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GIARDIA/CRYPTOSPORIDIUM QUIK CHEK (2016-04-20)
- Starting date:
- April 20, 2016
- Posting date:
- May 16, 2016
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type III
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- Healthcare Professionals, General Public, Hospitals
- Identification number:
- RA-58380
Affected products
- GIARDIA/CRYPTOSPORIDIUM QUIK CHEK
Reason
One lot of membrane device components in Giardia/Cryptosporidium Quik Chek kits shipped between January 11, 2016 and February 24, 2016 may have been packaged in a foil pouch that identifies the product as C. DIFF QUIK CHEK. TECHLAB, Inc., the manufacturer of this product, has decided to take the precautionary measure of offering to replace any unused product. This notification affects only kit part number T30407, lot #1115114 and membrane devices, lot# 1115108.
Affected products
A. GIARDIA/CRYPTOSPORIDIUM QUIK CHEK
Lot or serial number
- 1115114
Model or catalog number
- T30407
Companies
- Manufacturer
-
TECHLAB INC.,
2001 KRAFT DRIVE
BLACKSBURG
24060-6358
Virginia
UNITED STATES