Diagnostica Stago Recalls

3 recalls found for Diagnostica Stago. Check if any of your products are affected.

Health & Personal Care
HIGH
FDA DEVICE

Diagnostica Stago Recalls Asserachrom HPIA Kit Over False Negatives

Diagnostica Stago issued a recall for 438 Asserachrom HPIA kits on December 15, 2025. The kits, used to detect PF4 antibodies, may produce false negative results. The affected lot is 271288, distributed worldwide including multiple U.S. states.

Diagnostica Stago
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Diagnostica Stago Recalls D-Dimer Test Due to Underestimation Risk

Diagnostica Stago recalled 12,740 D-Dimer testing devices on September 12, 2025. The recall follows a risk of underestimating D-Dimer levels in patients. Healthcare providers and patients should stop using the device immediately.

Diagnostica Stago
A potential
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Brand Statistics

Total Recalls
3
Pages
1