Data Foundry

Medical device recalls 2024

Capio SLIM Suture Capturing Device — Class II medical device recall Z-2452-2024

Ongoing recall by Boston Scientific Corporation, reported 2024-08-07, distributed nationwide. Some lots of Capio SLIM do not consistently catch the suture after activation possibly resulting in a prolonge

Recall numberZ-2452-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmBoston Scientific Corporation, Marlborough, MA, United States
Recall initiated2024-06-27
Classified2024-07-30
Reported by FDA2024-08-07
DistributedNationwide (US)
Quantity70,890 units
UPC / GTIN / UDI-DI08714729838005
Lot numbers29729168, 29729169, 29972338, 30110291, 30110294, 30254836, 30254837, 30331858, 30338212, 30362314, 30367934, 30434163, 30437947, 30551935, 30598976, 30842709, 30860944, 30993213, 30997334, 31005909, 31257604, 31292169, 31352417, 31367044, 31535491, 31544821, 31554784, 31574100, 31574101, 31624545, 31638194, 31648501, 31727288, 31755722, 31856165, 31856166, 31876917, 31876918, 31876919, 31942747 and 21 more

Product

Capio SLIM Suture Capturing Device, 1-Pack, UPN: M0068318250. Capio SLIM Suture Capturing Devices are used by physicians to facilitate the consistent placement of sutures during open surgical procedures.

Reason for recall

Some lots of Capio SLIM do not consistently catch the suture after activation possibly resulting in a prolonged procedure or additional medical intervention.

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-2452-2024. 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.