SLIDERPREP PLUS SLIDE PREPARATION CENTRIFUGE — Class II medical device recall Z-1367-2013
Terminated recall by Separation Technology, Inc., reported 2013-05-29, distributed nationwide. Separation Technology, Inc. recalled SlidePrep Plus Cytology Centrifuges manufactured prior to January 1, 2013
| Recall number | Z-1367-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Separation Technology, Inc., Sanford, FL, United States |
| Recall initiated | 2013-03-13 |
| Classified | 2013-05-23 |
| Reported by FDA | 2013-05-29 |
| Terminated | 2013-12-24 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, TR |
| Quantity | 102 |
| Serial numbers | 0110, 0111, 0112, 0210, 0211, 0212, 0310, 0311, 0312, 0410, 0411, 0412, 0511, 0512, 0611, 0710, 0711, 0811, 0812, 0910, 0911, 0912, 1011, 1012, 1112 and 2 more |
Product
SLIDERPREP PLUS SLIDE PREPARATION CENTRIFUGE. Produce a monolayer of cells onto a glass slide from any fluid suspension.
Reason for recall
Separation Technology, Inc. recalled SlidePrep Plus Cytology Centrifuges manufactured prior to January 1, 2013 for having the potential to start up unexpectedly when encountering an electrostatic discharge.
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-1367-2013. 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.