Data Foundry

Medical device recalls 2020

Plastic Cannula HOLDEX Item # 450216 — Class II medical device recall Z-2911-2020

Ongoing recall by C.A. Greiner & Sohne Gesellschaftmbh, reported 2020-09-09, distributed nationwide. Sample leaking from the sleeve covering the needle inside the cannula

Recall numberZ-2911-2020
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmC.A. Greiner & Sohne Gesellschaftmbh, Kremsmunster, N/A, Austria
Recall initiated2020-07-27
Classified2020-08-28
Reported by FDA2020-09-09
DistributedNationwide (US)
Quantity390,000 units
Reason classespackaging
Lot numbersA19073FK
Model numbers450216

Product

Plastic Cannula HOLDEX Item # 450216 - Product Usage: - Product Usage: It is intended for use in routine specimen withdrawal from specimen collection bags or bottles through needleless cannula ports.

Reason for recall

Sample leaking from the sleeve covering the needle inside the cannula

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-2911-2020. 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.