Data Foundry

Medical device recalls 2016

BioFlo PICC with ENDEXO Technology Maximal Barrier Nursing Kit — Class II medical device recall Z-0709-2017

Terminated recall by Angiodynamics Inc. (Navilyst Medical Inc.), reported 2016-12-14, distributed nationwide. Medline Industries, Inc. supplies Navilyst with sterile package gloves included in the tandem packing of the M

Recall numberZ-0709-2017
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmAngiodynamics Inc. (Navilyst Medical Inc.), Glens Falls, NY, United States
Recall initiated2016-08-29
Classified2016-12-05
Reported by FDA2016-12-14
Terminated2018-06-15
DistributedNationwide (US)
Reason classeslabeling, sterility
Model numbers5018265, 5020644, 5024787, 5026458, 5026468

Product

BioFlo PICC with ENDEXO Technology Maximal Barrier Nursing Kit - 1) UPN # H965750121/Catalog No: 5018265, 2) UPN # H965750131/Catalog No:5024787, 3) UPN # H965750141/Catalog No: 5024787, 4) UPN # H965750241/Catalog No: 5020644, 5) UPN # H965750325/Catalog No: 5026458, 6) UPN # H965750355/Catalog No: 5026468 The BioFlo PICCs with ENDEXO Technology are indicated for short or long-term peripheral access to the central venous system for intravenous therapy, including but not limited to, the administration of fluids, medications, nutrients; the sampling of blood; for central venous pressure monitoring and for power injection of contrast media

Reason for recall

Medline Industries, Inc. supplies Navilyst with sterile package gloves included in the tandem packing of the Maximal Barrier Nursing Kits. Medline has determined that specific lots of the gloves supplied to Navilyst contain an incorrect expiration date. Navilyst has confirmed that Medlines affected sterile gloves (Medline Part Number MSG1075/MSG3075) have been included in a limited number of kits.

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-0709-2017. 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.