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FDA Medical Device Recalls (openFDA)

Centurion Medical Products Corporation: PORT ACCESS INFUSION KIT - 1" NEEDLE Product Code: DYNDC2817

Recall number
Z-0256-2020
Recalling firm
Centurion Medical Products Corporation
Product
PORT ACCESS INFUSION KIT - 1" NEEDLE Product Code: DYNDC2817
Status
Terminated
Initiated
2019-07-15
Posted
not on file
Terminated
2020-08-31
Reason
Supplier initiated recall of the GRIPPER Needles
Root cause
Nonconforming Material/Component
Action
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.
Quantity
200 kits
Distribution
IL
Lot, serial or model codes
Lot Number Expiration 2019060390 11/30/2020
510(k) numbers
not on file
PMA numbers
not on file
Product code
OXQ
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

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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

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