Data Foundry

Medical device recalls 2021

Gore Propaten Vascular Graft configured for Pediatric Shunt — Class II medical device recall Z-2293-2021

Ongoing recall by W L Gore & Associates, Inc., reported 2021-08-25, distributed in AZ, CA, DC, GA, IL, KY, MA, MD…. Vascular Grafts containing an inner diameter of 6 mm may be incorrectly labeled as 5 mm and Vascular Grafts co

Recall numberZ-2293-2021
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmW L Gore & Associates, Inc., Flagstaff, AZ, United States
Recall initiated2021-05-12
Classified2021-08-13
Reported by FDA2021-08-25
DistributedAZ, CA, DC, GA, IL, KY, MA, MD, NE, WA
Countries outside the USBR, CA, SA
Reason classeslabeling
UPC / GTIN / UDI-DI00733132606368, 00733132606375
Serial numbers6185496PP001, 6185502PP001, 6185502PP002, 6185502PP003, 6185502PP004, 6185502PP006, 6185502PP007, 6185502PP009, 6185502PP010, 6185503PP001, 6185503PP002, 6185503PP004, 6185503PP005, 6185503PP006, 6185503PP007, 6185503PP008, 6185503PP009, 6185503PP010, HPT060015, HPT060015A

Product

Gore Propaten Vascular Graft configured for Pediatric Shunt, Diameter 6 mm, Length 15 cm, Rx Only, Sterile EO, for the following Reference numbers: HPT060015 UDI: (01)00733132606368 HPT060015A UDI: (01)00733132606375

Reason for recall

Vascular Grafts containing an inner diameter of 6 mm may be incorrectly labeled as 5 mm and Vascular Grafts containing an inner diameter of 5 mm are incorrectly labeled as 6 mm.

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-2293-2021. 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.