Nussloch GmbH ASP6025 Tissue Processor — Class II medical device recall Z-2660-2017
Ongoing recall by Leica Microsystems, Inc., reported 2017-07-12, distributed in AR, AZ, CA, CT, DC, FL, GA, HI…. Incorrect labeling for specified voltage for the Alarm Connectors on the rear side of the unit.
| Recall number | Z-2660-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Leica Microsystems, Inc., Buffalo Grove, IL, United States |
| Recall initiated | 2017-06-19 |
| Classified | 2017-07-03 |
| Reported by FDA | 2017-07-12 |
| Distributed | AR, AZ, CA, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MN, MO, MT, NC, NE, NJ, NM, NV, NY, OH, PA, SC, TN, TX, UT, VA, WA, WI, WV |
| Countries outside the US | AE, AT, AU, BD, BE, BR, CA, CH, CL, CN, CO, CR, CZ, DE, ES, FR, GB, ID, IE, IL, IN, IT, JO, JP, KR, KW, LT, MA, MX, MY, NL, NO, PE, PH, PL, PT, QA, RO, RS, RU, SA, SG, SI, TH, TR, TW, ZA |
| Quantity | 812 units |
| Reason classes | labeling |
| Serial numbers | 200, 202, 204, 206, 208, 210, 212, 214, 216, 218, 220, 222, 224, 226, 228, 230, 232, 234, 238, 240, 242, 248, 250, 252, 254 and 180 more |
Product
Nussloch GmbH ASP6025 Tissue Processor
Reason for recall
Incorrect labeling for specified voltage for the Alarm Connectors on the rear side of the unit.
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-2660-2017. 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.