Health product recall

Alinity i and Alinity c Processing Module (2019-03-04)

Starting date:
March 4, 2019
Posting date:
March 15, 2019
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-69312

Affected Products

  1. Alinity c Processing Module
  2. Alinity i Processing Module

Reason

Abbott has identified that the safety interlock covering the septum piercing probes within the bulk solution bottle holder may not deploy when a bulk solution bottle is removed from the Alinity ci-series.

Affected products

A. Alinity c Processing Module

Lot or serial number

All serial numbers.

Model or catalog number

03R67-01

Companies
Manufacturer

Abbott GmbH and Co. K.G.

Max Planck Ring 2

Wiesbaden

65205

GERMANY

B. Alinity i Processing Module

Lot or serial number

All serial numbers.

Model or catalog number

03R65-01

Companies
Manufacturer

Abbott GmbH and Co. K.G.

Max Planck Ring 2

Wiesbaden

65205

GERMANY