NEO Delta Selfsafe PUR T recall: Sterility Concern
NEO DELTA SELFSAFE PUR T, I.V. Catheter: a) REF 3738522 b) REF 3738822
Why was NEO Delta Selfsafe PUR T recalled?
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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?
a) REF 3738522, Lot 00A2160813 b) REF 3738822, Lot 00A1160822
- Product
- NEO DELTA SELFSAFE PUR T, I.V. Catheter: a) REF 3738522 b) REF 3738822
- Recalling firm
- Delta Med SpA
- Quantity
- 14,000 units
- Distribution
- US Nationwide distribution in the states of FL and MN.
- Recall date
- August 25, 2021
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)