FDA Device recall Z-1668-2022
DeRoyal Sterile Custom Kits containing ICU Medical MicroClave Clear Connectors
- FDA Device
- Class II
- terminated
- Published 2022-09-07
On 2022-09-07 the FDA classified a Class II recall of DeRoyal Sterile Custom Kits containing ICU Medical MicroClave Clear Connectors by Deroyal Industries, citing procedure packs contained a recalled product.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1668-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-08-12 |
| Published | 2022-09-07 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Deroyal Industries |
| Distribution | US |
Product
DeRoyal Sterile Custom Kits containing ICU Medical MicroClave Clear Connectors
Reason
Procedure packs contained a recalled product.
Identifiers
| code_info | NS CVR PREP PACK /89-6817.09; Lots 56391514 (exp 08/01/2023), 56926777 (exp 08/01/2023), 57103035 (exp. 08/01/2023); UD…NS CVR PREP PACK /89-6817.09; Lots 56391514 (exp 08/01/2023), 56926777 (exp 08/01/2023), 57103035 (exp. 08/01/2023); UDI-DI (GTIN): 00749756730938 NON-STERILE IR ADMISSION KIT / 89-8762.05; Lot 57104020 (exp 07/01/2023); UDI-DI (GTIN): 00749756883627 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1668-2022%22
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