ConvaTec, Inc: Medical Device Recall in 2017 - (Recall #: Z-2233-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Non-Rebreather Oxygen Mask, Adult High Concentration with 2.1 m (7) Oxygen Tubing, Product Code 108MM

Product Classification:

Class II

Date Initiated: May 10, 2017

Date Posted: June 14, 2017

Recall Number: Z-2233-2017

Event ID: 77282

Reason for Recall:

Status: Terminated

Product Quantity: N/A

Code Information:

Lot Number 100281, 100709, 100729, 101923, 103180, 103265, 103691, 103714, 104104, 105987, 110558

Distribution Pattern:

CA, CT, FL, GA, IL, MO, NJ, NY, NC, OH, PA, RI, VA , Puerto Rico, Australia, Belgium, Canada, Columbia, Czech, Denmark, Finland, France, Germany, Greece, Israel, Italy, Japan, Jordan, Malaysia, Malta, Netherlands, Norway, Rwanda, Saudi Arabia, Sweden, Switzerland, United Kingdom, and Vietnam

Voluntary or Mandated:

Voluntary: Firm initiated