The CG+ Arrow PIC Catheters permit venous access to the central… — Class II medical device recall Z-1705-2017
Terminated recall by Arrow International Inc, reported 2017-04-12. Arrow International, Inc. notified its customers who received the affected Antimicrobial/Antithrombogenic PICC
| Recall number | Z-1705-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arrow International Inc, Reading, PA, United States |
| Recall initiated | 2017-03-03 |
| Classified | 2017-04-03 |
| Reported by FDA | 2017-04-12 |
| Terminated | 2018-02-27 |
| Quantity | 1,351 catheters |
| Reason classes | labeling |
| Lot numbers | 23F16A0727, 23F16C0844, 23F16C0851 |
Product
The CG+ Arrow PIC Catheters permit venous access to the central circulation through a peripheral vein.
Reason for recall
Arrow International, Inc. notified its customers who received the affected Antimicrobial/Antithrombogenic PICC Kits, that the kits were being recalled due to a labeling error. The lidstock on some of the kits reads CDC-45541-HPK1A, while the banner card on the side of the kit reads CDC-45052-HPK1A. Other kits may list CDC-45052-HPK1A on the lidstock and CDC-45541-HPK1A on the banner card. The affected lot numbers are 23F16C0851, 23F16A0727, and 23F16C0844.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1705-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.