Health product recall

BD PCEA Administration Set (2020-04-08)

Starting date:
April 8, 2020
Posting date:
May 1, 2020
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-72933



Last updated: 2020-05-01

Affected Products

BD PCEA Administration Set

Reason

Recall is being initiated to notify customers that BD has discovered that specific lots of BD PCEA (Patient Controlled Epidural Analgesia) Administration sets have the potential to leak between the connection of the male luer and the yellow striped tubing. This leak may be observed while priming or during use.

Affected products

BD PCEA Administration Set

Lot or serial number
  • 18125862
  • 19015637
  • 19025228
  • 19025229
Model or catalog number
  • 30893-07
Companies
Manufacturer

BD Switzerland SARL

Route de Crassier 17, Business Park Terre Bonne

Eysins

1262

SWITZERLAND