep Triple Swabsticks from BD

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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.

Recall Number
Z-1551-2026
Classification
Class II
Status
Ongoing
Category
device
Initiated
2026-02-10
Reported
2026-03-18
Distribution
US Nationwide distribution.
Code Info
Outer Box Material Number (UPN): M00509001; Inner Box Material Number (UPN): M00509000; Outer Box UDI: 08714729880394; Inner Box UDI: 08714729880387; Outer Box Lot#s: 37435463, 37522541, 37528545, 37546847, 37546850, 37546849, 37550500, 37592036, 37732292; Inner Box Lot#s: 37435462, 37514809, 37525231, 37536563, 37536564, 37536562, 37546840, 37583642, 37731897;
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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