Data Foundry

Medical device recalls 2023

WATCHDOG ACCESSORY KIT — Class II medical device recall Z-1593-2023

Ongoing recall by Boston Scientific Corporation, reported 2023-05-24. The firm received complaints of the Insertion Tool component being occluded, resulting in the inability to pas

Recall numberZ-1593-2023
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmBoston Scientific Corporation, Maple Grove, MN, United States
Recall initiated2023-04-05
Classified2023-05-16
Reported by FDA2023-05-24
Quantity10,833 units
UPC / GTIN / UDI-DI08714729965770, 08714729965794
Lot numbers30319836, 30359588, 30368418, 30392647, 30409465, 30421836, 30442123, 30522919, 30564343, 30577971, 30593836, 30600837, 30600839, 30601021, 30616553, 30620297, 30625219, 30638465, 30638467, 30638469, 30638471, 30665570, 30666996, 30681966, 30681968, 30681970, 30712588, 30725194, 30780665, 30801487, 30801489, 30801491, 30811488, 30845828, 30845830, 30845832, 30885087, 30890263, 30890265, 30914070 and 6 more

Product

WATCHDOG ACCESSORY KIT (20-PACK), UPN H74939343A021 (outer package), UPN H74939343A020 (inner package)

Reason for recall

The firm received complaints of the Insertion Tool component being occluded, resulting in the inability to pass a guidewire through the tool.

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-1593-2023. 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.