Dako Colorado, Inc. Eridan Automated Slide Stainer and Support Cart, REF E300 and E300SC1, Dako Colorado, Inc. (Catalog No. (ER 00130,00331,00230,00431) Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Eridan Automated Slide Stainer and Support Cart, REF E300 and E300SC1, Dako Colorado, Inc. (Catalog No. (ER 00130,00331,00230,00431)
Brand
Dako Colorado, Inc.
Lot Codes / Batch Numbers
Serial numbers: ER103, ER105, ER106, ER107, ER108, ER110, ER111, ER113, ER115, ER117, ER118.
Products Sold
Serial numbers: ER103, ER105, ER106, ER107, ER108, ER110, ER111, ER113, ER115, ER117, ER118.
Dako Colorado, Inc. is recalling Eridan Automated Slide Stainer and Support Cart, REF E300 and E300SC1, Dako Colorado, Inc. (Catalog due to Automated slide staining device may not stain speciman slides correctly, and therefore slides cannot be used for patient diagnosis.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Automated slide staining device may not stain speciman slides correctly, and therefore slides cannot be used for patient diagnosis.
Recommended Action
Per FDA guidance
Consignees were notified by phone on 10/02/2006 and later by letter on 10/20/2006. They were given the option of using the stainer as 'Research Use Only' or having the stainer returned to Dako.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, IN, NC, WA
Page updated: Jan 10, 2026