Data Foundry

Medical device recalls 2026

Boston Scientific ENROUTE Transcarotid Neuroprotection System Plus — Class I medical device recall Z-2978-2026

Ongoing recall by Boston Scientific Corporation, reported 2026-08-26, distributed nationwide. Potential for arterial sheath tip separation or partial tip separation during use.

Recall numberZ-2978-2026
Product typeMedical device
ClassificationClass I
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmBoston Scientific Corporation, Maple Grove, MN, United States
Recall initiated2026-07-09
Classified2026-08-20
Reported by FDA2026-08-26
DistributedNationwide (US)
Countries outside the USAU, CA, CN, JM
Quantity49,229 units
UPC / GTIN / UDI-DI00811311021062
Lot numbers305736-2, 305737, 305738, 305913, 305929, 305940, 306079, 306085, 306093, 306097, 306115, 306168, 306178, 306187, 306195, 306200, 306207, 306219, 306232, 306242, 306244, 306272, 306279, 306290, 306305, 306311, 306319, 306320, 306328, 306338, 306348, 306359, 306372, 306391, 306408, 306420, 306431, 306440, 306453, 306460 and 77 more

Product

Boston Scientific ENROUTE Transcarotid Neuroprotection System Plus, Material Number SR-250-NPS; Percutaneous catheter

Reason for recall

Potential for arterial sheath tip separation or partial tip separation during use.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2978-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.