Z-2305-2021 Class II Ongoing
FDA device recall Z-2305-2021 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: 40,000 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
- 40,000 units
Product Description
WOLF-PAK Self Safe Safety IV Catheter: a) REF PIVD2010W b) REF PIV2210W c) REF PIV2475W
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 PIVD2010W, Lot 1100256 b) REF PIV2210W, Lot 1100316 c) REF PIV2475W, Lot 1200084