Health product recall

Remel Fluid Thio Med (10ml) (2019-03-20)

Starting date:
March 20, 2019
Posting date:
April 5, 2019
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type III
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-69496

Last updated: 2019-04-05

Affected Products

Remel Fluid Thio Med (10ml)

Reason

This product may fail performance testing starting at 141 days after date of manufacture (Aug 15, 2018).

Affected products

Remel Fluid Thio Med (10ml)

Lot or serial number
  • 389375
Model or catalog number
  • R07172
Companies
Manufacturer
Remel Inc.
12076 Santa Fe Drive
Lenexa
66215
Kansas
UNITED STATES