FDA Device recall Z-1100-2023
Precision Delivery Set with Filter, REF: PD06F
- FDA Device
- Class II
- ongoing
- Published 2023-02-15
On 2023-02-15 the FDA classified a Class II recall of Precision Delivery Set with Filter, REF: PD06F by Quest Medical, citing delivery Sets may have tubing that could become detached that could result in patient infection.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1100-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-12-23 |
| Published | 2023-02-15 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Quest Medical |
| Distribution | US |
Product
Precision Delivery Set with Filter, REF: PD06F; and Precision Delivery Set with Trifurcated Luer, REF: PDT05CV2
Reason
Delivery Sets may have tubing that could become detached that could result in patient infection.
Identifiers
| code_info | REF/UDI-DI/Lots (Expiration Dates): PD06F/00634624911062/65824 (4/18/2025), 65826 (4/18/2025), 66069 (5/16/2025); PDT05CV2/00634624921412/66645 (7/11/2025) |
|---|
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-1100-2023%22
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