Port Access Infusion KIT - 1" Needle recall
PORT ACCESS INFUSION KIT - 1" NEEDLE Product Code: DYNDC2817
Why was Port Access Infusion KIT - 1" Needle recalled?
Supplier initiated recall of the GRIPPER Needles
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot Number Expiration 2019060390 11/30/2020
- Product
- PORT ACCESS INFUSION KIT - 1" NEEDLE Product Code: DYNDC2817
- Recalling firm
- Centurion Medical Products Corporation
- Quantity
- 200 kits
- Distribution
- IL
- Recall date
- November 6, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)