Centurion Medical Products Corporation Kit, Port Access Product Code: DYNDC1582A Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Kit, Port Access Product Code: DYNDC1582A
Brand
Centurion Medical Products Corporation
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
Lot Number Expiration 2018121350 8/31/2020 2019020750 9/30/2020 2019031550 4/30/2021 2019041550 4/30/2021 2019061750 1/31/2021 2019062450 4/30/2021
Centurion Medical Products Corporation is recalling Kit, Port Access Product Code: DYNDC1582A due to Supplier initiated recall of the GRIPPER Needles. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Supplier initiated recall of the GRIPPER Needles
Recommended Action
Per FDA guidance
1. Please identify all inventory that you have within your possession and cease use immediately. 2. 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. Upon receipt of this record, Centurion Representative will contact you regarding retrieval of the product from your facility. 3. Please forward this recall information to any facilities to who this product may have been further distributed, instructing them to cease use immediately.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
IL
Page updated: Jan 10, 2026