Lower riskMedical device recall · FDA · Published August 30, 2018
Medline Unna-Z Boot Wraps Recalled Due to Mold Risk
Medline recalls Unna-Z compression wraps with zinc oxide and calamine due to mold in specific lots. Affected items have item numbers NONUNNA3 or NONUNNA4 and certain lot numbers. Consumers should check their product details.
Firm received sporadic reports of discoloration on certain lots of the product, which has been identified as common mold.
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Contact the company
📍Recalling firmMEDLINE INDUSTRIES INC3 Lakes Dr · Northfield, IL 60093-2753
✎ GovInfoNow plain-language explainer
Medline is recalling Unna-Z boot compression wraps with zinc oxide and calamine that have specific item numbers and lot numbers. The product may contain mold, which could cause skin irritation or infection if the wrap is used. Read more at govinfonow.com/recall/69931-medline-unna-z-boot-wraps-recalled-due-to-mold-risk.
“Medline Unna-Z Boot Wraps Recalled Due to Mold Risk.” GovInfoNow, updated August 20, 2026. https://govinfonow.com/recall/69931-medline-unna-z-boot-wraps-recalled-due-to-mold-risk. Based on FDA recall #Z-0088-2019 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0088-2019%22&limit=1).
The FDA announced on 2018-08-30 that Medline Industries Inc voluntarily recalled Unna-Z Unna Boot Compression Wrap with Zinc Oxide and Calamine due to mold contamination. The recall affects 113,302 units distributed in the United States, Taiwan, and Chile.
How to tell if you have it
Brand: Medline
Product: Unna-Z: Unna Boot Compression Wrap with Zinc Oxide and Calamine
Item Numbers: NONUNNA3, NONUNNA4
Lot numbers (NONUNNA3): 70112, 70485, 70602, 80637, 80663, 80719
Lot numbers (NONUNNA4): 70182, 70593, 80638, 80644, 80660, 80709, 80712
The hazard
The firm received sporadic reports of discoloration on certain lots of the product, which has been identified as common mold.
Context
GovInfoNow's records show Medline Industries Inc has 48 other recalls on record since 2015-09-25. Other recent recalls include a 2022-07-21 Chest Tube Kit recall for non-sterile tape in a sterile component, a 2021-11-08 Hand Sanitizer Foam recall for leaking containers, and a 2021-10-27 Bedside PICC CDS Kit recall involving an expired NaCl bag. Other recent recalls of similar products include a 2026-08-11 Medline Convenience Kits Recall for fungal contamination risk, a 2026-07-20 Medline Convenience Kits Recall for risk of skin infection from open seal applicators, and a 2026-06-12 Medline Convenience Kits Recall for risk of microbial contamination from packaging wrinkles.
How to tell if you have this one
Check the item number on the packaging: NONUNNA3 or NONUNNA4. Look for specific lot numbers listed in the recall notice for each item number.
Brand
Medline
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Details
Identify the item number (NONUNNA3 or NONUNNA4) and lot number from the packaging to determine if your product is affected.
How this recall unfolded
Recall timeline
FDA terminated this recall 4.4 years after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The recall states that mold has been found in certain lots, but the product is generally safe if the mold is not present. Affected items should be checked for discoloration.
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-0088-2019 (August 30, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0088-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 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.