Data Foundry

Medical device recalls 2021

Smart Port CT-Implantable Port Catalogue #: CT96STSD-VI — Class II medical device recall Z-1466-2021

Terminated recall by Angiodynamics Inc. (Navilyst Medical Inc.), reported 2021-04-28, distributed nationwide. AngioDynamics, Inc. is recalling a specific batch of AngioDynamics Implantable Infusion Port kits and Valved i

Recall numberZ-1466-2021
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmAngiodynamics Inc. (Navilyst Medical Inc.), Glens Falls, NY, United States
Recall initiated2021-02-22
Classified2021-04-21
Reported by FDA2021-04-28
Terminated2022-07-19
DistributedNationwide (US)
Quantity267 kits
Reason classessterility
Lot numbers5616651, 5647359, 5654129, 5654135, H787CT96STSAVI1
Model numbersCT96STSA-VI, CT96STSD-VI

Product

Smart Port CT-Implantable Port Catalogue #: CT96STSD-VI, CT96STSA-VI - Product Usage: indicated for any patient requiring repeated access of the vascular system, for delivery of medications, nutritional supplementation, fluids, blood, blood products, and sampling of blood and power injection of contrast media for imaging.

Reason for recall

AngioDynamics, Inc. is recalling a specific batch of AngioDynamics Implantable Infusion Port kits and Valved introducers that may have potential for compromised sterility of the device. Only the specific product/lot of the kit identified below is affected by this recall action. The Product Description, Product Number, Ref./Catalog Number and Batch/Lot number is provided below. No other products are affected by this recall.

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-1466-2021. 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.