Z-0266-2020 Class II Terminated
FDA device recall Z-0266-2020 was initiated by Datascope Corp. on October 3, 2019 and is designated Class II. Reason for recall: One lot of "Low Level Output Cable - Interface to Philips Monitor" was received from the supplier with an incorrect cable in the packaging. The recall status is terminated (terminated January 8, 2021). Affected quantity: 7.
Recall Details
- Product Type
- Devices
- Report Date
- November 13, 2019
- Initiation Date
- October 3, 2019
- Termination Date
- January 8, 2021
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 7
Product Description
Low Level Output Cable Interface to Philips Monitor For Use With Cardiosave and CS300 Intra-Aortic Balloon Pumps (IABPs), Part Number 0012-00-1589-03
Reason for Recall
One lot of "Low Level Output Cable - Interface to Philips Monitor" was received from the supplier with an incorrect cable in the packaging.
Distribution Pattern
Distributed to CA, GA, and TX.
Code Information
10000493876