Arrow Pressure Injectable Arrowg+ard Blue Plus CVC Kit Recall: Inadequate Connector
Arrow recalls specific Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kits due to potential inadequate connection between Micro Clave Clear Connectors and the kit, which could lead to improper use.
Recall notice
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.
Contact the company
What happened, in plain English
Arrow is recalling certain Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kits because the Micro Clave Clear Connectors might not connect properly with the kit. This could lead to improper use during medical procedures. Read more at govinfonow.com/recall/59805-arrow-pressure-injectable-arrowg-ard-blue-plus-cvc-kit-recall.
Source Summary by GovInfoNow · govinfonow.com/recall/59805-arrow-pressure-injectable-arrowg-ard-blue-plus-cvc-kit-recall · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0352-2023
Cite this page
“Arrow Pressure Injectable Arrowg+ard Blue Plus CVC Kit Recall: Inadequate Connector.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/59805-arrow-pressure-injectable-arrowg-ard-blue-plus-cvc-kit-recall. Based on FDA recall #Z-0352-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0352-2023%22&limit=1).
Why it’s dangerous
The Micro Clave Clear Connectors included in the Arrow MAC Two-Lumen Central Venous Access Kit may not connect adequately with the Arrow Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit. This could lead to improper use during medical procedures, potentially causing complications.
Who’s affected
Healthcare professionals using the recalled CVC kits are most at risk. Patients receiving these kits may also be affected if the connectors fail to connect properly.
How to tell if you have this one
Check for the product's REF numbers: ASK-42703-NS, ASK-42703-PCCH2, ASK-42703-PUPM1, ASK-45703-NS, ASK-45703-PAU, ASK-45703-PCAM1, ASK-45703-PCCH2, or ASK-45703-PN. The kits also have specific lot numbers and UDI/DI codes listed in the recall notice.
- Brand
Arrow- Category
Medical device
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class I- Status
Terminated- Distribution
US Distributor in states of: FL, GA, KY, OH, PA and WV.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-0351-2023 | Arrow MAC Two-Lumen Central Venous Access Kit fr use with 7 - 7.5 Fr Catheters, REF ASK-11242-UPM1; catheter introducer; UDI/DI 10801902159448, Lot Number 13F22C0349 | 80 units |
| 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-45703-NS, e) ASK-45703-PAU, f) ASK-45703-PCAM1, g) ASK-45703-PCCH2, h) ASK-45703-PN; catheter introducer; 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 | 1275 units |
What to do — step by step
Check Product Details
Review the product's REF numbers and lot numbers to confirm if it is recalled.
Where it went and when
Where it was distributed
Distributed in 6 states.
FDA distribution: “US Distributor in states of: FL, GA, KY, OH, PA and WV.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Florida, Georgia, Kentucky, Ohio, Pennsylvania, West Virginia.
Recall timeline
FDA terminated this recall 23 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Similar recalls
Latest medical device recalls
Keep exploring
Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-0352-2023 (October 27, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0352-2023 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.