FDA Medical Device Recalls (openFDA)
Centurion Medical Products Corporation: EPISTAXIS TRAY Kit Code: MNS10165
- Recall number
- Z-0407-2020
- Recalling firm
- Centurion Medical Products Corporation
- Product
- EPISTAXIS TRAY Kit Code: MNS10165
- Status
- Terminated
- Initiated
- 2019-06-24
- Posted
- not on file
- Terminated
- 2020-07-24
- Reason
- Various medical device kits contain MAJOR Nasal Decongestant Spray is being recalled by the manufacturer
- Root cause
- Material/Component Contamination
- Action
- 1. Please identify all inventory that you have within your possession. Remove the MAJOR Nasal Decongestant from the mini-grip bag and segregate it in a location where it cannot be accessed for use. 2. Please complete the enclosed accountability record, whether or not you have product, and fax or email at your earliest convenience to the attention of Lisa Carpenter as directed. Upon receipt of this recall response, a Centurion Representative will contact you regarding retrieval of the product from your facility, if required. 3. please forward a copy of this notice to any facilities to whom this product may have been further distributed. If you have any questions, please contact (517) 546-5400 Ext 1122.
- Quantity
- 525 Kits
- Distribution
- CT, IL
- Lot, serial or model codes
- Lot # 2019051350 Exp 08/31/2020 Lot # 2019021501 Exp 04/30/2020 Lot # 2019010701 Exp 04/30/2020 Lot # 2018112601 Exp 04/30/2020 Lot # 2018092501 Exp 09/30/2019 Lot # 2018100201 Exp 09/30/2019 Lot # 2018062801 Exp 12/31/2019 Lot # 2018073101 Exp 09/30/2019 Lot # 2018042701 Exp 02/28/2019
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- OGR
- Firm FEI
- 3008403546
- Firm city
- Williamston
- 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