Data Foundry

Medical device recalls 2024

Synchro — Class II medical device recall Z-1909-2024

Ongoing recall by Stryker Neurovascular, reported 2024-06-05, distributed nationwide. Neurovascular devices did not meet the minimum sample size required for endotoxin testing during manufacturing

Recall numberZ-1909-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmStryker Neurovascular, Fremont, CA, United States
Recall initiated2024-04-23
Classified2024-05-28
Reported by FDA2024-06-05
DistributedNationwide (US)
Countries outside the USAE, AT, AU, BE, BR, CA, CH, CL, CN, CZ, DE, DK, ES, FI, FR, GB, HK, HU, IE, IL, IN, IT, JP, KR, LT, LU, NL, NO, PL, PT, RO, SA, SE, SG, SK, TH, TR, TW
Quantity2,859
Reason classessterility
UPC / GTIN / UDI-DI07613252186922, 07613252186946, 07613252187158, 07613252187165
Lot numbers123364, 123404, 123985, 124214, 124216
Model numbersM00313010, M00313310, M00316310, M00316330

Product

Synchro .014"guide wire, 35 cm tip, Catalog: M00313010 Synchro .014 guide wire, 300 cm length, Catalog: M00313310 SYNCHRO .010 WIRE SOFT STRAIGHT 200cm, Catalog: M00316310 SYNCHRO .010 WIRE SOFT STRAIGHT 300cm, Catalog: M00316330

Reason for recall

Neurovascular devices did not meet the minimum sample size required for endotoxin testing during manufacturing processes and are out of compliance with the AAMI ST72 standard, so these devices may exceed the acceptable limits of endotoxin levels; high levels of endotoxins may increase the risk of fever, shock and aseptic meningitis.

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-1909-2024. 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.