FDA Medical Device Recalls (openFDA)
Centurion Medical Products Corporation: PICC/Central Line Dressing Change Tray, DT14675, Sterile, Centurion Medical Products Corp., Williamston, MI. These kits are used for dressing changes.
- Recall number
- Z-1467-2011
- Recalling firm
- Centurion Medical Products Corporation
- Product
- PICC/Central Line Dressing Change Tray, DT14675, Sterile, Centurion Medical Products Corp., Williamston, MI. These kits are used for dressing changes.
- Status
- Terminated
- Initiated
- 2011-01-14
- Posted
- 2011-03-08
- Terminated
- 2011-06-21
- Reason
- The firm is conducting a subrecall of kits containing Triad Groups alcohol prep pads. Triad initiated a recall of prep pads due to a concern about potential contamination of the products with an objectional orgainism, Bacillus cereus.
- Root cause
- Nonconforming Material/Component
- Action
- The firm, Centurion Medical Products, sent an "URGENT PRODUCT RECALL NOTICE" dated January 12, 2011 to affected customers via Certified Mail, Return Receipt Requested. The notice described the product, problem and action to be taken. The customers were instructed to identify and remove all inventory of the recalled kits in their possession; forward a copy of this notice to any customers that this product was further distributed to, and complete and return the attached Accountability Record form via fax to 517-546-3356 or email to: lcarpenter@centurionmp.com. The notice states that a Centurion representative will contact them regarding retrieval of the product from the facility. Should your require additional information, please contact the Director of Quality Assurance & Regulatory Affairs at (517) 546-5400 ext. 1135.
- Quantity
- not on file
- Distribution
- Nationwide distribution: USA including state of: CT, ID, NM, MA, MO, MT, VA and SC.
- Lot, serial or model codes
- 2010030190, 2010020190, 2010010490.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- MCY
- 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