FDA Device recall Z-1568-2021
REF 20130-01 Spinning Spiros Closed Male Luer, Red Cap - Product Usage: provides access for the administration of fluids from a container t…
- FDA Device
- Class II
- ongoing
- Published 2021-05-19
On 2021-05-19 the FDA classified a Class II recall of REF 20130-01 Spinning Spiros Closed Male Luer, Red Cap - Product Usage: provides access for the administration of fluids from a container t… by Icu Medical, citing due to molding defect, there is a potential that certain lots of spinning and non-spinning Sprios male luers may exhibit small amounts of leakage in the inactivated position.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1568-2021 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2021-03-16 |
| Published | 2021-05-19 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Icu Medical |
| Distribution | US |
Product
REF 20130-01 Spinning Spiros Closed Male Luer, Red Cap - Product Usage: provides access for the administration of fluids from a container to a patients vascular system through the administration sets needle or catheter (which is inserted into a vein)
Reason
Due to molding defect, there is a potential that certain lots of spinning and non-spinning Sprios male luers may exhibit small amounts of leakage in the inactivated position.
Identifiers
| code_info | REF: 20130-01 UDI: (01) 1 0840619 02338 3 (17) 260101 (30) 50 (10) 5135750 (01) 1 0840619 02338 3 (17) 260101 (30…REF: 20130-01 UDI: (01) 1 0840619 02338 3 (17) 260101 (30) 50 (10) 5135750 (01) 1 0840619 02338 3 (17) 260101 (30) 50 (10) 5142982 Lot Number: 5135750 5142982 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1568-2021%22
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