Health product recall

Alinity hq Analyzer, Alinity hs Slide Maker Stainer Module (2019-03-04)

Starting date:
March 4, 2019
Posting date:
June 14, 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-70217



Last updated: 2019-06-14

Affected Products

A. Alinity hq Analyzer

B. Alinity hs Slide Maker Stainer Module

Reason

Abbott has identified the safety interlock covering the septum piercing probes may not deploy when the bulk solution 1 Liter bottle is removed on the Alinity h-series: Alinity hq Analyzer & the Alinity hs Slide Maker Stainer Module.

Affected products

A. Alinity hq Analyzer

Lot or serial number

All serial numbers.

Model or catalog number

09P68-01

Companies
Manufacturer

Abbott GMBH & Co. K.G.

MAX PLANCK RING 2

WIESBADEN

65205

GERMANY


B. Alinity hs Slide Maker Stainer Module

Lot or serial number

All serial numbers.

Model or catalog number

09P69-01

Companies
Manufacturer

Abbott GMBH & Co. K.G.

MAX PLANCK RING 2

WIESBADEN

65205

GERMANY