FDA Device Recalls

Recalls /

#178728

Product

Centurion-Pitcher Kit GR100150ST GRADUATED PITCHER STERILE 1000 CC Y 2018121090 GR1200ST STERILE 1200CC PITCHER KIT Y 2019031990

FDA product code
KYWContainer, Liquid Medication, Graduated
Device class
Class 1
Medical specialty
General Hospital
Affected lot / code info
Product-Lot Code: GR100150ST GRADUATED PITCHER STERILE 1000 CC 2018121090 GR1200ST STERILE 1200CC PITCHER KIT 2019031990

Why it was recalled

Incomplete seals on the sterile package may compromise the sterility

Root cause (FDA determination)

Packaging process control

Action the firm took

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.

Recalling firm

Firm
Centurion Medical Products Corporation
Address
100 Centurion Way, Williamston, Michigan 48895-9086

Distribution

Distribution pattern
Nationwide Foreign: GHANA

Timeline

Recall initiated
2019-12-11
Terminated
2020-09-04
Status

Source: openFDA Device Recall endpoint. Recall record ID #178728. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.