FDA Device recall Z-2911-2020
Plastic Cannula HOLDEX Item # 450216 - Product Usage: - Product Usage: It is intended for use in routine specimen withdrawal from specimen…
- FDA Device
- Class II
- ongoing
- Published 2020-09-09
On 2020-09-09 the FDA classified a Class II recall of Plastic Cannula HOLDEX Item # 450216 - Product Usage: - Product Usage: It is intended for use in routine specimen withdrawal from specimen… by C A Greiner And Sohne Gesellschaftmbh, citing sample leaking from the sleeve covering the needle inside the cannula.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2911-2020 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2020-07-27 |
| Published | 2020-09-09 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | C A Greiner And Sohne Gesellschaftmbh |
| Distribution | US |
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
Sample leaking from the sleeve covering the needle inside the cannula
Identifiers
| code_info | Lot # A19073FK |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2911-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.