FDA Medical Device Recalls (openFDA)
Opgen Inc: CS011 GNR PNA FISH Control Slide, manufactured as a component of the CS011-10 GNR PNA FISH Control Slide kit . In-Vitro Diagnostic The CS011 GNR Traffic Light Control Slide provides a positive and negative control for the KT011 GNR Traffic Light PNA FISH kit. GNR Traffic Light PNA FISH provides rapid identification of E. coli, K. pneumoniae and P. aeruginosa directly from Gram-negative blood cultures
- Recall number
- Z-1328-2019
- Recalling firm
- Opgen Inc
- Product
- CS011 GNR PNA FISH Control Slide, manufactured as a component of the CS011-10 GNR PNA FISH Control Slide kit . In-Vitro Diagnostic The CS011 GNR Traffic Light Control Slide provides a positive and negative control for the KT011 GNR Traffic Light PNA FISH kit. GNR Traffic Light PNA FISH provides rapid identification of E. coli, K. pneumoniae and P. aeruginosa directly from Gram-negative blood cultures
- Status
- Terminated
- Initiated
- 2019-03-18
- Posted
- not on file
- Terminated
- 2019-08-05
- Reason
- May show diminished performance prior to its established expiration date resulting in an invalid control result for the KTOll GNR PNA FISH Test
- Root cause
- Under Investigation by firm
- Action
- OpGen issued recall letter via email on March 18, 2019. The notification provided reason for recall, health risk, and request to destroy any remaining inventory and return the completed Acknowledgement of Receipt of Notification Letter via OpGen, Inc., Attn: Autumn Collasius Regulatory Affairs,708 Quince Orchard Dr., Suite 205, Gaithersburg, MD 20878; Phone: 1 (301) 869-9683 Fax: 1 (301) 869-9684, e-mail: regulatory@opgen.com. The response form asks the customer to include how many of the affected slides they currently have in stock and how many they have already used. Questions or requests for further information, please contact OpGen Technical Support: US (Toll-Free): 1-866-376-0009 FAX: 1-301-869-9684 E-mail: techsupport@opgen.com
- Quantity
- 80 slides
- Distribution
- US Distribution to states of: CT, MI and VA.
- Lot, serial or model codes
- Lot Number FN80107
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- LJG
- Firm FEI
- 3007065145
- Firm city
- Gaithersburg
- Firm state
- MD
- 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