Recall Z-2620-2023— Copan Diagnostics Inc
Class II · Ongoing
Class II FDA medical device recall by Copan Diagnostics Inc, initiated 2023-07-14. FDA's recall record names no specific 510(k) clearance for this event. Product: COPAN REF: 2U045S01 300uL Transfer Pipette Individually wrapped pipettes, 1000 pcs.. Reason: Due to plastic defects, the pipette aspiration capability potentially doesn't meet the expected tolerance.
- Recalling firm
- Copan Diagnostics Inc
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2023-07-14
- Firm location
- Murrieta, CA, United States
Product description
COPAN REF: 2U045S01 300uL Transfer Pipette Individually wrapped pipettes, 1000 pcs.
Reason for recall
Due to plastic defects, the pipette aspiration capability potentially doesn't meet the expected tolerance
Data sourced from openFDA. This site is unofficial and independent of the FDA.