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