Liquid Mouse Monoclonal Antibody CD15 — Class II medical device recall Z-1710-2014
Terminated recall by Leica Microsystems, Inc., reported 2014-06-11, distributed nationwide. Product does not function as intended up to the expiry date on the product labeling. There is a link between t
| Recall number | Z-1710-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Leica Microsystems, Inc., Buffalo Grove, IL, United States |
| Recall initiated | 2014-01-10 |
| Classified | 2014-06-03 |
| Reported by FDA | 2014-06-11 |
| Terminated | 2017-09-05 |
| Distributed | Nationwide (US) |
| Countries outside the US | AR, AU, BR, CO, GB, IT, MY, NG, NZ, PL, RO, RS, RU, SA, SE, TN, TR, TW, ZA |
| Quantity | 145 units |
| Reason classes | labeling |
| Lot numbers | 2014-03, 2014-08, 6015073, 6017936 |
Product
Liquid Mouse Monoclonal Antibody CD15 (NCL-L-CD15), a liquid tissue culture supernatant containing 15 mM sodium azide as a preservative. For in vitro diagnostic use.
Reason for recall
Product does not function as intended up to the expiry date on the product labeling. There is a link between the age of the product and staining intensity.
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-1710-2014. 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.