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U.S. Department of Health and Human Services

Class 2 Device Recall Centurion Chest Tube Trays

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 Class 2 Device Recall Centurion Chest Tube Trayssee related information
Date Initiated by FirmDecember 11, 2019
Create DateFebruary 05, 2020
Recall Status1 Terminated 3 on September 04, 2020
Recall NumberZ-1043-2020
Recall Event ID 84530
Product Classification Thoracic catheter insertion tray - Product Code PYI
ProductCenturion 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
Code Information 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
Recalling Firm/
Manufacturer		 Centurion Medical Products Corporation
100 Centurion Way
Williamston MI 48895-9086
For Additional Information ContactSAME
517-546-5400
Manufacturer Reason
for Recall		Incomplete seals on the sterile package may compromise the sterility
FDA Determined
Cause 2		Packaging process control
ActionCenturion 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 in Commerce448
DistributionNationwide Foreign: GHANA
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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