Copan Diagnostics Inc: Medical Device Recall in 2023 - (Recall #: Z-2620-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: July 14, 2023

Date Posted: September 27, 2023

Recall Number: Z-2620-2023

Event ID: 92832

Reason for Recall:

Due to plastic defects, the pipette aspiration capability potentially doesn't meet the expected tolerance

Status: Ongoing

Product Quantity: 2,592 units

Code Information:

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

Distribution Pattern:

US: CA OUS: None

Voluntary or Mandated:

Voluntary: Firm initiated