Z-2303-2021 Class II Ongoing
FDA device recall Z-2303-2021 was initiated by Delta Med SpA on June 21, 2021 and is designated Class II. Reason for recall: Problems related to the sterilization of the medical devices; possible missing sterility of the medical device The recall status is ongoing. Affected quantity: 14,000 units.
Recall Details
- Product Type
- Devices
- Report Date
- August 25, 2021
- Initiation Date
- June 21, 2021
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 14,000 units
Product Description
NEO DELTA SELFSAFE PUR T, I.V. Catheter: a) REF 3738522 b) REF 3738822
Reason for Recall
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
Distribution Pattern
US Nationwide distribution in the states of FL and MN.
Code Information
a) REF 3738522, Lot 00A2160813 b) REF 3738822, Lot 00A1160822