MEDLINE UNNA-Z STRETCH ZINC PASTE BANDAGE, REF NONUNNAS40 KOB article #40307010
FDA Recall Z-1495-2026 · Posted 2026-03-06
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Recalling FirmKOB GmbH
Recall StatusOpen, Classified
Product CodeITG
Date Initiated2026-01-15
Product Quantity35,328
Reason for Recall
Due to labeling error. Incomplete ingredients listed. Labeling did not include castor oil or calamine.
Firm Action
On 01/15/2026, the firm sent a "Medical Device Recall" letter to its distributor informing them that product is being recalled due to a labeling error. The product box/package contained an incomplete ingredient statement. The ingredients castor oil and calamine were missing from the product labeling.
On 02/08/2026, the firm sent an updated "URGENT Medical Device Recall" Letter.
Customers are instructed to:
The products of the concerned lots must be scrapped. They shall not be used, distributed or made available on the market.
For questions or assistance - use email [email protected]
Root Cause
Packaging process control
Distribution Pattern
U.S.: IL O.U.S.: Not provided as product is manufactured O.U.S.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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