Alinity 09P2720Recalls & reported problems
Abbott GmbH · Alinity i Anti-CCP Reagent Kit 200 Tests · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Apr 24, 2025Open, Classified
transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
Z-1853-2025 · Root cause: Storage · FDA record ↗
Other ANTIBODIES, ANTI-CYCLIC CITRULLINATED PEPTIDE (CCP) devices
- BioPlex 2200 6653250Bio-Rad Laboratories, Inc. · ANTIBODIES, ANTI-CYCLIC CITRULLINATED PEPTIDE (CCP)1 recall1 report
- Phadia 2500EE 12-4100-02Phadia AB · ANTIBODIES, ANTI-CYCLIC CITRULLINATED PEPTIDE (CCP)1 recall0 reports
- IMMUNOSCAN CCPlus RA-96PLUSSvar Life Science AB · Antibodies, Anti-Cyclic Citrullinated Peptide (Ccp)1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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