FDA Medical Device Recalls (openFDA)
Centurion Medical Products Corporation: Centurion Chest Tube Trays: Kit Code Product CHT1170 CHEST TUBE TRAY CHT1700 CHEST TUBE INSERTION TRAY CHT1760 CHEST TRAY CHT275 CHEST TUBE INSERTION TRAY CHT440 CHEST TUBE INSERTION TRAY CHT701 CHEST TUBE INSERTION TRAY CHT760 CHEST TUBE INSERTION TRAY CHT940 CHEST TUBE INSERTION TRAY
- Recall number
- Z-1043-2020
- Recalling firm
- Centurion Medical Products Corporation
- Product
- Centurion Chest Tube Trays: Kit Code Product CHT1170 CHEST TUBE TRAY CHT1700 CHEST TUBE INSERTION TRAY CHT1760 CHEST TRAY CHT275 CHEST TUBE INSERTION TRAY CHT440 CHEST TUBE INSERTION TRAY CHT701 CHEST TUBE INSERTION TRAY CHT760 CHEST TUBE INSERTION TRAY CHT940 CHEST TUBE INSERTION TRAY
- Status
- Terminated
- Initiated
- 2019-12-11
- Posted
- not on file
- Terminated
- 2020-09-04
- Reason
- Incomplete seals on the sterile package may compromise the sterility
- Root cause
- Packaging process control
- Action
- Centurion issued a notification emailed to Medline Industries, Centurion's parent company. Centurion issued mailing letters via First Class Mail beginning on 12/12/2019, letter states reason for recall, health risk and action to take: Please identify all inventory that you have within your possession and segregate it in a location where it cannot be accessed for use. 2) If you have transferred possession of this product to another individual, to another department or to another location in your organization, you are required by FDA regulations to notify them of this recall communication. Please ask that any affected product be returned to you for collection. 3) Affected product is not to be returned to Centurion, and should be destroyed/discarded. Document the destruction of all product on the enclosed accountability record. 4) 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, Director of Quality Assurance Centurion Medical Products Corporation, (517) 546-5400 Ext.1122.
- Quantity
- 448
- Distribution
- Nationwide Foreign: GHANA
- Lot, serial or model codes
- Kit Code Product Lot Number CHT1170 CHEST TUBE TRAY 2019011690 CHT1700 CHEST TUBE INSERTION TRAY 2018111490 CHT1760 CHEST TRAY 2019031490 CHT275 CHEST TUBE INSERTION TRAY 2019050890 CHT440 CHEST TUBE INSERTION TRAY 2019050690 CHT701 CHEST TUBE INSERTION TRAY 2019012590 CHT760 CHEST TUBE INSERTION TRAY 2018110890 CHT940 CHEST TUBE INSERTION TRAY 2019010290
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- PYI
- 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