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Health product recall

Reuter Bobbin Vent Tubes and T-Tubes (2016-12-28)

Starting date:
December 28, 2016
Posting date:
January 18, 2017
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-61842

Affected Products

  1. Reuter Bobbin Vent Tubes
  2. T-Tubes

Reason

Boxes of 510-101 Lot 53226 and 500-101 Lot 53240 were packaged at the same time during final packaging. Final packaging consists of placing sealed sterile pouched tubes in boxes and labeling the boxes. Some of the final packed boxes had a mixture of these two tubes. All pouches were packaged and labeled correctly.

Affected products

A. Reuter Bobbin Vent Tubes

Lot or serial number

53240

Model or catalog number

500-101

Companies
Manufacturer

Grace Medical Inc.

8500 Wolf lake Drive, Suite 110

Memphis

38133

Tennessee

UNITED STATES


B. T-Tubes

Lot or serial number

53226

Model or catalog number

53226

Companies
Manufacturer

Grace Medical Inc.

8500 Wolf lake Drive, Suite 110

Memphis

38133

Tennessee

UNITED STATES