FDA Medical Device Recalls (openFDA)
Richard-Allan Scientific Company: EZ Single Cytofunnel Brown, A78710004 Product Usage: The EZ Single Cytofunnel with Brown filter papter are intended for single use with the Thermo Scientific Cytospin.
- Recall number
- Z-2749-2018
- Recalling firm
- Richard-Allan Scientific Company
- Product
- EZ Single Cytofunnel Brown, A78710004 Product Usage: The EZ Single Cytofunnel with Brown filter papter are intended for single use with the Thermo Scientific Cytospin.
- Status
- Terminated
- Initiated
- 2018-06-04
- Posted
- not on file
- Terminated
- 2019-06-07
- Reason
- Mislabeled product
- Root cause
- Labeling mix-ups
- Action
- On June 4, 2018, ThermoFisher Scientific issued URGENT MEDICAL DEVICE RECALL notices to customers. Customers were advised to inspect stock, quarantine, safely dispose or return impacted product. Evidence of disposal is required to be sent to Thermo Shandon Limited. If affected product has been used with no issues, please notify Thermo Shandon Limited of the quantity that is unavailable for disposal. Complete and return the Recall Return Response Acknowledgement & Receipt form via email to marganne.miller@thermofisher.com
- Quantity
- 1,039 cases/40 boxes per case
- Distribution
- US Nationwide Distribution
- Lot, serial or model codes
- Lot # 17269A0
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- IFB
- Firm FEI
- 1831638
- Firm city
- Kalamazoo
- Firm state
- MI
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28