Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-T 5208 ECC SET, Part Number 701054588
Reported: June 13, 2018 Initiated: March 11, 2016 #Z-2104-2018
Product Description
Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-T 5208 ECC SET, Part Number 701054588
Reason for Recall
There is a potential problem with the cuvette where failure of the cuvette would cause an error message on the monitor display of H/S DISCONNECT AT CUVETTE.
Details
- Recalling Firm
- Datascope Corporation
- Units Affected
- 19 total kits
- Distribution
- The products were distributed to the following US states: AL, OR, and TX.
- Location
- Fairfield, NJ
Frequently Asked Questions
What product was recalled? ▼
Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-T 5208 ECC SET, Part Number 701054588. Recalled by Datascope Corporation. Units affected: 19 total kits.
Why was this product recalled? ▼
There is a potential problem with the cuvette where failure of the cuvette would cause an error message on the monitor display of H/S DISCONNECT AT CUVETTE.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 13, 2018. Severity: Low. Recall number: Z-2104-2018.
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