Centurion- ENT SNUF3 SNUFFER KIT Y
This recall has been terminated (originally issued December 11, 2019).
- Recall Initiated
- December 11, 2019
- Terminated
- September 4, 2020
- Recall Number
- Z-1091-2020
- Quantity
- 146 units
- Firm Location
- Williamston, MI
- Official Source
- View on FDA website ↗
Reason for Recall
Incomplete seals on the sterile package may compromise the sterility
Distribution
Nationwide Foreign: GHANA
Lot / Code Info
Product/Description/Lot Numbers: SNUF3 SNUFFER KIT Y 2019011490
Root Cause
Packaging process control
Action Taken
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.