FDA Device recall Z-0352-2023
Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit, REF numbers: a) ASK-42703-NS, b) ASK-42703-PCCH2, c) ASK-42703-PUPM1, d) ASK-…
- FDA Device
- Class I
- terminated
- Published 2022-12-21
On 2022-12-21 the FDA classified a Class I recall of Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit, REF numbers: a) ASK-42703-NS, b) ASK-42703-PCCH2, c) ASK-42703-PUPM1, d) ASK-… by Arrow International, citing there is the potential for inadequate connection between the top and bottom housings of the Micro Clave Clear Connectors included in the Arrow MAC Two-Lumen Central Venous Access….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0352-2023 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2022-10-27 |
| Published | 2022-12-21 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Arrow International |
| Distribution | FL, GA, KY, OH, PA, WV |
Product
Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit, REF numbers: a) ASK-42703-NS, b) ASK-42703-PCCH2, c) ASK-42703-PUPM1, d) ASK-45703-NS, e) ASK-45703-PAU, f) ASK-45703-PCAM1, g) ASK-45703-PCCH2, h) ASK-45703-PN; catheter introducer
Reason
There is the potential for inadequate connection between the top and bottom housings of the Micro Clave Clear Connectors included in the Arrow MAC Two-Lumen Central Venous Access Kit and the Arrow Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit.
Identifiers
| code_info | a) ASK-42703-NS: UDI/DI 10801902162905, Lot Numbers: 13F22B0495 b) ASK-42703-PCCH2: UDI/DI 10801902141030, Lot Numbe…a) ASK-42703-NS: UDI/DI 10801902162905, Lot Numbers: 13F22B0495 b) ASK-42703-PCCH2: UDI/DI 10801902141030, Lot Numbers: 13F22C0862 c) ASK-42703-PUPM1: UDI/DI 10801902159592, Lot Numbers: 13F22B0021 d) ASK-45703-NS: UDI/DI 10801902162912, Lot Numbers: 13F22C0244 e) ASK-45703-PAU: UDI/DI 10801902159110, Lot Numbers: 13F22D0121 f) ASK-45703-PCAM1: UDI/DI 10801902203158, Lot Numbers: 13F22C0553 g) ASK-45703-PCCH2: UDI/DI 10801902141047, Lot Numbers: 13F22B0641 h) ASK-45703-PN: UDI/DI 10801902140675, Lot Numbers: 13F22C0350 |
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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-0352-2023%22
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