Quidel Cardiovascular, Inc.
Quidel Cardiovascular, Inc. holds FDA 510(k) medical device clearances, first cleared 2019, most recent 2020, with 2 FDA device recalls on record.
Top product codes for Quidel Cardiovascular, Inc.
FDA recalls by Quidel Cardiovascular, Inc.
- Z-1974-2023 — Quidel Triage Cardiac Panel: REF: 97000HS, 97021HS (Troponin I), 97022HS (CK-MB and Troponin I), 97000HSEU, 97000HSEUJP, 97000HZ01, 97000QIL. Lots T13664 - T14045.
- Z-1552-2020 — Quidel Triage TOX Drug Screen Control 1 Kit Box containing 5 Control 1 vials with 5 x 0.25 mL vials per box. Quidel Cardiovascular Inc. 9975 Summers Ridge Road San Diego, CA 92121 USA Quidel.com
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Quidel Cardiovascular, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.