RecallRadar

FDA Device recall Z-2620-2023

COPAN REF: 2U045S01 300uL Transfer Pipette Individually wrapped pipettes, 1000 pcs

On 2023-09-27 the FDA classified a Class II recall of COPAN REF: 2U045S01 300uL Transfer Pipette Individually wrapped pipettes, 1000 pcs by Copan Diagnostics, citing due to plastic defects, the pipette aspiration capability potentially doesn't meet the expected tolerance.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2620-2023
ClassificationClass II
Statusongoing
Initiated2023-07-14
Published2023-09-27
Last updated2026-09-13 11:56 UTC
CompanyCopan Diagnostics
DistributionCA

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

Identifiers

code_info
UDI-50841467100545 / Lot Codes: B104661 B202918 B203404 B203405 B204186 B204187 B204819 B204820 B300133 B300410 B300608…UDI-50841467100545 / Lot Codes: B104661 B202918 B203404 B203405 B204186 B204187 B204819 B204820 B300133 B300410 B300608 B300647 B300679 B301129 B301133 B301135 B301134

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2620-2023%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.