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Health product recall

ACTIFUSE ABX(2015-08-19)

Starting date:
August 19, 2015
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type I
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-54738

Affected Products

  1. ACTIFUSE ABX

Reason

Baxter Corporation is issuing a recall of ACTIFUSE ABX products with expiry before 29th July 2017 due to the possibility that the products may have endotoxin levels above specification criteria.

Affected products

  1. ACTIFUSE ABX

Lot or serial number

>10 NUMBERS, CONTACT MFR

 

Model or catalog number
  • 506005078107
  • 506005078108
  • 506005078109
Companies
Manufacturer

Apatech Limited

370 Centennial Avenue,Centennial Park, Elstree

Herfordshire

UNITED KINGDOM