3M Coban Self-Adherent Wrap Shipper carton label identified the… — Class II medical device recall Z-0601-2016
Terminated recall by 3M Company - Health Care Business, reported 2016-01-13, distributed nationwide. Product mislabeled as latex free. Actual Catalog number 1581, lot 2020-10AN. contains latex. This could pose a
| Recall number | Z-0601-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | 3M Company - Health Care Business, Saint Paul, MN, United States |
| Recall initiated | 2015-12-01 |
| Classified | 2016-01-06 |
| Reported by FDA | 2016-01-13 |
| Terminated | 2016-05-24 |
| Distributed | Nationwide (US) |
| Reason classes | labeling |
| Lot numbers | 2018-10AM, 2018-AM, 2020-10AN |
| Model numbers | 1581, 2081 |
Product
3M Coban Self-Adherent Wrap Shipper carton label identified the product as 3M Coban LF Latex Free Catalog #2081, lot number 2018-10AM.
Reason for recall
Product mislabeled as latex free. Actual Catalog number 1581, lot 2020-10AN. contains latex. This could pose a health risk to users with sensitivity or allergic reaction to latex, which could range from mild to severe.
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-0601-2016. 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.