CLASS II ONGOING Device recall · Reported 18 Mar 2026 · FDA Enforcement Report
Medline Unna-z Stretch Zinc Paste Bandage recalled by KOB
KOB is recalling Medline Unna-z Stretch Zinc Paste Bandage, distributed in Illinois. The recall was initiated on 15 Jan 2026 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1495-2026
- FDA event ID
- 98328
- Recalling firm
- KOB, Wolfstein, N/A
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 15 Jan 2026
- FDA classified
- 6 Mar 2026
- Reported
- 18 Mar 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Labeling Errors
- Device type
- Other Medical Devices
Timeline
| 15 Jan 2026 | Recall initiated by company | |
| 6 Mar 2026 | Classified by FDA | +50 days |
| 18 Mar 2026 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Due to labeling error. Incomplete ingredients listed. Labeling did not include castor oil or calamine.
Product as listed by the FDA
MEDLINE UNNA-Z STRETCH ZINC PASTE BANDAGE, REF NONUNNAS40 KOB article #40307010
Where it was distributed
U.S.: IL O.U.S.: Not provided as product is manufactured O.U.S.
Questions about this recall
Why was it recalled?
Due to labeling error. Incomplete ingredients listed. Labeling did not include castor oil or calamine.
Which lots are affected?
Model/Catalog Number: NONUNNAS40 KOB article #40307010 Customer Code: (01)10888277675438 Lot Numbers: 2520206 2520739
Where was it sold?
U.S.: IL O.U.S.: Not provided as product is manufactured O.U.S.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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