Kit, Port Access recall
Kit, Port Access Product Code: DYNDC1582A
Why was Kit, Port Access 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 2018121350 8/31/2020 2019020750 9/30/2020 2019031550 4/30/2021 2019041550 4/30/2021 2019061750 1/31/2021 2019062450 4/30/2021
- Product
- Kit, Port Access Product Code: DYNDC1582A
- Recalling firm
- Centurion Medical Products Corporation
- Quantity
- 11260 kits
- Distribution
- IL
- Recall date
- November 6, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)