Data Foundry

Medical device recalls 2026

Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only — Class II medical device recall Z-1812-2026

Ongoing recall by Wilson-Cook Medical Inc., reported 2026-04-22, distributed nationwide. Due to increased in complaints their is the potential for endoscopic clipping device to malfunction.

Recall numberZ-1812-2026
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmWilson-Cook Medical Inc., Winston Salem, NC, United States
Recall initiated2026-03-03
Classified2026-04-13
Reported by FDA2026-04-22
DistributedNationwide (US)
Countries outside the USAE, AR, AT, AU, BE, BH, BR, CA, CH, CL, CN, CO, CR, CY, CZ, DE, DK, EG, ES, FI, FR, GB, GR, GT, HK, HR, HU, ID, IE, IL, IN, KW, LB, LU, MA, MT, MX, MY, NO, NZ, OM, PE, PK, PL, PT, QA, RO, SA, SE, SI, SV, TH, TR, TW, ZA
Quantity713,702 units
Reason classesdevice malfunction
UPC / GTIN / UDI-DI10827002580104
Model numbersG58010

Product

Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO

Reason for recall

Due to increased in complaints their is the potential for endoscopic clipping device to malfunction.

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-1812-2026. 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.