Health product recall

Sodium Chloride 0.9% Inj 900mg/100ml USP (2018-05-11)

Starting date:
May 11, 2018
Type of communication:
Drug Recall
Subcategory:
Drugs
Hazard classification:
Type I
Source of recall:
Health Canada
Issue:
Product Safety
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-67478

Recalled Products

Sodium Chloride 0.9% Inj 900mg/100ml USP

Reason

Potential for leakage of the intravenous bag.

Depth of distribution

Wholesalers; Healthcare Establishments

Affected products

Sodium Chloride 0.9% Inj 900mg/100ml USP

DIN, NPN, DIN-HIM
DIN 00060208
Dosage form

Liquid

Strength

SODIUM CHLORIDE 900 MG / 100 ML

Lot or serial number

W8A17C1, W8B02C1, W8B09C1, W8C01C1, W8C01C1F, W8A19C1, W8A25C1, W8A29C1, W8B05C1, W8B05C1S, W8B13C1, W8B21C1, W8B26C1, W8C08C1, W8D13C1

Companies
Recalling Firm
Baxter Corporation
7125 Mississauga Road
Mississauga
L5N 0C2
CANADA
Marketing Authorization Holder
Baxter Corporation
7125 Mississauga Road
Mississauga
L5N 0C2
CANADA