Data Foundry

Medical device recalls 2017

Unna-Z — Class II medical device recall Z-1074-2017

Terminated recall by Medline Industries Inc, reported 2017-02-01, distributed nationwide. Medline Industries, Inc is recalling Unna Z Unna Boot Bandage 3X10 and Unna Z Unna Boot Bandage 4X10 due t

Recall numberZ-1074-2017
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmMedline Industries Inc, Mundelein, IL, United States
Recall initiated2016-11-23
Classified2017-01-23
Reported by FDA2017-02-01
Terminated2019-07-19
DistributedNationwide (US)
Countries outside the USCL, PE, SV, TW
Quantity117,059 units
Reason classesmicrobial contamination
Pathogensmold
Lot numbers52581

Product

Unna-Z, Unna Boot with Zinc and Calamine, Compression Wrap, 1 Per Box, 3-4in x 10yds

Reason for recall

Medline Industries, Inc is recalling Unna Z Unna Boot Bandage 3X10 and Unna Z Unna Boot Bandage 4X10 due to contamination of the products with common mold (Cladosporium sphaerospermum/cladosporioides/herbarum/phaenocomae/halotolerans and Penicillium corylophilum)..

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-1074-2017. 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.